Year |
Citation |
Score |
2024 |
Wang Y, Xu T, Jin S, Wang JY, Yuan Q, Liu H, Tang Y, Zhang S, Li G. Design and Asymmetric Control of Orientational Chirality by using the Combination of C(sp2)-C(sp) Levers and Achiral N-Protecting Group. Chemistry (Weinheim An Der Bergstrasse, Germany). e202400005. PMID 38497560 DOI: 10.1002/chem.202400005 |
0.342 |
|
2024 |
Song ZJ, Bao Y, Sun YJ, Yan S, Zhang Y, Li G, Wang JY. Photoinduced Alkylsulfonylation and Cyanoalkylsulfonylation of Morita-Baylis-Hillman Adducts via Multicomponent Insertion of Sulfur Dioxide. The Journal of Organic Chemistry. PMID 38457276 DOI: 10.1021/acs.joc.4c00052 |
0.342 |
|
2024 |
Tang Y, Yuan Q, Zhang S, Wang JY, Surowiec K, Li G. Enantioselective synthesis of [1,1'-binaphthalene]-8,8'-diyl bis(diphenylphosphane) and its derivatives. Rsc Advances. 14: 2792-2795. PMID 38234866 DOI: 10.1039/d3ra07956b |
0.562 |
|
2023 |
Tang Y, Wang Y, Yuan Q, Zhang S, Wang JY, Jin S, Xu T, Pan J, Surowiec K, Li G. Aggregation-Induced Catalysis: Asymmetric Catalysis with Chiral Aggregates. Research (Washington, D.C.). 6: 0163. PMID 37303602 DOI: 10.34133/research.0163 |
0.574 |
|
2023 |
Wang JY, Zhang S, Yuan Q, Li G, Yan S. Catalytic Radical-Triggered Annulation/Iododifluoromethylation of Enynones for the Stereospecific Synthesis of 1-Indenones. The Journal of Organic Chemistry. PMID 37220028 DOI: 10.1021/acs.joc.3c00471 |
0.31 |
|
2023 |
Wang JY, Zhang S, Tang Y, Yan S, Li G. Copper-Catalyzed Annulation-Trifluoromethyl Functionalization of Enynones. Organic Letters. PMID 37010156 DOI: 10.1021/acs.orglett.3c00679 |
0.581 |
|
2023 |
Jin S, Xu T, Tang Y, Wang JY, Wang Y, Pan J, Zhang S, Yuan Q, Rahman AU, Aquino AJA, Lischka H, Li G. A new chiral phenomenon of orientational chirality, its synthetic control and computational study. Frontiers in Chemistry. 10: 1110240. PMID 36688043 DOI: 10.3389/fchem.2022.1110240 |
0.581 |
|
2022 |
Tang Y, Yuan Q, Wang Y, Zhang S, Wang JY, Jin S, Xu T, Pan J, Guilbeau CR, Pleasant AJ, Li G. Aggregation-induced polarization (AIP) of derivatives of BINOL and BINAP. Rsc Advances. 12: 29813-29817. PMID 36321081 DOI: 10.1039/d2ra05597j |
0.517 |
|
2022 |
Rouh H, Tang Y, Xu T, Yuan Q, Zhang S, Wang JY, Jin S, Wang Y, Pan J, Wood HL, McDonald JD, Li G. Aggregation-Induced Synthesis (AIS): Asymmetric Synthesis via Chiral Aggregates. Research (Washington, D.C.). 2022: 9865108. PMID 36061818 DOI: 10.34133/2022/9865108 |
0.808 |
|
2022 |
Tang Y, Zhang S, Xu T, Yuan Q, Wang JY, Jin S, Wang Y, Pan J, Griffin I, Chen D, Li G. Aggregation-Induced Polarization (): Optical Rotation Amplification and Adjustment of Chiral Aggregates of Folding Oligomers and Polymers. Frontiers in Chemistry. 10: 962638. PMID 36034657 DOI: 10.3389/fchem.2022.962638 |
0.541 |
|
2022 |
Tang Y, Wu G, Jin S, Liu Y, Ma L, Zhang S, Rouh H, Ali AIM, Wang JY, Xu T, Unruh D, Surowiec K, Li G. From Center-to-Multilayer Chirality: Asymmetric Synthesis of Multilayer Targets with Electron-Rich Bridges. The Journal of Organic Chemistry. PMID 35442684 DOI: 10.1021/acs.joc.2c00234 |
0.815 |
|
2022 |
Jin S, Wang JY, Tang Y, Rouh H, Zhang S, Xu T, Wang Y, Yuan Q, Chen D, Unruh D, Li G. Central-to-Folding Chirality Control: Asymmetric Synthesis of Multilayer 3D Targets With Electron-Deficient Bridges. Frontiers in Chemistry. 10: 860398. PMID 35433628 DOI: 10.3389/fchem.2022.860398 |
0.812 |
|
2022 |
Tang Y, Jin S, Zhang S, Wu GZ, Wang JY, Xu T, Wang Y, Unruh D, Surowiec K, Ma Y, Wang S, Katz C, Liang H, Li Y, Cong W, ... Li G, et al. Multilayer 3D Chiral Folding Polymers and Their Asymmetric Catalytic Assembly. Research (Washington, D.C.). 2022: 9847949. PMID 35265849 DOI: 10.34133/2022/9847949 |
0.574 |
|
2022 |
Wang JY, Tang Y, Wu GZ, Zhang S, Rouh H, Jin S, Xu T, Wang Y, Unruh D, Surowiec K, Ma Y, Li Y, Katz C, Liang H, Cong W, ... Li G, et al. Asymmetric Catalytic Assembly of Triple-Columned and Multilayered Chiral Folding Polymers Showing Aggregation-Induced Emission (AIE). Chemistry (Weinheim An Der Bergstrasse, Germany). e202200183. PMID 35092103 DOI: 10.1002/chem.202200183 |
0.799 |
|
2021 |
Rouh H, Tang Y, Zhang S, Ali AIM, Surowiec K, Unruh D, Li G. Asymmetric [4 + 2] cycloaddition synthesis of 4-chromene derivatives facilitated by group-assisted-purification (GAP) chemistry. Rsc Advances. 11: 39790-39796. PMID 35494146 DOI: 10.1039/d1ra08323f |
0.819 |
|
2021 |
Li G, Wang JY, Tang Y, Wu GZ, Zhang S, Rouh H, Xu T, Wang Y, Unruh D, Surowiec K, Ma Y. Asymmetric Catalytic Assembly of Triple-Columned and Multiple-Layered Chiral Folding Polymers Showing Aggregation-Induced Emission (AIE). Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 34962686 DOI: 10.1002/chem.202104102 |
0.788 |
|
2021 |
Rouh H, Tang Y, Zhang S, Ali AIM, Unruh D, Surowiec K, Li G. Asymmetric synthesis of functionalized 2,3-dihydrobenzofurans using salicyl -phosphonyl imines facilitated by group-assisted purification (GAP) chemistry. Organic & Biomolecular Chemistry. 19: 10319-10325. PMID 34812831 DOI: 10.1039/d1ob02078a |
0.815 |
|
2021 |
Wang JY, Li G, Hao WJ, Jiang B. Enantio- and Regioselective CuH-Catalyzed Conjugate Reduction of Yne-Allenones. Organic Letters. PMID 33955758 DOI: 10.1021/acs.orglett.1c00892 |
0.352 |
|
2021 |
Wu G, Liu Y, Rouh H, Ma L, Tang Y, Zhang S, Zhou P, Wang JY, Jin S, Unruh D, Surowiec K, Ma Y, Li G. Asymmetric Catalytic Approach to Multi-Layer 3D Chirality. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33931916 DOI: 10.1002/chem.202101318 |
0.787 |
|
2021 |
Li G, Wu G, Liu Y, Rouh H, Ma L, Tang Y, Zhang S, Zhou P, Wang JY, Jin S, Unruh D, Surowiec K, Ma Y. Asymmetric Catalytic Approach to Multi-Layer 3D Chirality. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33830589 DOI: 10.1002/chem.202100700 |
0.803 |
|
2021 |
Yang Z, Li P, Lu H, Li G. Copper-Catalyzed Asymmetric Borylacylation of Styrene and Indene Derivatives. The Journal of Organic Chemistry. PMID 33689325 DOI: 10.1021/acs.joc.1c00031 |
0.386 |
|
2021 |
Wu G, Liu Y, Yang Z, Ma L, Tang Y, Zhao X, Rouh H, Zheng Q, Zhou P, Wang JY, Siddique F, Zhang S, Jin S, Unruh D, Aquino AJA, ... ... Li G, et al. Triple-Columned and Multiple-Layered 3D Polymers: Design, Synthesis, Aggregation-Induced Emission (AIE), and Computational Study. Research (Washington, D.C.). 2021: 3565791. PMID 33629070 DOI: 10.34133/2021/3565791 |
0.772 |
|
2020 |
Wu G, Liu Y, Yang Z, Jiang T, Katakam N, Rouh H, Ma L, Tang Y, Ahmed S, Rahman AU, Huang H, Unruh D, Li G. Enantioselective assembly of multi-layer chirality. National Science Review. 7: 588-599. PMID 34692078 DOI: 10.1093/nsr/nwz203 |
0.798 |
|
2020 |
Zhang Y, Ge X, Lu H, Li G. Catalytic Decarboxylative C-N Formation to Generate Alkyl, Alkenyl and Aryl Amines. Angewandte Chemie (International Ed. in English). PMID 33026167 DOI: 10.1002/anie.202010974 |
0.369 |
|
2020 |
Dong X, Ma P, Zhang T, Jalani HB, Li G, Lu H. Iridium-Catalyzed C-H Amination of Weinreb Amides: A Facile Pathway toward Anilines and Quinazolin-2,4-diones. The Journal of Organic Chemistry. PMID 32969226 DOI: 10.1021/acs.joc.0c01789 |
0.353 |
|
2020 |
Rahman AU, Zarshad N, Zhou P, Yang W, Li G, Ali A. Hypervalent Iodine (III) Catalyzed Regio- and Diastereoselective Aminochlorination of Tailored Electron Deficient Olefins via GAP Chemistry. Frontiers in Chemistry. 8: 523. PMID 32733847 DOI: 10.3389/Fchem.2020.00523 |
0.426 |
|
2020 |
Wu Y, Chen K, Ge X, Ma P, Xu Z, Lu H, Li G. Redox-Neutral P(O)-N Coupling between P(O)-H Compounds and Azides via Dual Copper and Photoredox Catalysis. Organic Letters. PMID 32649207 DOI: 10.1021/Acs.Orglett.0C02207 |
0.378 |
|
2020 |
Liu X, Liu R, Qiu J, Cheng X, Li G. Chemical-Reductant-Free Electrochemical Deuteration Reaction using Deuterium Oxide. Angewandte Chemie (International Ed. in English). PMID 32394494 DOI: 10.1002/Anie.202005765 |
0.398 |
|
2020 |
Zhang TS, Hao WJ, Cai PJ, Li G, Tu SJ, Jiang B. Copper-Catalyzed Annulation-Cyanotrifluoromethylation of 1,6-Enynes Toward 1-Indanones via a Radical Process. Frontiers in Chemistry. 8: 234. PMID 32363174 DOI: 10.3389/Fchem.2020.00234 |
0.396 |
|
2020 |
Zhang S, Bedi D, Cheng LU, Unruh DK, Li G, Findlater M. Cobalt (II)-Catalyzed Stereoselective Olefin Isomerization: Facile Access to Acyclic Trisubstituted Alkenes. Journal of the American Chemical Society. PMID 32315519 DOI: 10.1021/Jacs.0C02101 |
0.473 |
|
2020 |
Zhang S, Li L, Li X, Zhang J, Xu K, Li G, Findlater M. Electroreductive 4-Pyridylation of Electron-deficient Alkenes with Assistance of Ni(acac). Organic Letters. PMID 32255638 DOI: 10.1021/Acs.Orglett.0C01014 |
0.32 |
|
2020 |
Fei H, Xu Z, Wu H, Zhu L, Jalani HB, Li G, Fu Y, Lu H. Stereospecific Electrophilic Fluorocyclization of α,β-Unsaturated Amides with Selectfluor. Organic Letters. PMID 32174122 DOI: 10.1021/Acs.Orglett.0C00620 |
0.414 |
|
2020 |
Liu Y, Ahmed S, Qin XY, Rouh H, Li G, Jiang B, Wu G. Synthesis of Diastereoenriched α-Aminomethyl Enaminones via A Brønsted Acid-Catalyzed Asymmetric aza-Baylis-Hillman Reaction of Chiral N-Phosphonyl Imines. Chemistry, An Asian Journal. PMID 32067345 DOI: 10.1002/Asia.201901734 |
0.826 |
|
2020 |
Wu G, Liu Y, Yang Z, Jiang T, Katakam N, Rouh H, Ma L, Tang Y, Ahmed S, Rahman AU, Huang H, Unruh D, Li G. Enantioselective assembly of multi-layer 3D chirality National Science Review. 7: 588-599. DOI: 10.1093/Nsr/Nwz203 |
0.349 |
|
2020 |
Liu Y, Wu G, Yang Z, Rouh H, Katakam N, Ahmed S, Unruh D, Cui Z, Lischka H, Li G. Multi-layer 3D chirality: new synthesis, AIE and computational studies Science China Chemistry. 63: 692-698. DOI: 10.1007/S11426-019-9711-X |
0.43 |
|
2020 |
Zhou P, Yang W, Li G, Hao W, Jiang B. Rh(III)‐Catalyzed [4 + 1] cyclization of Sulfoxonium Ylides and Anthranils for Accessing N‐Arylisatins Chemcatchem. DOI: 10.1002/Cctc.202000640 |
0.326 |
|
2019 |
Ge H, Li B, Lawrence B, Li G. Ligand-Controlled Direct γ-C-H Arylation of Aldehydes. Angewandte Chemie (International Ed. in English). PMID 31779049 DOI: 10.1002/Anie.201913126 |
0.406 |
|
2019 |
Zhou P, Yang WT, Rahman AU, Li G, Jiang B. Rh(III)-Catalyzed [3 + 3] Annulation Reaction of Cyclopropenones and Sulfoxonium Ylides toward Trisubstituted 2-Pyrones. The Journal of Organic Chemistry. PMID 31645097 DOI: 10.1021/Acs.Joc.9B02253 |
0.423 |
|
2019 |
Wu G, Liu Y, Yang Z, Katakam N, Rouh H, Ahmed S, Unruh D, Surowiec K, Li G. Multilayer Chirality and Its Synthetic Assembly. Research (Washington, D.C.). 2019: 6717104. PMID 31549078 DOI: 10.34133/2019/6717104 |
0.793 |
|
2019 |
Cai W, Wu J, Zhang H, Jalani HB, Li G, Lu H. Rh-Catalyzed Chemoselective [4+1] Cycloaddition Reaction towards Diverse 4-Methyleneprolines. The Journal of Organic Chemistry. PMID 31385501 DOI: 10.1021/Acs.Joc.9B01466 |
0.447 |
|
2019 |
Wu Y, Zhang Y, Jiang M, Dong X, Jalani HB, Li G, Lu H. Synergistic combination of visible-light photo-catalytic electron and energy transfer facilitating multicomponent synthesis of β-functionalized α,α-diarylethylamines. Chemical Communications (Cambridge, England). PMID 31094368 DOI: 10.1039/C9Cc02465D |
0.371 |
|
2019 |
Zhang T, Dong X, Jalani HB, Zou J, Li G, Lu H. Iridium-Catalyzed C-H Amination/Cyclization for Medium to Large N-Heterocycle-Fused Dihydroquinazolinones. Organic Letters. PMID 31042045 DOI: 10.1021/Acs.Orglett.9B01167 |
0.454 |
|
2019 |
Kattamuri PV, Yin J, Siriwongsup S, Kwon DH, Ess DH, Li Q, Li G, Yousufuddin M, Richardson PF, Sutton SC, Kürti L. Correction to "Practical Singly and Doubly Electrophilic Aminating Agents: A New, More Sustainable Platform for Carbon-Nitrogen Bond Formation". Journal of the American Chemical Society. PMID 30724562 DOI: 10.1021/Jacs.9B00398 |
0.3 |
|
2019 |
Zheng M, Li G, Lu H. Photoredox- or Metal-Catalyzed in Situ SO-Capture Reactions: Synthesis of β-Ketosulfones and Allylsulfones. Organic Letters. PMID 30698440 DOI: 10.1021/Acs.Orglett.9B00201 |
0.407 |
|
2019 |
Li G, D’Auria J, Katakam NK, Seifert CW. Efficient Synthesis of Methyl (S)-4-(1-Methylpyrrolidin-2-yl)-3-oxobutanoate as the Key Intermediate for Tropane Alkaloid Biosynthesis with Optically Active Form Heterocycles. 99: 604. DOI: 10.3987/Com-18-S(F)4 |
0.336 |
|
2019 |
Li G, Hao W, Hu J, Gao Y, Zhang W, Zhang K, Li W, Jiang B. Diastereoselective Synthesis of Poly-Substituted syn-Imidazolidine-2-thiones via Microwave-Assisted Three-Component [2+2+1] Heterocyclizations Heterocycles. 99: 267. DOI: 10.3987/Com-18-S(F)20 |
0.425 |
|
2019 |
Li Y, Qian F, Ge X, Liu T, Jalani HB, Lu H, Li G. Copper and cobalt co-catalyzed aerobic oxidative cross-dehydrogenative coupling reaction of (benzo)azoles Green Chemistry. 21: 5797-5802. DOI: 10.1039/C9Gc02464F |
0.365 |
|
2018 |
Li H, Hao WJ, Li G, Tu SJ, Jiang B. Fe(III)-Catalyzed Bicyclization of Yne-Allenones With Indoles for the Atom-Economic Synthesis of 3-Indolyl Cyclobutarenes. Frontiers in Chemistry. 6: 599. PMID 30564570 DOI: 10.3389/Fchem.2018.00599 |
0.411 |
|
2018 |
Li J, He L, Liu X, Cheng X, Li G. Electrochemical hydrogenation with gaseous ammonia. Angewandte Chemie (International Ed. in English). PMID 30549399 DOI: 10.1002/Anie.201813464 |
0.313 |
|
2018 |
Zheng MW, Yuan X, Cui YS, Qiu JK, Li G, Guo K. Electrochemical Sulfonylation/Heteroarylation of Alkenes via Distal Heteroaryl ipso-Migration. Organic Letters. PMID 30507201 DOI: 10.1021/Acs.Orglett.8B03191 |
0.386 |
|
2018 |
Rouh H, Liu Y, Katakam N, Pham L, Zhu YL, Li G. Synthesis of Functionalized Chromene and Chroman Derivatives via Cesium Carbonate Promoted Formal [4 + 2] Annulation of 2'-Hydroxychalcones with Allenoates. The Journal of Organic Chemistry. PMID 30481026 DOI: 10.1021/Acs.Joc.8B02627 |
0.801 |
|
2018 |
Dong X, Li Q, Li G, Lu H. Cobalt-Catalyzed Secondary Alkylation of Arenes and Olefins with Alkyl Ethers through the Cleavage of C(sp)-H and C(sp)-O Bonds. The Journal of Organic Chemistry. PMID 30351937 DOI: 10.1021/Acs.Joc.8B02197 |
0.368 |
|
2018 |
Liu X, Liu R, Dai J, Cheng X, Li G. Application of Hantzsch Ester and Meyer Nitrile in Radical Alkynylation Reactions. Organic Letters. PMID 30336057 DOI: 10.1021/Acs.Orglett.8B03050 |
0.376 |
|
2018 |
Zhang T, Hu X, Dong X, Li G, Lu H. Iridium-Catalyzed Unreactive C(sp)-H Amination with 2,2,2-Trichloroethoxycarbonyl Azide. Organic Letters. PMID 30232895 DOI: 10.1021/Acs.Orglett.8B02738 |
0.409 |
|
2018 |
Wang JY, Li MW, Li MF, Hao WJ, Li G, Tu SJ, Jiang B. N-Sulfonyl Bisimidazoline Ligands and Their Applications in Pd(II)-Catalyzed Asymmetric Addition toward α-Tertiary Amines. Organic Letters. PMID 30215527 DOI: 10.1021/Acs.Orglett.8B02374 |
0.377 |
|
2018 |
Huang MH, Hao WJ, Li G, Tu SJ, Jiang B. Recent advances in radical transformations of internal alkynes. Chemical Communications (Cambridge, England). PMID 30167626 DOI: 10.1039/C8Cc04618B |
0.312 |
|
2018 |
Zhang Y, Dong X, Wu Y, Li G, Lu H. Visible-Light-Induced Intramolecular C(sp)-H Amination and Aziridination of Azidoformates via a Triplet Nitrene Pathway. Organic Letters. PMID 30091932 DOI: 10.1021/Acs.Orglett.8B01980 |
0.382 |
|
2018 |
Yu M, Zhang T, Jalani HB, Dong X, Lu H, Li G. Iridium-Catalyzed Aryl C-H Sulfonamidation and Amide Formation Using a Bifunctional Nitrogen Source. Organic Letters. PMID 30085669 DOI: 10.1021/Acs.Orglett.8B01977 |
0.438 |
|
2018 |
Li H, Hao WJ, Wang M, Qin X, Tu SJ, Zhou P, Li G, Wang J, Jiang B. Catalytic Double [2 + 2] Cycloaddition Relay Enabled C-C Triple Bond Cleavage of Yne-Allenones. Organic Letters. PMID 29989832 DOI: 10.1021/Acs.Orglett.8B01841 |
0.405 |
|
2018 |
Cai W, Wang S, Jalani HB, Wu J, Lu H, Li G. Oxidative Cascade Reaction of N-Aryl-3-alkylideneazetidines and Carboxylic Acids: Access to Fused Pyridines. Organic Letters. PMID 29920103 DOI: 10.1021/Acs.Orglett.8B01427 |
0.406 |
|
2018 |
Li J, Huang W, Chen J, He L, Cheng X, Li G. Electrochemical Aziridination via Alkene Activation with a Sulfamate as Nitrogen Source. Angewandte Chemie (International Ed. in English). PMID 29624835 DOI: 10.1002/Anie.201801106 |
0.355 |
|
2018 |
Pan L, Yang K, Li G, Ge H. Palladium-catalyzed site-selective arylation of aliphatic ketones enabled by a transient ligand. Chemical Communications (Cambridge, England). PMID 29480302 DOI: 10.1039/C8Cc00980E |
0.351 |
|
2018 |
Yang L, Zhang Y, Zou X, Lu H, Li G. Visible-light-promoted intramolecular C–H amination in aqueous solution: synthesis of carbazoles Green Chemistry. 20: 1362-1366. DOI: 10.1039/C7Gc03392C |
0.375 |
|
2018 |
Qiu J, Hao W, Li G, Jiang B. Oxidative Catalytic Spiroketalization Leading to Diastereoselective Synthesis of Spiro[benzofuran‐2,1′‐isochromene]s Advanced Synthesis & Catalysis. 360: 1182-1192. DOI: 10.1002/Adsc.201701149 |
0.34 |
|
2017 |
Huang W, Chen J, Hong D, Chen W, Cheng X, Tian Y, Li G. Hydrophosphonodifluoromethylation of Alkenes via Thiyl-Radical/Photoredox Catalysis. The Journal of Organic Chemistry. PMID 29260876 DOI: 10.1021/Acs.Joc.7B02354 |
0.381 |
|
2017 |
Zhang H, Yang Z, Zhao BN, Li G. Group-Assisted Purification (GAP) chemistry for Asymmetric Mannich-type reaction of chiral N-phosphonyl imines with azlactones leading to syntheses of α-quaternary α, β-diamino acid derivatives. The Journal of Organic Chemistry. PMID 29235341 DOI: 10.1021/Acs.Joc.7B02556 |
0.495 |
|
2017 |
Zhou P, Wang JY, Zhang TS, Li G, Hao WJ, Tu SJ, Jiang B. Thiazolium salt-catalyzed C-C triple bond cleavage for accessing substituted 1-naphthols via benzannulation. Chemical Communications (Cambridge, England). PMID 29218334 DOI: 10.1039/C7Cc08792F |
0.369 |
|
2017 |
Wang JY, Zhou P, Li G, Hao WJ, Tu SJ, Jiang B. Synthesis of Functionalized Benzo[g]indoles and 1-Naphthols via Carbon-Carbon Triple Bond Breaking/Rearranging. Organic Letters. 19: 6682-6685. PMID 29189009 DOI: 10.1021/Acs.Orglett.7B03410 |
0.364 |
|
2017 |
Li Y, Qian F, Wang M, Lu H, Li G. Cobalt-Catalyzed Decarboxylative C-H (Hetero)Arylation for the Synthesis of Arylheteroarenes and Unsymmetrical Biheteroaryls. Organic Letters. PMID 28991486 DOI: 10.1021/Acs.Orglett.7B02730 |
0.442 |
|
2017 |
Fan W, Yang Z, Jiang B, Li G. I2-Catalyzed sulfenylation of indoles and pyrroles using triethylammonium thiolates as sulfenylating agents. Organic Chemistry Frontiers : An International Journal of Organic Chemistry. 4: 1091-1102. PMID 28983405 DOI: 10.1039/C6Qo00851H |
0.358 |
|
2017 |
Jiang B, Liu F, Wang JY, Zhou P, Li G, Hao WJ, Tu SJ. Merging [2 + 2] Cycloaddition with Radical 1,4-Addition: Metal-Free Access to Functionalized Cyclobuta[a]naphthalen-4-ols. Angewandte Chemie (International Ed. in English). PMID 28913917 DOI: 10.1002/Anie.201707615 |
0.387 |
|
2017 |
Liu S, Chen K, Lan XC, Hao WJ, Li G, Tu SJ, Jiang B. Synergistic silver/scandium catalysis for divergent synthesis of skeletally diverse chromene derivatives. Chemical Communications (Cambridge, England). PMID 28913519 DOI: 10.1039/C7Cc05563C |
0.444 |
|
2017 |
Li J, Zhang WW, Wei XJ, Hao WJ, Li G, Tu SJ, Jiang B. Synthesis of Tribenzo[b,e,g]phosphindole Oxides via Radical Bicyclization Cascades of o-Arylalkynylanilines. Organic Letters. PMID 28832169 DOI: 10.1021/Acs.Orglett.7B02071 |
0.376 |
|
2017 |
Li Q, Hu W, Hu R, Lu H, Li G. Cobalt-Catalyzed Cross-Dehydrogenative Coupling Reaction between Unactivated C(sp(2))-H and C(sp(3))-H Bonds. Organic Letters. PMID 28829611 DOI: 10.1021/Acs.Orglett.7B02316 |
0.374 |
|
2017 |
Fan W, Chen KY, Chen QP, Li G, Jiang B. Facile synthesis of benzo[b]thiophenes via metal-free radical-triggered intramolecular C-S bond formation. Organic & Biomolecular Chemistry. PMID 28745373 DOI: 10.1039/C7Ob01515A |
0.414 |
|
2017 |
Liu S, Lan XC, Chen K, Hao WJ, Li G, Tu SJ, Jiang B. Ag/Brønsted Acid Co-Catalyzed Spiroketalization of β-Alkynyl Ketones toward Spiro[chromane-2,1'-isochromene] Derivatives. Organic Letters. PMID 28696725 DOI: 10.1021/Acs.Orglett.7B01705 |
0.394 |
|
2017 |
Kattamuri PV, Yin J, Siriwongsup S, Kwon DH, Ess DH, Li Q, Li G, Yousufuddin M, Richardson PF, Sutton SC, Kürti L. Practical Singly and Doubly Electrophilic Aminating Agents: A New, More Sustainable Platform for Carbon-Nitrogen Bond-Formation. Journal of the American Chemical Society. PMID 28648054 DOI: 10.1021/Jacs.7B05279 |
0.396 |
|
2017 |
Li J, Zhang WW, Wei XJ, Liu F, Hao WJ, Wang SL, Li G, Tu SJ, Jiang B. Radical Deaminative ipso-Cyclization of 4-Methoxyanilines with 1,7-Enynes for Accessing Spirocyclohexadienone-Containing Cyclopenta[c]quinolin-4-ones. The Journal of Organic Chemistry. PMID 28594176 DOI: 10.1021/Acs.Joc.7B00704 |
0.439 |
|
2017 |
Zou X, Zou J, Yang L, Li G, Lu H. Thermal Rearrangement of Sulfamoyl Azides: Reactivity and Mechanistic Study. The Journal of Organic Chemistry. PMID 28414236 DOI: 10.1021/Acs.Joc.7B00308 |
0.354 |
|
2017 |
Wang L, Shi LX, Liu L, Li ZX, Xu T, Hao WJ, Li G, Tu SJ, Jiang B. Synthesis of Diastereoenriched Oxazolo[5,4-b]indoles via Catalyst-Free Multicomponent Bicyclizations. The Journal of Organic Chemistry. PMID 28296402 DOI: 10.1021/Acs.Joc.7B00129 |
0.389 |
|
2017 |
Wang AF, Zhou P, Zhu YL, Hao WJ, Li G, Tu SJ, Jiang B. Metal-free benzannulation of 1,7-diynes towards unexpected 1-aroyl-2-naphthaldehydes and their application in fused aza-heterocyclic synthesis. Chemical Communications (Cambridge, England). PMID 28265611 DOI: 10.1039/C7Cc00323D |
0.377 |
|
2017 |
Qiao S, Wilcox CB, Unruh DK, Jiang B, Li G. Asymmetric [3 + 2] Cycloaddition of Chiral N-Phosphonyl Imines with Methyl Isocyanoacetate for Accessing to 2-Imidazolines with Switchable Stereoselectivity. The Journal of Organic Chemistry. PMID 28249385 DOI: 10.1021/Acs.Joc.6B03068 |
0.468 |
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2017 |
Sun J, Qiu JK, Wu YN, Hao WJ, Guo C, Li G, Tu SJ, Jiang B. Silver-Mediated Radical C(sp(3))-H Biphosphinylation and Nitration of β-Alkynyl Ketones for Accessing Functional Isochromenes. Organic Letters. PMID 28157317 DOI: 10.1021/Acs.Orglett.6B03546 |
0.353 |
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2017 |
Qiao S, Mo J, Wilcox CB, Jiang B, Li G. Chiral GAP catalysts of phosphonylated imidazolidinones and their applications in asymmetric Diels-Alder and Friedel-Crafts reactions. Organic & Biomolecular Chemistry. PMID 28139798 DOI: 10.1039/C6Ob02801B |
0.444 |
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2017 |
Qiao S, Wu J, Mo J, Spigener PT, Zhao BN, Jiang B, Li G. Chiral Phosphinyl Enamines and Their Asymmetric Reduction through Group-Assisted Purification Chemistry Leading to Enantiopure β-Amino Esters/Amides Synlett. 28: 2483-2488. DOI: 10.1055/S-0036-1589080 |
0.422 |
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2017 |
Qiu J, Shan C, Wang D, Wei P, Jiang B, Tu S, Li G, Guo K. Metal‐Free Radical‐Triggered Selenosulfonation of 1,7‐Enynes for the Rapid Synthesis of 3,4‐Dihydroquinolin‐2(1H)‐ones in Batch and Flow Advanced Synthesis & Catalysis. 359: 4332-4339. DOI: 10.1002/Adsc.201701118 |
0.344 |
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2017 |
Wang D, Liu S, Lan X, Paniagua A, Hao W, Li G, Tu S, Jiang B. Tunable Dimerization and Trimerization of β‐Alkynyl Ketones via Silver Catalysis for Accessing Spiro and Dispiro Compounds Containing 1H‐Isochromene Advanced Synthesis & Catalysis. 359: 3186-3193. DOI: 10.1002/Adsc.201700543 |
0.427 |
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2016 |
Wu X, Miao J, Li Y, Li G, Ge H. Copper-promoted site-selective carbonylation of sp and sp C-H bonds with nitromethane. Chemical Science. 7: 5260-5264. PMID 30155175 DOI: 10.1039/C6Sc01087C |
0.312 |
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2016 |
Hao WJ, Zhou P, Wu FY, Jiang B, Tu SJ, Li G. New Three-Component Bicyclization Leading to Densely Functionalized Pyrazolo[3,4-d]thiazolo[3,2-a]pyrimidines. European Journal of Organic Chemistry. 2016: 1968-1971. PMID 28670172 DOI: 10.1002/Ejoc.201600163 |
0.427 |
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2016 |
Seifert CW, Paniagua A, White GA, Cai L, Li G. GAP Peptide Synthesis via Design of New GAP Protecting Group: An Fmoc/tBu Synthesis of Thymopentin Free from Polymers, Chromatography and Recrystallization. European Journal of Organic Chemistry. 2016: 1714-1719. PMID 28663711 DOI: 10.1002/Ejoc.201600026 |
0.36 |
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2016 |
Wu H, Yang B, Zhu L, Lu R, Li G, Lu H. High-Valent Palladium-Promoted Formal Wagner-Meerwein Rearrangement. Organic Letters. PMID 27796096 DOI: 10.1021/Acs.Orglett.6B02706 |
0.403 |
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2016 |
Hao WJ, Gao Q, Jiang B, Liu F, Wang SL, Tu SJ, Li G. Base-Promoted [4 + 1]/[3 + 1 + 1] Bicyclization of for Accessing Functionalized Indeno[1,2-c]furans. The Journal of Organic Chemistry. PMID 27792338 DOI: 10.1021/Acs.Joc.6B02249 |
0.372 |
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2016 |
Li Y, Wang M, Fan W, Qian F, Li G, Lu H. Cobalt-Catalyzed Cross-Dehydrogenative Coupling Reactions of (Benz)Oxazoles with Ethers. The Journal of Organic Chemistry. PMID 27787990 DOI: 10.1021/Acs.Joc.6B02211 |
0.412 |
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2016 |
Fan W, Li YR, Jiang B, Li G. Cascade bicyclization of triethylammonium thiolates with hydrazines: efficient access to pyrazolo[3,4-c]quinolines. Organic & Biomolecular Chemistry. 14: 9080-9087. PMID 27722433 DOI: 10.1039/C6Ob01728B |
0.417 |
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2016 |
Wu YN, Xu T, Fu R, Wang NN, Hao WJ, Wang SL, Li G, Tu SJ, Jiang B. Dual rhodium/copper catalysis: synthesis of benzo[b]fluorenes and 2-naphthalenylmethanones via de-diazotized cycloadditions. Chemical Communications (Cambridge, England). 52: 11943-11946. PMID 27722253 DOI: 10.1039/C6Cc06320A |
0.371 |
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2016 |
Li J, Chen J, Jiao W, Wang G, Li Y, Cheng X, Li G. Difluoroalkylation/C-H annulation cascade reaction induced by visible-light photoredox catalysis. The Journal of Organic Chemistry. PMID 27661095 DOI: 10.1021/Acs.Joc.6B01825 |
0.361 |
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2016 |
Yang K, Li Q, Liu Y, Li G, Ge H. Catalytic C-H Arylation of Aliphatic Aldehydes Enabled by a Transient Ligand. Journal of the American Chemical Society. PMID 27652493 DOI: 10.1021/Jacs.6B08478 |
0.381 |
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2016 |
Zhang TS, Xiong YJ, Hao WJ, Zhu XT, Wang SL, Li G, Tu SJ, Jiang B. DDQ-Mediated Three-Component Dioxygenation of Alkenes. The Journal of Organic Chemistry. PMID 27627443 DOI: 10.1021/Acs.Joc.6B01988 |
0.359 |
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2016 |
Chen W, Liu Z, Tian J, Li J, Ma J, Cheng X, Li G. Building Congested Ketone: Substituted Hantzsch Ester and Nitrile as Alkylation Reagents in Photoredox catalysis. Journal of the American Chemical Society. PMID 27622653 DOI: 10.1021/Jacs.6B06379 |
0.423 |
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2016 |
Cheng J, Deng X, Wang G, Li Y, Cheng X, Li G. Intermolecular C-H Quaternary Alkylation of Aniline Derivatives Induced by Visible-Light Photoredox Catalysis. Organic Letters. PMID 27571116 DOI: 10.1021/Acs.Orglett.6B02179 |
0.419 |
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2016 |
Zhang H, Yang B, Yang Z, Lu H, Li G. Asymmetric Synthesis of Chiral alpha-Methyl-alpha,beta-Diamino Acid Derivatives via Group-Assisted Purification (GAP) Chemistry Using N-Phosphonyl Imines and Ni(II)-Complexed Alanine Schiff Base. The Journal of Organic Chemistry. PMID 27459278 DOI: 10.1021/Acs.Joc.6B01385 |
0.396 |
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2016 |
Xie JB, Lin S, Qiao S, Li G. Asymmetric Catalytic Enantio- and Diastereoselective Boron Conjugate Addition Reactions of α-Functionalized α,β-Unsaturated Carbonyl Substrates. Organic Letters. PMID 27434500 DOI: 10.1021/Acs.Orglett.6B01998 |
0.392 |
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2016 |
Zhang TS, Hao WJ, Wang NN, Li G, Jiang DF, Tu SJ, Jiang B. Catalytic Oxidative Carbene Coupling of α-Diazo Carbonyls for the Synthesis of β-Amino Ketones via C(sp(3))-H Functionalization. Organic Letters. PMID 27305936 DOI: 10.1021/Acs.Orglett.6B01189 |
0.42 |
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2016 |
Li Q, Li Y, Hu W, Hu R, Li G, Lu H. Cobalt-Catalyzed C(sp2)-H Methylation Using Dicumyl Peroxide as both Methylating Reagent and Hydrogen Acceptor. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27272646 DOI: 10.1002/Chem.201602445 |
0.356 |
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2016 |
Yang B, Ji X, Xue Y, Zhang H, Shen M, Jiang B, Li G. Asymmetric aza-Morita-Baylis-Hillman reactions of chiral N-phosphonyl imines with acrylates via GAP chemistry/technology. Organic & Biomolecular Chemistry. PMID 27232108 DOI: 10.1039/C6Ob00847J |
0.497 |
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2016 |
Wu YN, Fu R, Wang NN, Hao WJ, Li G, Tu SJ, Jiang B. Catalytic Sulfur-Enabled Dehydrobicyclization of 1,6-Enynes toward Arylated Indeno[1,2-c]thiophenes. The Journal of Organic Chemistry. PMID 27176454 DOI: 10.1021/Acs.Joc.6B00692 |
0.366 |
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2016 |
Zhang T, Wang Z, Hu X, Yu M, Deng T, Li G, Lu H. Cesium Carboxylate-Promoted Iridium Catalyzed C-H Amidation/Cyclization with 2,2,2-Trichloroethoxycarbonyl Azide. The Journal of Organic Chemistry. PMID 27164005 DOI: 10.1021/Acs.Joc.6B00818 |
0.373 |
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2016 |
Hao WJ, Du Y, Wang D, Jiang B, Gao Q, Tu SJ, Li G. Catalytic Diazosulfonylation of Enynals toward Diazoindenes via Oxidative Radical-Triggered 5-exo-trig Carbocyclizations. Organic Letters. PMID 27028216 DOI: 10.1021/Acs.Orglett.6B00655 |
0.363 |
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2016 |
Wang NN, Hao WJ, Zhang TS, Li G, Wu YN, Tu SJ, Jiang B. Metal-free C(sp(3))-H functionalization: oxidative carbo-oxygenation of α-diazo carbonyls via radical dediazotization. Chemical Communications (Cambridge, England). PMID 26997205 DOI: 10.1039/C6Cc00816J |
0.369 |
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2016 |
Wang NN, Huang LR, Hao WJ, Zhang TS, Li G, Tu SJ, Jiang B. Synergistic Rhodium/Copper Catalysis: Synthesis of 1,3-Enynes and N-Aryl Enaminones. Organic Letters. 18: 1298-301. PMID 26987884 DOI: 10.1021/Acs.Orglett.6B00238 |
0.455 |
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2016 |
Ali MA, Yao X, Li G, Lu H. Rhodium-Catalyzed Selective Mono- and Diamination of Arenes with Single Directing Site "On Water". Organic Letters. PMID 26959640 DOI: 10.1021/Acs.Orglett.6B00318 |
0.362 |
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2016 |
Fan W, Li Q, Li Y, Sun H, Jiang B, Li G. I2/O2-Enabled N-S Bond Formation to Access Functionalized 1,2,3-Thiadiazoles. Organic Letters. PMID 26927417 DOI: 10.1021/Acs.Orglett.6B00079 |
0.411 |
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2016 |
Yang B, Shen M, Ji X, Xu Z, Sun H, Jiang B, Li G. Chiral N-Phosphonyl Imines for Aza-Morita-Baylis-Hillman Reaction via Group-Assisted Purification (GAP) Chemistry/Technology. The Journal of Organic Chemistry. PMID 26898573 DOI: 10.1021/Acs.Joc.6B00049 |
0.491 |
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2016 |
Li G, Dang Y, Sun M, Meng X, Zhao F, Hao W, Jiang B, Tu S. One-Pot Synthesis of Densely Functionalized Thiazoles and syn-3-Thioacrylates Heterocycles. 93: 529. DOI: 10.3987/Com-15-S(T)31 |
0.384 |
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2016 |
Fu R, Hao W, Wu Y, Wang N, Tu S, Li G, Jiang B. Sulfonyl radical-enabled 6-endo-trig cyclization for regiospecific synthesis of unsymmetrical diaryl sulfones Organic Chemistry Frontiers. 3: 1452-1456. DOI: 10.1039/C6Qo00422A |
0.404 |
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2016 |
Huang W, Chen W, Wang G, Li J, Cheng X, Li G. Thiyl-Radical-Catalyzed Photoreductive Hydrodifluoroacetamidation of Alkenes with Hantzsch Ester as a Multifunctional Reagent Acs Catalysis. 6: 7471-7474. DOI: 10.1021/Acscatal.6B02420 |
0.363 |
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2016 |
Qiao S, Pindi S, Spigener PT, Jiang B, Li G. Asymmetric synthesis of homoallylic amines via 1,2-addition of Grignard reagent to aliphatic N-phosphonyl hemiaminal Tetrahedron Letters. 57: 619-622. DOI: 10.1016/J.Tetlet.2015.12.106 |
0.518 |
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2016 |
Fan W, Li Y, Li Q, Jiang B, Li G. Domino reactions of cyclic enaminones leading to selective synthesis of pentacyclic indoles and its functionalization Tetrahedron. 72: 4867-4877. DOI: 10.1016/J.Tet.2016.06.058 |
0.44 |
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2016 |
Hao WJ, Zhou P, Wu FY, Jiang B, Tu SJ, Li G. Three-Component Bicyclization Leading to Densely Functionalized Pyrazolo[3,4-d]thiazolo[3,2-a]pyrimidines European Journal of Organic Chemistry. DOI: 10.1002/ejoc.201600163 |
0.319 |
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2016 |
Yang B, Shen M, Ji X, Xu Z, Sun H, Jiang B, Li G. ChemInform Abstract: Chiral N-Phosphonyl Imines for an Aza-Morita-Baylis-Hillman Reaction via Group-Assisted Purification (GAP) Chemistry. Cheminform. 47. DOI: 10.1002/CHIN.201631049 |
0.353 |
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2015 |
Wang AF, Zhu YL, Wang SL, Hao WJ, Li G, Tu SJ, Jiang B. Metal-Free Radical Haloazidation of Benzene-Tethered 1,7-Enynes Leading to Polyfunctionalized 3,4-Dihydroquinolin-2(1H)-ones. The Journal of Organic Chemistry. PMID 26716579 DOI: 10.1021/Acs.Joc.5B02655 |
0.374 |
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2015 |
Zhang T, Hu X, Wang Z, Yang TT, Sun H, Li G, Lu H. Carboxylate-assisted Iridium-Catalyzed C-H Amination of Arenes with Biologically Relevant Alkyl Azides. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26712274 DOI: 10.1002/Chem.201504880 |
0.445 |
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2015 |
Zhu YL, Jiang B, Hao WJ, Wang AF, Qiu JK, Wei P, Wang DC, Li G, Tu SJ. A new cascade halosulfonylation of 1,7-enynes toward 3,4-dihydroquinolin-2(1H)-ones via sulfonyl radical-triggered addition/6-exo-dig cyclization. Chemical Communications (Cambridge, England). PMID 26680370 DOI: 10.1039/C5Cc08895J |
0.387 |
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2015 |
Zhu YL, Jiang B, Hao WJ, Qiu JK, Sun J, Wang DC, Wei P, Wang AF, Li G, Tu SJ. Catalytic Arylsulfonyl Radical Triggered 1,7-Enyne Bicyclizations. Organic Letters. PMID 26618403 DOI: 10.1021/Acs.Orglett.5B03100 |
0.416 |
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2015 |
Gao Q, Hao WJ, Liu F, Tu SJ, Wang SL, Li G, Jiang B. Unexpected isocyanide-based three-component bicyclization for the stereoselective synthesis of densely functionalized pyrano[3,4-c]pyrroles. Chemical Communications (Cambridge, England). PMID 26576646 DOI: 10.1039/C5Cc08071A |
0.413 |
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2015 |
Chen ZZ, Liu S, Hao WJ, Xu G, Wu S, Miao JN, Jiang B, Wang SL, Tu SJ, Li G. Catalytic arylsulfonyl radical-triggered 1,5-enyne-bicyclizations and hydrosulfonylation of α,β-conjugates. Chemical Science (Royal Society of Chemistry : 2010). 6: 6654-6658. PMID 26568814 DOI: 10.1039/C5Sc02343B |
0.446 |
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2015 |
Yang K, Chen X, Wang Y, Li W, Kadi AA, Fun HK, Sun H, Zhang Y, Li G, Lu H. Cobalt-Catalyzed Decarboxylative 2-Benzoylation of Oxazoles and Thiazoles with alpha-Oxocarboxylic Acids. The Journal of Organic Chemistry. PMID 26449132 DOI: 10.1021/Acs.Joc.5B01450 |
0.384 |
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2015 |
Yang Z, Hao WJ, Wang SL, Zhang JP, Jiang B, Li G, Tu SJ. Synthesis of Allenyl Sulfones via a TBHP/TBAI-Mediated Reaction of Propargyl Alcohols with Sulfonyl Hydrazides. The Journal of Organic Chemistry. PMID 26280445 DOI: 10.1021/Acs.Joc.5B01684 |
0.415 |
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2015 |
Zhou P, Hao WJ, Zhang JP, Jiang B, Li G, Tu SJ. Cascade bicyclizations of o-alkynyl aldehydes with thiazolium salts: a new access toward poly-functionalized indeno[2,1-b]pyrroles. Chemical Communications (Cambridge, England). PMID 26178784 DOI: 10.1039/C5Cc04306A |
0.418 |
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2015 |
Qiu JK, Jiang B, Zhu YL, Hao WJ, Wang DC, Sun J, Wei P, Tu SJ, Li G. Catalytic Dual 1,1-H-Abstraction/Insertion for Domino Spirocyclizations. Journal of the American Chemical Society. PMID 26131954 DOI: 10.1021/Jacs.5B05735 |
0.412 |
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2015 |
Wu H, Zi W, Li G, Lu H, Toste FD. Gold(I)-Catalyzed Desymmetrization of 1,4-Dienes by an Enantioselective Tandem Alkoxylation/Claisen Rearrangement. Angewandte Chemie (International Ed. in English). PMID 26031403 DOI: 10.1002/Anie.201503357 |
0.453 |
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2015 |
Pan YY, Wu YN, Chen ZZ, Hao WJ, Li G, Tu SJ, Jiang B. Synthesis of 3-Iminoindol-2-amines and Cyclic Enaminones via Palladium-Catalyzed Isocyanide Insertion-Cyclization. The Journal of Organic Chemistry. 80: 5764-70. PMID 25919002 DOI: 10.1021/Acs.Joc.5B00727 |
0.419 |
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2015 |
Wu X, Yang K, Zhao Y, Sun H, Li G, Ge H. Cobalt-catalysed site-selective intra- and intermolecular dehydrogenative amination of unactivated sp(3) carbons. Nature Communications. 6: 6462. PMID 25753366 DOI: 10.1038/Ncomms7462 |
0.372 |
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2015 |
Yang Z, Hao WJ, Xu HW, Wang SL, Jiang B, Li G, Tu SJ. Base-promoted transannulation of heterocyclic enamines and 2,3-epoxypropan-1-ones: regio- and stereoselective synthesis of fused pyridines and pyrroles. The Journal of Organic Chemistry. 80: 2781-9. PMID 25692388 DOI: 10.1021/Acs.Joc.5B00067 |
0.429 |
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2015 |
An G, Seifert C, Li G. N-Phosphonyl/phosphinyl imines and group-assisted purification (GAP) chemistry/technology. Organic & Biomolecular Chemistry. 13: 1600-17. PMID 25523061 DOI: 10.1039/C4Ob02254H |
0.707 |
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2015 |
Yang Z, Jiang B, Hao WJ, Zhou P, Tu SJ, Li G. Synthesis of enaminones and their difluoroboron complexes through domino aryl migration. Chemical Communications (Cambridge, England). 51: 1267-70. PMID 25475958 DOI: 10.1039/C4Cc08257E |
0.41 |
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2015 |
Seifert CW, Pindi S, Li G. Asymmetric Carbamoyl Anion Additions to Chiral N-Phosphonyl Imines via the GAP Chemistry Process and Stereoselectivity Enrichments. The Journal of Organic Chemistry. 80: 447-52. PMID 25458404 DOI: 10.1021/Jo5024443 |
0.468 |
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2015 |
Li G, An G, Zhou W, Xu X, Pan Y. Solution-Phase-Peptide Synthesis without Purification of Column Chromatography and Recrystallization by Protecting Amino Acid Esters with Phosphinyl Chloride Heterocycles. 90: 1405. DOI: 10.3987/Com-14-S(K)99 |
0.664 |
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2015 |
An G, Seifert C, Sun H, Pan Y, Li G. Group-assisted purification (gap) for protection of amino acids using n-phosphonyl functional groups Heterocycles. 90: 344-356. DOI: 10.3987/Com-14-S(K)25 |
0.661 |
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2015 |
Li G, Jiang B, Tu S, Hao W, Fan W, Sun M, Ning Y. DOMINO [3+2+1] HETEROANNULATION FOR STEREOSELECTIVE SYNTHESIS OF ANTI-PYRAZOLO[3,4-d][1,3]OXAZINES Heterocycles. 91: 815-823. DOI: 10.3987/Com-14-13126 |
0.327 |
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2015 |
Xie J, Lin S, Luo J, Wu J, Winn TR, Li G. Asymmetric boron conjugate addition to α,β-unsaturated carbonyl compounds catalyzed by CuOTf/Josiphos under non-alkaline conditions Organic Chemistry Frontiers. 2: 42-46. DOI: 10.1039/C4Qo00271G |
0.443 |
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2015 |
Yang Z, Hao W, Xu H, Wang S, Jiang B, Li G, Tu S. ChemInform Abstract: Base-Promoted Transannulation of Heterocyclic Enamines and 2,3-Epoxypropan-1-ones: Regio- and Stereoselective Synthesis of Fused Pyridines and Pyrroles. Cheminform. 46: no-no. DOI: 10.1002/chin.201529209 |
0.33 |
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2014 |
Zhao J, Fang H, Han J, Pan Y, Li G. Metal-Free Preparation of Cycloalkyl Aryl Sulfides via Di-tert-butyl Peroxide-Promoted Oxidative C(sp3)[BOND]H Bond Thiolation of Cycloalkanes. Advanced Synthesis & Catalysis. 356: 2719-2724. PMID 25505857 DOI: 10.1002/Adsc.201400032 |
0.369 |
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2014 |
Tu XJ, Hao WJ, Ye Q, Wang SS, Jiang B, Li G, Tu SJ. Four-component bicyclization approaches to skeletally diverse pyrazolo[3,4-b]pyridine derivatives. The Journal of Organic Chemistry. 79: 11110-8. PMID 25338160 DOI: 10.1021/Jo502096T |
0.324 |
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2014 |
Xiong Y, Qian P, Cao C, Mei H, Han J, Li G, Pan Y. One-pot stereoselective synthesis of α,β-differentiated diamino esters via the sequence of aminochlorination, aziridination and intermolecular SN2 reaction. Beilstein Journal of Organic Chemistry. 10: 1802-7. PMID 25161740 DOI: 10.3762/Bjoc.10.189 |
0.454 |
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2014 |
Ma GH, Jiang B, Tu XJ, Ning Y, Tu SJ, Li G. Synthesis of isocoumarins with different substituted patterns via Passerini-aldol sequence. Organic Letters. 16: 4504-7. PMID 25140818 DOI: 10.1021/Ol502048E |
0.415 |
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2014 |
Jiang B, Tu XJ, Wang X, Tu SJ, Li G. Copper(I)-catalyzed multicomponent reaction providing a new access to fully substituted thiophene derivatives. Organic Letters. 16: 3656-9. PMID 24988049 DOI: 10.1021/Ol501404X |
0.444 |
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2014 |
Jiang B, Fan W, Sun MY, Ye Q, Wang SL, Tu SJ, Li G. Domino reaction of arylglyoxals with pyrazol-5-amines: selective access to pyrazolo-fused 1,7-naphthyridines, 1,3-diazocanes, and pyrroles. The Journal of Organic Chemistry. 79: 5258-68. PMID 24833111 DOI: 10.1021/Jo500823Z |
0.456 |
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2014 |
Xie JB, Luo J, Winn TR, Cordes DB, Li G. Group-assisted purification (GAP) chemistry for the synthesis of Velcade via asymmetric borylation of N-phosphinylimines. Beilstein Journal of Organic Chemistry. 10: 746-51. PMID 24778728 DOI: 10.3762/bjoc.10.69 |
0.408 |
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2014 |
Xiong Y, Mei H, Wu L, Han J, Pan Y, Li G. Synthesis of chiral N-phosphinyl α-imino esters and their application in asymmetric synthesis of α-amino esters by reduction. Beilstein Journal of Organic Chemistry. 10: 653-9. PMID 24778716 DOI: 10.3762/Bjoc.10.57 |
0.452 |
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2014 |
Jiang B, Ye Q, Fan W, Wang SL, Tu SJ, Li G. Four-component strategy for selective synthesis of azepino[5,4,3-cd]indoles and pyrazolo[3,4-b]pyridines. Chemical Communications (Cambridge, England). 50: 6108-11. PMID 24777181 DOI: 10.1039/C4Cc00740A |
0.342 |
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2014 |
Jiang B, Ning Y, Fan W, Tu SJ, Li G. Oxidative dehydrogenative couplings of pyrazol-5-amines selectively forming azopyrroles. The Journal of Organic Chemistry. 79: 4018-24. PMID 24731223 DOI: 10.1021/Jo5004967 |
0.379 |
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2014 |
Wu J, An G, Lin S, Xie J, Zhou W, Sun H, Pan Y, Li G. Solution-phase-peptide synthesis via the group-assisted purification (GAP) chemistry without using chromatography and recrystallization. Chemical Communications (Cambridge, England). 50: 1259-61. PMID 24336500 DOI: 10.1039/C3Cc48509A |
0.689 |
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2014 |
Zhang Y, Dai Y, Li G, Cheng X. The Catalytic Synthesis of Carboniolamide: The Role of sp3 Hybridized Oxygen Synlett. 25: 2644-2648. DOI: 10.1055/S-0034-1379101 |
0.382 |
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2014 |
Xiong Y, Mei H, Han J, Li G, Pan Y. Asymmetric synthesis of β′-amino-α,β-enones via addition of α,β-unsaturated ketone-derived enolates to chiral N-phosphonyl imines Tetrahedron Letters. 55: 2476-2479. DOI: 10.1016/J.Tetlet.2014.03.005 |
0.432 |
|
2013 |
Zhang JP, Fan W, Ding J, Jiang B, Tu SJ, Li G. REGIOSELECTIVE MULTICOMPONENT DOMINO REACTIONS PROVIDING RAPID AND EFFICIENT ROUTES TO FUSED ACRIDINES. Heterocycles. 88: 1065-1077. PMID 25364095 DOI: 10.3987/Com-13-S(S)65 |
0.451 |
|
2013 |
Sun H, Zhang H, Han J, Pan Y, Li G. Asymmetric C-C Bond Formation between Chiral N-Phosphonyl Imines and Ni(II)-Complex of Glycine Schiff Base Provides a GAP Synthesis of α,β-syn-Diamino Acid Derivatives. European Journal of Organic Chemistry. 2013: 4744-4747. PMID 25309122 DOI: 10.1002/Ejoc.201300554 |
0.476 |
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2013 |
Li TJ, Liu ZQ, Yin HM, Yao CS, Jiang B, Wang XS, Tu SJ, Li XL, Li G. Metal-free [3 + 2 + 1]/[2 + 2 + 1] biscyclization: stereospecific construction with concomitant functionalization of indolizin-5(1H)-one. The Journal of Organic Chemistry. 78: 11414-20. PMID 24168348 DOI: 10.1021/Jo401969G |
0.307 |
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2013 |
Xiong Y, Mei H, Xie C, Han J, Li G, Pan Y. Asymmetric synthesis of α-alkenyl homoallylic primary amines via 1,2-addition of Grignard reagent to α,β-unsaturated phosphonyl imines. Rsc Advances. 3: 15820-15826. PMID 24159373 DOI: 10.1039/C3Ra42927J |
0.434 |
|
2013 |
Kattamuri PV, Xiong Y, Pan Y, Li G. N,N-DIIsopropyl-N-phosphonyl imines lead to efficient asymmetric synthesis of aziridine-2-carboxylic esters. Organic & Biomolecular Chemistry. 11: 3400-8. PMID 23563304 DOI: 10.1039/C3Ob40251G |
0.461 |
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2013 |
Jiang B, Wang X, Xu HW, Tu MS, Tu SJ, Li G. Highly selective domino multicyclizations for forming polycyclic fused acridines and azaheterocyclic skeletons. Organic Letters. 15: 1540-3. PMID 23506186 DOI: 10.1021/Ol400322V |
0.43 |
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2013 |
Pindi S, Wu J, Li G. Design, synthesis, and applications of chiral N-2-phenyl-2-propyl sulfinyl imines for group-assisted purification (GAP) asymmetric synthesis. The Journal of Organic Chemistry. 78: 4006-12. PMID 23496279 DOI: 10.1021/Jo400354R |
0.502 |
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2013 |
Hu FL, Wei Y, Shi M, Pindi S, Li G. Asymmetric catalytic aza-Morita-Baylis-Hillman reaction for the synthesis of 3-substituted-3-aminooxindoles with chiral quaternary carbon centers. Organic & Biomolecular Chemistry. 11: 1921-4. PMID 23407608 DOI: 10.1039/C3Ob27495K |
0.495 |
|
2013 |
Sun H, Han J, Kattamuri PV, Pan Y, Li G. Approach to vicinal t-Boc-amino dibromides via catalytic aminobromination of nitrostyrenes without using chromatography and recrystallization. The Journal of Organic Chemistry. 78: 1171-5. PMID 23311641 DOI: 10.1021/Jo302727V |
0.38 |
|
2013 |
Zhao J, Zhou W, Han J, Li G, Pan Y. Iron-catalyzed alkenylation of cyclic ethers via decarboxylative sp3(C)–sp2(C) coupling Tetrahedron Letters. 54: 6507-6510. DOI: 10.1016/J.Tetlet.2013.09.082 |
0.377 |
|
2013 |
Chen S, Han J, Li G, Pan Y. Highly diastereoselective aminobromination of β-methyl-β-nitrostyrenes with t-butyl N,N-dibromocarbamate/t-butyl carbamate as bromine/nitrogen sources Tetrahedron Letters. 54: 2781-2784. DOI: 10.1016/J.Tetlet.2013.02.113 |
0.345 |
|
2013 |
Zhao J, Fang H, Xie C, Han J, Li G, Pan Y. Palladium-Catalyzed C3 Acylation of Benzofurans and Benzothiophenes with Aromatic Aldehydes by Cross-Dehydrogenative Coupling Reactions Asian Journal of Organic Chemistry. 2: 1044-1047. DOI: 10.1002/Ajoc.201300208 |
0.395 |
|
2013 |
Shi F, Tan W, Zhang H, Li M, Ye Q, Ma G, Tu S, Li G. Asymmetric Organocatalytic Tandem Cyclization/Transfer Hydrogenation: A Synthetic Strategy for Enantioenriched Nitrogen Heterocycles Advanced Synthesis & Catalysis. 355: 3715-3726. DOI: 10.1002/Adsc.201300576 |
0.343 |
|
2012 |
Li TJ, Yin HM, Yao CS, Wang XS, Jiang B, Tu SJ, Li G. A one-pot multicomponent strategy for stereospecific construction of tricyclic pyrrolo[1,2-a]quinolines. Chemical Communications (Cambridge, England). 48: 11966-8. PMID 23128187 DOI: 10.1039/C2Cc37066B |
0.403 |
|
2012 |
Yuan W, Dong X, Shi M, McDowell P, Li G. Rh(I)-catalyzed Pauson-Khand-type cycloaddition reaction of ene-vinylidenecyclopropanes with carbon monoxide (CO). Organic Letters. 14: 5582-5. PMID 23098194 DOI: 10.1021/Ol302705Z |
0.44 |
|
2012 |
Jiang B, Li QY, Tu SJ, Li G. Three-component domino reactions for selective formation of indeno[1,2-b]indole derivatives. Organic Letters. 14: 5210-3. PMID 23025431 DOI: 10.1021/Ol3023038 |
0.431 |
|
2012 |
Jiang B, Li Y, Tu MS, Wang SL, Tu SJ, Li G. Allylic amination and N-arylation-based domino reactions providing rapid three-component strategies to fused pyrroles with different substituted patterns. The Journal of Organic Chemistry. 77: 7497-505. PMID 22852549 DOI: 10.1021/Jo301323R |
0.453 |
|
2012 |
Jiang B, Feng BM, Wang SL, Tu SJ, Li G. Domino constructions of pentacyclic indeno[2,1-c]quinolines and pyrano[4,3-b]oxepines by [4+1]/[3+2+1]/[5+1] and [4+3] multiple cyclizations. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 9823-6. PMID 22767331 DOI: 10.1002/Chem.201201109 |
0.388 |
|
2012 |
Yuan Z, Mei L, Wei Y, Shi M, Kattamuri PV, McDowell P, Li G. Asymmetric catalytic Mannich-type reaction of hydrazones with difluoroenoxysilanes using imidazoline-anchored phosphine ligand-zinc(II) complexes. Organic & Biomolecular Chemistry. 10: 2509-13. PMID 22334290 DOI: 10.1039/C2Ob07022G |
0.41 |
|
2012 |
Jiang B, Li QY, Zhang H, Tu SJ, Pindi S, Li G. Efficient domino approaches to multifunctionalized fused pyrroles and dibenzo[b,e][1,4]diazepin-1-ones. Organic Letters. 14: 700-3. PMID 22260312 DOI: 10.1021/Ol203166C |
0.356 |
|
2012 |
Jiang B, Yi MS, Shi F, Tu SJ, Pindi S, McDowell P, Li G. A multi-component domino reaction for the direct access to polyfunctionalized indoles via intermolecular allylic esterification and indolation. Chemical Communications (Cambridge, England). 48: 808-10. PMID 22038299 DOI: 10.1039/C1Cc15913E |
0.42 |
|
2012 |
Wang Q, Dai AX, Yi MS, Jiang B, Tu SJ, Li G. Highly stereoselective synthesis of anti-tetrahydropyrimidine derivatives under microwave heating Heterocycles. 86: 411-424. DOI: 10.3987/Com-12-S(N)40 |
0.449 |
|
2012 |
Li G, Tu S, Jiang B, Ma N, Wang X. MICROWAVE-ASSISTED MULTICOMPONENT REACTION IN WATER : HIGHLY STEREOSELECTIVE SYNTHESIS OF PYRIMIDINESPIROISOXAZOLO〔5,4-b〕PYRIDINE DERIVATIVES (Dedicated to Dr. Albert Padwa on his 75th birthday) Heterocycles. 84: 765-774. DOI: 10.3987/Com-11-S(P)53 |
0.386 |
|
2012 |
Ji X, Duan Z, Qian Y, Han J, Li G, Pan Y. Highly regioselective aminobromination of α,β-unsaturated nitro compounds with benzyl carbamate/N-bromosuccinimide as nitrogen/bromine source Rsc Advances. 2: 5565. DOI: 10.1039/C2Ra20490H |
0.427 |
|
2012 |
Mei H, Xiong Y, Qian Y, Han J, Li G, Pan Y. Na3PO4-catalyzed aminochlorination reaction of β-nitrostyrenes in water Rsc Advances. 2: 151-155. DOI: 10.1039/C1Ra00679G |
0.343 |
|
2012 |
Qian Y, Ji X, Zhou W, Han J, Li G, Pan Y. Aminochlorination reaction with N-chlorophthalimide as a new nitrogen/chlorine source resulting in α-amino derivatives Tetrahedron. 68: 6198-6203. DOI: 10.1016/J.Tet.2012.05.066 |
0.41 |
|
2011 |
Wang SL, Cheng C, Wu FY, Jiang B, Shi F, Tu SJ, Rajale T, Li G. Microwave-assisted multicomponent reaction in water leading to highly regioselective formation of benzo[f]azulen-1-ones. Tetrahedron. 67: 4485-4493. PMID 21731115 DOI: 10.1016/J.Tet.2011.05.002 |
0.418 |
|
2011 |
Jiang B, Wang X, Shi F, Tu SJ, Li G. New multicomponent cyclization: domino synthesis of pentasubstituted pyridines under solvent-free conditions. Organic & Biomolecular Chemistry. 9: 4025-8. PMID 21523293 DOI: 10.1039/C0Ob01258K |
0.464 |
|
2011 |
Liu Z, Gu P, Shi M, McDowell P, Li G. Catalytic asymmetric addition of arylboronic acids to isatins using C2-symmetric cationic N-heterocyclic carbenes (NHCs) Pd2+ diaqua complexes as catalysts. Organic Letters. 13: 2314-7. PMID 21452826 DOI: 10.1021/Ol200566S |
0.421 |
|
2011 |
Jiang B, Zhang G, Ma N, Shi F, Tu SJ, Kaur P, Li G. A new rapid multicomponent domino reaction for the formation of functionalized benzo[h]pyrazolo[3,4-b]quinolines. Organic & Biomolecular Chemistry. 9: 3834-8. PMID 21445382 DOI: 10.1039/C1Ob05034F |
0.426 |
|
2011 |
Kattamuri PV, Ai T, Pindi S, Sun Y, Gu P, Shi M, Li G. Asymmetric synthesis of α-amino-1,3-dithianes via chiral N-phosphonyl imine-based Umpolung reaction without using chromatography and recrystallization. The Journal of Organic Chemistry. 76: 2792-7. PMID 21405041 DOI: 10.1021/Jo200070D |
0.505 |
|
2011 |
Pindi S, Kaur P, Shakya G, Li G. N-phosphinyl imine chemistry (I): design and synthesis of novel N-phosphinyl imines and their application to asymmetric aza-Henry reaction. Chemical Biology & Drug Design. 77: 20-9. PMID 21134217 DOI: 10.1111/J.1747-0285.2010.01047.X |
0.448 |
|
2011 |
Han J, Pan Y, Ji X, Mei H, Qian Y, Li G. Potassium Carbonate Catalyzed Regioselective Aminohalogenation of β-Nitrostyrenes by Using Benzyl Carbamate/N-Chlorosuccinimide as a New Nitrogen/Chlorine Source Synthesis. 2011: 3680-3686. DOI: 10.1055/S-0030-1260245 |
0.424 |
|
2011 |
Mei H, Han J, Li G, Pan Y. KOH-catalyzed highly efficient aminohalogenation of β-nitrostyrenes with t-butyl N,N-dichlorocarbamate as nitrogen/halogen source Rsc Advances. 1: 429. DOI: 10.1039/C1Ra00174D |
0.348 |
|
2011 |
Cheng C, Jiang B, Tu S, Li G. [4+2+1] Domino cyclization in water for chemo- and regioselective synthesis of spiro-substituted benzo[b]furo[3,4-e][1,4]diazepine derivatives Green Chemistry. 13: 2107-2115. DOI: 10.1039/C1Gc15183E |
0.454 |
|
2011 |
Kaur P, Wever W, Pindi S, Milles R, Gu P, Shi M, Li G. The GAP chemistry for chiral N-phosphonyl imine-based Strecker reaction Green Chemistry. 13: 1288-1292. DOI: 10.1039/C1Gc15029D |
0.501 |
|
2011 |
Kaur P, Wever W, Pindi S, Milles R, Gu P, Shi M, Li G. ChemInform Abstract: The GAP Chemistry for Chiral N-Phosphonyl Imine-Based Strecker Reaction. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201137182 |
0.345 |
|
2011 |
Jiang B, Rajale T, Wever W, Tu S, Li G. ChemInform Abstract: Multicomponent Reactions for the Synthesis of Heterocycles. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201107235 |
0.335 |
|
2010 |
Jiang B, Rajale T, Wever W, Tu SJ, Li G. Multicomponent reactions for the synthesis of heterocycles. Chemistry, An Asian Journal. 5: 2318-35. PMID 20922748 DOI: 10.1002/Asia.201000310 |
0.412 |
|
2010 |
Kaur P, Wever W, Rajale T, Li G. Asymmetric hydrophosphylation of chiral N-phosphonyl imines provides an efficient approach to chiral α-amino phosphonates. Chemical Biology & Drug Design. 76: 314-9. PMID 20887612 DOI: 10.1111/J.1747-0285.2010.01013.X |
0.445 |
|
2010 |
Mei H, Yan L, Han J, Li G, Pan Y. One-pot highly stereoselective synthesis of cyano aziridines via the CuCl-catalyzed aminochlorination of α,β-unsaturated nitriles and intramolecular S(N) 2 substitution. Chemical Biology & Drug Design. 76: 392-6. PMID 20880018 DOI: 10.1111/J.1747-0285.2010.01023.X |
0.488 |
|
2010 |
Sun H, Zhang G, Zhi S, Han J, Li G, Pan Y. Copper-catalyzed aminobromination/elimination process: an efficient access to alpha,beta-unsaturated vicinal haloamino ketones and esters. Organic & Biomolecular Chemistry. 8: 4236-9. PMID 20714671 DOI: 10.1039/C0Ob00283F |
0.307 |
|
2010 |
Kaur P, Pindi S, Wever W, Rajale T, Li G. Asymmetric catalytic N-phosphonyl imine chemistry: the use of primary free amino acids and Et2AlCN for asymmetric catalytic Strecker reaction. The Journal of Organic Chemistry. 75: 5144-50. PMID 20597482 DOI: 10.1021/Jo100865Q |
0.479 |
|
2010 |
Kaur P, Pindi S, Wever W, Rajale T, Li G. Asymmetric catalytic Strecker reaction of N-phosphonyl imines with Et2AlCN using amino alcohols and BINOLs as catalysts. Chemical Communications (Cambridge, England). 46: 4330-2. PMID 20464009 DOI: 10.1039/C0Cc00287A |
0.404 |
|
2010 |
Jiang B, Li C, Shi F, Tu SJ, Kaur P, Wever W, Li G. Four-component domino reaction providing an easy access to multifunctionalized tricyclo[6.2.2.0(1,6)]dodecane derivatives. The Journal of Organic Chemistry. 75: 2962-5. PMID 20356095 DOI: 10.1021/Jo1002278 |
0.407 |
|
2010 |
Sun H, Zhi SJ, Han JL, Li G, Pan Y. Highly regio- and stereoselective synthesis of alpha-(N-alkyl-N-p-toluenesulfonyl)-beta-bromo-ketones via Ni(OAc)2-catalyzed aminobromination of chalcones. Chemical Biology & Drug Design. 75: 269-76. PMID 20331646 DOI: 10.1111/J.1747-0285.2010.00938.X |
0.409 |
|
2010 |
Kaur P, Shakya G, Sun H, Pan Y, Li G. Chiral N-phosphonyl imine chemistry: an efficient asymmetric synthesis of chiral N-phosphonyl propargylamines. Organic & Biomolecular Chemistry. 8: 1091-6. PMID 20165799 DOI: 10.1039/B923914F |
0.466 |
|
2010 |
Li W, Yuan W, Pindi S, Shi M, Li G. Au/Ag-catalyzed intramolecular ring-opening of vinylidene-cyclopropanes (VDCPs): an easy access to functional tetrahydropyrans. Organic Letters. 12: 920-3. PMID 20141165 DOI: 10.1021/Ol902832S |
0.36 |
|
2010 |
Zhi SJ, Sun H, Zhang G, Li G, Pan Y. New catalytic system for aminohalogenation of beta-methyl-beta-nitrostyrenes to give opposite regiochemistry. Organic & Biomolecular Chemistry. 8: 628-31. PMID 20090980 DOI: 10.1039/B914944A |
0.385 |
|
2010 |
Li W, Yuan W, Shi M, Hernandez E, Li G. Rhodium(I)-catalyzed intramolecular ene reaction of vinylidenecyclopropanes and alkenes for the formation of bicyclo[5.1.0]octylenes. Organic Letters. 12: 64-7. PMID 19950891 DOI: 10.1021/Ol902505P |
0.44 |
|
2010 |
Ma N, Jiang B, Zhang G, Tu S, Wever W, Li G. New multicomponent domino reactions (MDRs) in water: highly chemo-, regio- and stereoselective synthesis of spiro{[1,3]dioxanopyridine}-4,6-diones and pyrazolo[3,4-b]pyridines Green Chemistry. 12: 1357-1361. DOI: 10.1039/C0Gc00073F |
0.448 |
|
2010 |
Sun H, Rajale T, Pan Y, Li G. Chiral N-phosphoryl imines: Design, synthesis and direct asymmetric addition reactions with diketones and diesters Tetrahedron Letters. 51: 4403-4407. DOI: 10.1016/J.Tetlet.2010.06.072 |
0.463 |
|
2010 |
Zhi S, An G, Sun H, Han J, Li G, Pan Y. The combination of TsNBr2/TsNH2 as the nitrogen/halo source for the aminobromination of β-methyl-β-nitrostyrenes catalyzed by Mn(OAc)2 Tetrahedron Letters. 51: 2745-2747. DOI: 10.1016/J.Tetlet.2010.03.060 |
0.696 |
|
2010 |
Zhang G, An G, Zheng J, Pan Y, Li G. Catalyst-free aminobromination of alkenes with N-methyl-p-toluenesulfonamide as nitrogen resource Tetrahedron Letters. 51: 987-989. DOI: 10.1016/J.Tetlet.2009.12.059 |
0.705 |
|
2010 |
Wu H, Ji X, Sun H, An G, Han J, Li G, Pan Y. Organocatalyzed regio- and stereoselective diamination of functionalized alkenes Tetrahedron. 66: 4555-4559. DOI: 10.1016/J.Tet.2010.04.054 |
0.749 |
|
2010 |
Zhi S, Mei H, Zhang G, Sun H, Han J, Li G, Pan Y. The combination of benzamides/NCS as nitrogen/halogen sources for aminohalogenation of β-nitrostyrenes resulting in dichlorinated haloamides Science China Chemistry. 53: 1946-1952. DOI: 10.1007/S11426-010-4001-4 |
0.43 |
|
2010 |
Zhi S, Sun H, Lin C, Zhang G, Li G, Pan Y. Regioselective aminohalogenation of β-nitrostyrenes using NCS and NBS as nitrogen/halogen sources Science China Chemistry. 53: 140-146. DOI: 10.1007/S11426-010-0028-9 |
0.42 |
|
2010 |
Ai T, Pindi S, Kattamuri PV, Li G. Chiral N -phosphonyl imine chemistry: asymmetric additions of glycine enolate to diphenyl diamine-based phosphonyl imines Science China-Chemistry. 53: 125-129. DOI: 10.1007/S11426-010-0026-Y |
0.505 |
|
2010 |
Kaur P, Pindi S, Wever W, Rajale T, Li G. ChemInform Abstract: Asymmetric Catalytic N-Phosphonyl Imine Chemistry: The Use of Primary Free Amino Acids and Et2AlCN for Asymmetric Catalytic Strecker Reaction. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201049063 |
0.303 |
|
2010 |
Sun H, Rajale T, Pan Y, Li G. ChemInform Abstract: Chiral N-Phosphoryl Imines: Design, Synthesis and Direct Asymmetric Addition Reactions with Diketones and Diesters. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201048174 |
0.354 |
|
2010 |
Kaur P, Shakya G, Sun H, Pan Y, Li G. ChemInform Abstract: Chiral N-Phosphonyl Imine Chemistry: An Efficient Asymmetric Synthesis of Chiral N-Phosphonyl Propargylamines. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201027173 |
0.332 |
|
2009 |
Jiang B, Wang X, Shi F, Tu SJ, Ai T, Ballew A, Li G. Microwave enabled umpulong mechanism based rapid and efficient four- and six-component domino formations of 2-(2'-azaaryl)imidazoles and anti-1,2-diarylethylbenzamides. The Journal of Organic Chemistry. 74: 9486-9. PMID 19938854 DOI: 10.1021/Jo902204S |
0.428 |
|
2009 |
Jiang B, Tu SJ, Kaur P, Wever W, Li G. Four-component domino reaction leading to multifunctionalized quinazolines. Journal of the American Chemical Society. 131: 11660-1. PMID 19722590 DOI: 10.1021/Ja904011S |
0.405 |
|
2009 |
Ai T, Li G. Chiral N-phosphonyl imine chemistry: asymmetric synthesis of alpha,beta-diamino esters by reacting phosphonyl imines with glycine enolates. Bioorganic & Medicinal Chemistry Letters. 19: 3967-9. PMID 19297153 DOI: 10.1016/J.Bmcl.2009.03.001 |
0.422 |
|
2009 |
Ai T, Han J, Chen ZX, Li G. Chiral N-phosphonyl imine chemistry: asymmetric synthesis of alpha-alkyl beta-amino ketones by reacting phosphonyl imines with ketone-derived enolates. Chemical Biology & Drug Design. 73: 203-8. PMID 19207422 DOI: 10.1111/J.1747-0285.2008.00771.X |
0.432 |
|
2009 |
Chen ZX, Ai T, Kaur P, Li G. Chiral N-phosphonyl imine chemistry: asymmetric additions of malonate-derived enolates to chiral N-phosphonyl imines for the synthesis of β-aminomalonates Tetrahedron Letters. 50: 1079-1081. DOI: 10.1016/J.Tetlet.2008.12.093 |
0.481 |
|
2009 |
Kaur P, Nguyen T, Li G. Chiral N‐Phosphonylimine Chemistry: Asymmetric Synthesis of N‐Phosphonyl β‐Amino Weinreb Amides European Journal of Organic Chemistry. 2009: 912-916. DOI: 10.1002/Ejoc.200801061 |
0.443 |
|
2008 |
Han J, Ai T, Nguyen T, Li G. Chiral N-phosphonyl imine chemistry: asymmetric additions of ester enolates for the synthesis of beta-amino acids. Chemical Biology & Drug Design. 72: 120-6. PMID 18631372 DOI: 10.1111/J.1747-0285.2008.00682.X |
0.42 |
|
2008 |
Kattuboina A, Kaur P, Ai T, Li G. Chiral N-phosphonyl imine chemistry: asymmetric aza-Henry reaction. Chemical Biology & Drug Design. 71: 216-23. PMID 18251775 DOI: 10.1111/J.1747-0285.2008.00633.X |
0.477 |
|
2008 |
Han J, Li T, Pan Y, Kattuboina A, Li G. Catalytic diamination of alkenes using N,N-dibromo-p-toluenesulfonamide as electrophile and nitriles as nucleophiles. Chemical Biology & Drug Design. 71: 71-7. PMID 18069987 DOI: 10.1111/J.1747-0285.2007.00604.X |
0.45 |
|
2008 |
Zhi S, Han J, Lin C, An G, Pan Y, Li G. Catalytic Aminohalogenation Reaction of β-Nitrostyrenes with N,N-Dichloro-p-toluenesulfonamide Resulting in Dichlorinated Haloamides with Opposite Regiochemistry to Previous Systems Synthesis. 2008: 1570-1574. DOI: 10.1055/S-2008-1072567 |
0.727 |
|
2008 |
Han J, Ai T, Li G. Chiral N-PhosphonylImine Chemistry: Asymmetric Addition of Ketone-DerivedEnolates for the Synthesis of β-Amino Ketones Synthesis. 2008: 2519-2526. DOI: 10.1055/S-2008-1067189 |
0.527 |
|
2008 |
Kattuboina A, Kaur P, Nguyen T, Li G. Chiral N-phosphonyl imine chemistry: asymmetric 1,2-additions of allylmagnesium bromides Tetrahedron Letters. 49: 3722-3724. DOI: 10.1016/J.Tetlet.2008.04.038 |
0.478 |
|
2008 |
Kattuboina A, Li G. Chiral N-phosphonyl imine chemistry: new reagents and their applications for asymmetric reactions Tetrahedron Letters. 49: 1573-1577. DOI: 10.1016/J.Tetlet.2008.01.028 |
0.488 |
|
2008 |
Qi MJ, Ai T, Shi M, Li G. Asymmetric catalytic aza-Morita–Baylis–Hillman reaction using chiral bifunctional phosphine amides as catalysts Tetrahedron. 64: 1181-1186. DOI: 10.1016/J.Tet.2007.11.039 |
0.488 |
|
2008 |
Kattuboina A, Kaur P, Nguyen T, Li G. ChemInform Abstract: Chiral N-Phosphonyl Imine Chemistry: Asymmetric 1,2-Additions of Allylmagnesium Bromides. Cheminform. 39. DOI: 10.1002/chin.200838063 |
0.329 |
|
2007 |
Tu S, Li C, Li G, Cao L, Shao Q, Zhou D, Jiang B, Zhou J, Xia M. Microwave-assisted combinatorial synthesis of polysubstituent imidazo[1,2-a]quinoline, pyrimido[1,2-a]quinoline and quinolino[1,2-a]quinazoline derivatives. Journal of Combinatorial Chemistry. 9: 1144-8. PMID 17953448 DOI: 10.1021/Cc700124G |
0.449 |
|
2007 |
Han J-, Zhi S-, Wang L-, Pan Y, Li G. Copper-Catalyzed Regio- and Stereoselective Aminochlorinations Synfacts. 2007: 507-507. DOI: 10.1055/S-2007-968444 |
0.339 |
|
2007 |
Wang YN, Kattuboina A, Ai T, Banerjee D, Li G. Chelation-controlled asymmetric aminohalogenation reaction Tetrahedron Letters. 48: 7894-7898. DOI: 10.1016/J.Tetlet.2007.08.099 |
0.453 |
|
2007 |
Li G, Kotti SRSS, Timmons C. Recent Development of Regio- and Stereoselective Aminohalogenation Reaction of Alkenes European Journal of Organic Chemistry. 2007: 2745-2758. DOI: 10.1002/Ejoc.200600990 |
0.428 |
|
2007 |
Han J, Zhi S, Wang L, Pan Y, Li G. CuCl-Catalyzed Regio- and Stereoselective Aminohalogenation of α,β-Unsaturated Nitriles European Journal of Organic Chemistry. 2007: 1332-1337. DOI: 10.1002/Ejoc.200600902 |
0.452 |
|
2007 |
Wang YN, Ni B, Headley AD, Li G. Ionic liquid, 1-n-butyl-3-methylimidazolium bis(trifluoro-methanesulfonyl) imide, resulted in the first catalyst-free aminohalogenation of electron-deficient alkenes Advanced Synthesis and Catalysis. 349: 319-322. DOI: 10.1002/CHIN.200722081 |
0.441 |
|
2006 |
Kattuboina A, Kaur P, Timmons C, Li G. Novel approach to multifunctionalized homoallylic alcohols via regioselective ring opening of aryl oxiranes with 3-iodo allenoates. Organic Letters. 8: 2771-4. PMID 16774253 DOI: 10.1021/Ol060828B |
0.372 |
|
2006 |
Saibabu Kotti SR, Timmons C, Li G. Vicinal diamino functionalities as privileged structural elements in biologically active compounds and exploitation of their synthetic chemistry. Chemical Biology & Drug Design. 67: 101-14. PMID 16492158 DOI: 10.1111/J.1747-0285.2006.00347.X |
0.32 |
|
2006 |
Li Q, Shi M, Timmons C, Li G. FeCl3-Catalyzed aminohalogenation of arylmethylenecyclopropanes and arylvinylidenecyclopropanes and corresponding mechanistic studies. Organic Letters. 8: 625-8. PMID 16468727 DOI: 10.1021/Ol052806F |
0.399 |
|
2006 |
Li Q, Shi M, Lyte JM, Li G. ZrCl4-catalyzed X–C/C–C bond formation for the geometric selective synthesis of (E)-β-iodo aza Morita–Baylis–Hillman (MBH) adducts Tetrahedron Letters. 47: 7699-7702. DOI: 10.1016/J.Tetlet.2006.08.128 |
0.415 |
|
2006 |
Han J, Li Y, Zhi S, Pan Y, Timmons C, Li G. Palladium-catalyzed aziridination of alkenes using N,N-dichloro-p-toluenesulfonamide as nitrogen source Tetrahedron Letters. 47: 7225-7228. DOI: 10.1016/J.Tetlet.2006.07.143 |
0.442 |
|
2006 |
Timmons C, Kattuboina A, Banerjee S, Li G. Highly Z/E stereoselective approach to β-iodo aza Morita–Baylis–Hillman adducts Tetrahedron. 62: 7151-7154. DOI: 10.1016/J.Tet.2006.01.114 |
0.412 |
|
2006 |
Liu J, Wang Y, Li G. Regio- and stereoselective synthesis of anti-1,3-diaryl-3-chloro-2-(o-nitrophenylsulfonylamino)-3-propan-1-ones through catalytic aminohalogenation reaction of α,β-unsaturated ketones European Journal of Organic Chemistry. 2006: 3112-3115. DOI: 10.1002/CHIN.200647103 |
0.479 |
|
2005 |
Ni B, Headley AD, Li G. Design and synthesis of C-2 substituted chiral imidazolium ionic liquids from amino acid derivatives. The Journal of Organic Chemistry. 70: 10600-2. PMID 16323882 DOI: 10.1021/Jo051888I |
0.449 |
|
2005 |
Timmons C, Mcpherson LM, Chen D, Wei H-, Li G. Manganese (IV) oxide-catalyzed electrophilic diamination of electron-deficient alkenes provides an easy synthesis of α,β-diamino acid and ketone derivatives for peptidomimetic studies* Journal of Peptide Research. 66: 249-254. PMID 16218992 DOI: 10.1111/J.1399-3011.2005.00294.X |
0.458 |
|
2005 |
Timmons C, Guo L, Liu J, Cannon JF, Li G. Asymmetric halo-Mannich-type reaction provides access to pyrrolidines and beta-proline derivatives. The Journal of Organic Chemistry. 70: 7634-9. PMID 16149793 DOI: 10.1021/Jo0509051 |
0.454 |
|
2005 |
Chen D, Guo L, Liu J, Kirtane S, Cannon JF, Li G. Functionalization of alpha,beta-unsaturated esters and ketones: a facile and highly stereoselective one-pot approach to N-protected alpha,beta-dehydroamino acid derivatives. Organic Letters. 7: 921-4. PMID 15727475 DOI: 10.1021/Ol050002U |
0.347 |
|
2005 |
Timmons C, Li G. The enantioselective halo aldol reaction utilizing cyclopropyl ketone-derived enolates Tetrahedron Letters. 46: 6949-6952. DOI: 10.1016/J.Tetlet.2005.07.163 |
0.468 |
|
2005 |
Chen D, Guo L, Kotti SRSS, Li G. The first asymmetric catalytic halo aldol reaction of β-iodo allenoates with aldehydes by using chiral salen catalyst Tetrahedron-Asymmetry. 16: 1757-1762. DOI: 10.1016/J.Tetasy.2005.03.038 |
0.47 |
|
2005 |
Timmons C, Kattuboina A, McPherson L, Mills J, Li G. Aza Diels–Alder reactions utilizing 4-iodo-2-trimethylsilyloxy-butadiene Tetrahedron. 61: 11837-11842. DOI: 10.1016/J.Tet.2005.10.018 |
0.477 |
|
2005 |
Xu X, Liu J, Chen D, Timmons C, Li G. A Lewis Acid Promoted Asymmetric Umpolung Reaction with ChiralN‐Sulfinyl Imines as the Electrophiles European Journal of Organic Chemistry. 2005: 1805-1809. DOI: 10.1002/Ejoc.200400775 |
0.503 |
|
2005 |
Chen D, Guo L, Kotti SRSS, Li G. The First Asymmetric Catalytic Halo Aldol Reaction of β-Iodo Allenoates with Aldehydes by Using Chiral Salen Catalyst. Cheminform. 36. DOI: 10.1002/CHIN.200540034 |
0.321 |
|
2005 |
Xu X, Liu J, Chen D, Timmons C, Li G. A Lewis Acid Promoted Asymmetric Umpolung Reaction with Chiral N-Sulfinyl Imines as the Electrophiles. Cheminform. 36. DOI: 10.1002/CHIN.200535034 |
0.339 |
|
2004 |
Xu X, Kotti SR, Liu J, Cannon JF, Headley AD, Li G. Ionic liquid media resulted in the first asymmetric aminohalogenation reaction of alkenes. Organic Letters. 6: 4881-4. PMID 15606090 DOI: 10.1021/Ol048045I |
0.457 |
|
2004 |
Wei HX, Timmons C, Farag MA, Pare PW, Li G. MgI2-catalyzed halo aldol reaction: a practical approach to (E)-beta-iodovinyl-beta'-hydroxyketones. Organic & Biomolecular Chemistry. 2: 2893-6. PMID 15480451 DOI: 10.1039/B409056J |
0.334 |
|
2004 |
Timmons C, Chen D, Cannon JF, Headley AD, Li G. New asymmetric halo aldol reaction provides a novel approach to biologically important chiral cyclothers and cycloamines. Organic Letters. 6: 2075-8. PMID 15176822 DOI: 10.1021/Ol049255Y |
0.502 |
|
2004 |
Li G, Chen D, Timmons C, Guo L, Xu X. One-Pot Stereoselective Synthesis ofanti3-Alkyl and 3-Aryl-N-p-tosyl-aziridine-2-ketones and 3-Aryl-N-p-tosyl-aziridine-2-carboxylates Synthesis. 2004: 2479-2484. DOI: 10.1055/S-2004-831203 |
0.451 |
|
2004 |
Kotti SRSS, Xu X, Wang Y, Headley AD, Li G. Ionic liquid media resulted in more efficient regio- and stereoselective aminohalogenation of cinnamic esters Tetrahedron Letters. 45: 7209-7212. DOI: 10.1016/J.Tetlet.2004.08.040 |
0.419 |
|
2004 |
Kotti SRSS, Xu X, Li G, Headley AD. Efficient nucleophilic substitution reactions of highly functionalized allyl halides in ionic liquid media Tetrahedron Letters. 45: 1427-1431. DOI: 10.1016/J.Tetlet.2003.12.051 |
0.441 |
|
2004 |
Timmons C, Chen D, Barney CE, Kirtane S, Li G. The combination of 2-NsNH2/NCS and MeCN as the nitrogen sources for the regio- and stereoselective formation of imidazolines from α,β-unsaturated ketones Tetrahedron. 60: 12095-12099. DOI: 10.1016/J.Tet.2004.10.022 |
0.426 |
|
2004 |
Wei H, Jasoni RL, Hu J, Li G, Paré PW. Z/E stereoselective synthesis of β-bromo baylis-hillman ketones using MgBr2 as promoter via a one-pot three-component reaction Tetrahedron. 60: 10233-10237. DOI: 10.1016/J.Tet.2004.08.097 |
0.403 |
|
2004 |
Wei H, Hu J, Jasoni RL, Li G, Paré PW. Synthesis of Substituted α‐(Hydroxymethyl)‐β‐iodoacrylates via MgI2‐Promoted Stereoselective Aldol Coupling Helvetica Chimica Acta. 87: 2359-2363. DOI: 10.1002/Hlca.200490212 |
0.491 |
|
2004 |
Chen D, Timmons C, Liu J, Headley A, Li G. The first enantioselective halo aldol reaction of ethyl propiolate and aldehydes European Journal of Organic Chemistry. 3330-3335. DOI: 10.1002/Ejoc.200400230 |
0.484 |
|
2004 |
Flowers RA, Xu X, Timmons C, Li G. A polymer-supported phosphoramide as a Lewis-base catalyst for the catalytic aldol reaction European Journal of Organic Chemistry. 2988-2990. DOI: 10.1002/Ejoc.200400228 |
0.411 |
|
2004 |
Chen D, Timmons C, Chao S, Li G. Regio- and Stereoselective Copper-Catalyzed Synthesis of Vicinal Haloamino Ketones from α,β-Unsaturated Ketones European Journal of Organic Chemistry. 2004: 3097-3101. DOI: 10.1002/Ejoc.200400050 |
0.463 |
|
2003 |
Karur S, Kotti SRSS, Xu X, Cannon JF, Headley A, Li G. A Catalytic Reaction of Alkynes via Multiple-Site Functionalization Journal of the American Chemical Society. 125: 13340-13341. PMID 14583013 DOI: 10.1021/Ja0304188 |
0.442 |
|
2003 |
Pei W, Wei HX, Chen D, Headley AD, Li G. N,N-Dichloro-2-nitrobenzenesulfonamide as the Electrophilic Nitrogen Source for Direct Diamination of Enones Journal of Organic Chemistry. 68: 8404-8408. PMID 14575464 DOI: 10.1021/Jo030193J |
0.416 |
|
2003 |
Pei W, Timmons C, Xu X, Wei HX, Li G. Novel imidazolination reaction of alkenes provides an easy access to new alpha,beta-differentiated 1,2-vicinal diamines. Organic & Biomolecular Chemistry. 1: 2919-21. PMID 12968342 DOI: 10.1039/B305149H |
0.354 |
|
2003 |
Chen D, Timmons C, Wei H, Li G. Direct electrophilic diamination of functionalized alkenes without the use of any metal catalysts. Journal of Organic Chemistry. 68: 5742-5745. PMID 12839474 DOI: 10.1021/Jo030098A |
0.406 |
|
2003 |
Li G, Xu X, Chen D, Timmons C, Carducci MD, Headley AD. Asymmetric halo aldol reaction (AHA) Organic Letters. 5: 329-331. PMID 12556184 DOI: 10.1021/Ol027344+ |
0.444 |
|
2003 |
Xu X, Chen D, Wei HX, Li G, Xiao TL, Armstrong DW. First asymmetric synthesis of chiral beta-iodo Baylis-Hillman esters via tandem 1,4-conjugate addition/carbonyl coupling reactions. Chirality. 15: 139-42. PMID 12520505 DOI: 10.1002/Chir.10179 |
0.43 |
|
2003 |
Wei HX, Kim SH, Li G. Electrophilic diamination of alkenes by using FeCl(3)-PPh(3) complex as the catalyst. The Journal of Organic Chemistry. 67: 4777-81. PMID 12098288 DOI: 10.1021/Jo0200769 |
0.458 |
|
2003 |
Chen D, Kim SH, Hodges B, Li G. The cinnamate-based aminohalogenation provides an easy access to anti methyl 3-aryl-N-p-tosyl- and N-o-nosyl-aziridine-2-carboxylates Arkivoc. 2003. DOI: 10.3998/Ark.5550190.0004.C07 |
0.381 |
|
2003 |
Wei H, Chen D, Xu X, Li G, Paré PW. Asymmetric synthesis of chiral β-iodo Baylis–Hillman esters using MgI2 as promoter via a one-pot three-component reaction Tetrahedron-Asymmetry. 14: 971-974. DOI: 10.1016/S0957-4166(03)00115-0 |
0.415 |
|
2003 |
Karur S, Hardin J, Headley A, Li G. A novel approach to Morita-Baylis-Hillman (MBH) lactones via the Lewis acid-promoted couplings of α,β-unsaturated lactone with aldehydes Tetrahedron Letters. 44: 2991-2994. DOI: 10.1016/S0040-4039(03)00380-0 |
0.397 |
|
2003 |
Timmons C, Chen D, Xu X, Li G. The Combination of TsNH2 and NCS as Nitrogen and Chlorine Sources for Direct Diamination of Enones European Journal of Organic Chemistry. 2003: 3850-3854. DOI: 10.1002/Ejoc.200300326 |
0.43 |
|
2003 |
Wei H, Chen D, Xu X, Li G, Pare PW. Asymmetric Synthesis of Chiral β-Iodo Baylis—Hillman Esters Using MgI2 as Promoter via a One-Pot Three-Component Reaction. Cheminform. 34. DOI: 10.1002/CHIN.200332040 |
0.364 |
|
2002 |
Pei W, Wei HX, Li G. The Baylis-Hillman condensation of alpha,beta-conjugate cycloketones with aldehydes using diethylaluminum iodide alone as the promoter. Chemical Communications (Cambridge, England). 2412-3. PMID 12430466 DOI: 10.1039/B206736F |
0.324 |
|
2002 |
Wei HX, Kim SH, Li G. A new halo aldol reaction: three-component reaction via 1,4-robust activation of ethynyl alkyl ketones for stereoselective formations of versatile aldol adducts. Organic Letters. 4: 3691-3. PMID 12375920 DOI: 10.1021/Ol020146Y |
0.402 |
|
2002 |
Pei W, Wei HX, Li G. Lewis acid-promoted Baylis-Hillman-type reaction of alpha,beta-unsaturated ethyl thioester with aldehydes without the use of a Lewis base. Chemical Communications (Cambridge, England). 1856-7. PMID 12271643 DOI: 10.1039/B204210J |
0.309 |
|
2002 |
Kim S, Wei H, Gao J, Li G. Three-Component Halo Aldol Condensation of Thioacrylates with Aldehydes Mediated by Titanium (IV) Halide Molecules. 7: 89-95. DOI: 10.3390/70100089 |
0.416 |
|
2002 |
Li G, Wei H, Gao JJ, Johnson J. Z/E STEREOSELECTIVE SYNTHESIS OF β-BROMO BAYLIS-HILLMAN KETONES VIA A ONE-POT THREE-COMPONENT X–C/C–C FORMATION REACTION Synthetic Communications. 32: 1765-1773. DOI: 10.1081/Scc-120004273 |
0.433 |
|
2002 |
Wei H, Li G, Gao JJ, Paré PW. Synthesis of β-iodo-α-(hydroxyalkyl)acrylates: a convenient and stereoselective reaction Tetrahedron Letters. 43: 5677-5680. DOI: 10.1016/S0040-4039(02)01106-1 |
0.423 |
|
2002 |
Wei H, Siruta S, Li G. New catalytic diamination of alkenes provides a novel access to 1-p-toluenesulfonyl-3-trichloromethyl-4,5-imidazolines Tetrahedron Letters. 43: 3809-3812. DOI: 10.1016/S0040-4039(02)00694-9 |
0.445 |
|
2001 |
Li G, Wei HX, Kim SH, Carducci MD. A Novel Electrophilic Diamination Reaction of Alkenes. Angewandte Chemie (International Ed. in English). 40: 4277-4280. PMID 29712117 DOI: 10.1002/1521-3773(20011119)40:22<4277::Aid-Anie4277>3.0.Co;2-I |
0.45 |
|
2001 |
Li G, Wei HX, Phelps BS, Purkiss DW, Kim SH. The asymmetric catalytic aldol reaction of allenolates with aldehydes using n-fluoroacyl oxazaborolidine as the catalyst. Organic Letters. 3: 823-6. PMID 11263891 DOI: 10.1021/Ol000377+ |
0.422 |
|
2001 |
Wei H, Gao JJ, Li G. Substoichiometric TiCl4-mediated vicinal difunctionalization of α,β-acetylenic ketones for the synthesis of β-halo Baylis–Hillman olefins Tetrahedron Letters. 42: 9119-9122. DOI: 10.1016/S0040-4039(01)02020-2 |
0.358 |
|
2001 |
Li G, Wei H, Kim SH. Unexpected copper-catalyzed aminohalogenation reaction of olefins using N-halo-N-metallo-sulfonamide as the nitrogen and halogen sources Tetrahedron. 57: 8407-8411. DOI: 10.1016/S0040-4020(01)00847-X |
0.434 |
|
2001 |
Wei H, Kim SH, Li G. The first transition metal–ligand complex-catalyzed regioselective and stereoselective aminohalogenation of cinnamic esters Tetrahedron. 57: 3869-3873. DOI: 10.1016/S0040-4020(01)00228-9 |
0.44 |
|
2000 |
Li G, Wei HX, Kim SH. Copper-catalyzed aminohalogenation using the 2-NsNCl(2)/2-NsNHNa combination as the nitrogen and halogen sources for the synthesis of anti-alkyl 3-chloro-2-(o-nitrobenzenesulfonamido)-3-arylpropionates. Organic Letters. 2: 2249-52. PMID 10930255 DOI: 10.1021/Ol000120B |
0.423 |
|
2000 |
Li G, Gao J, Wei H, Enright M. New CC Bond Formation via Nonstoichiometric Titanium(IV) Halide Mediated Vicinal Difunctionalization of α,β-Unsaturated Acyclic Ketones Organic Letters. 2: 617-620. PMID 10814392 DOI: 10.1021/Ol9904040 |
0.447 |
|
2000 |
Wei H, Karur S, Li G. Halogeno Aldol Reaction of Ethyl Vinyl Ketone and Aldehydes Mediated by Titanium Tetrachloride Molecules. 5: 1408-1416. DOI: 10.3390/51201408 |
0.413 |
|
2000 |
Li G, Wei H, Gao JJ, Caputo TD. TiCl4-Mediated Baylis–Hillman and aldol reactions without the direct use of a Lewis base Tetrahedron Letters. 41: 1-5. DOI: 10.1016/S0040-4039(99)01992-9 |
0.378 |
|
2000 |
Li G, Hee Kim S, Wei H. α,β-Differentiated tandem diamination of cinnamic esters using N,N-dichloro-2-nitrobenzenesulfonamide and acetonitrile as the nitrogen sources Tetrahedron Letters. 41: 8699-8703. DOI: 10.1016/S0040-4039(00)01579-3 |
0.427 |
|
2000 |
Li G, Kim SH, Wei H. Highly Efficient Deprotection of N-p-Toluenesulfinyl Group of β-Branched Baylis–Hillman Adducts by Using Amberlite IR-120 (Plus) Ion-Exchange Resin Tetrahedron. 56: 719-723. DOI: 10.1016/S0040-4020(99)01064-9 |
0.347 |
|
2000 |
Wei H, Kim SH, Caputo TD, Purkiss DW, Li G. Highly Stereoselective α-Hydroxyalkylation/Chlorination of α,β-Acetylenic Ketones—An Efficient Approach to β-Halogeno Baylis–Hillman Adducts Tetrahedron. 56: 2397-2401. DOI: 10.1016/S0040-4020(00)00151-4 |
0.36 |
|
1999 |
Li G, Wei HX, Whittlesey BR, Batrice NN. Novel Asymmetric C-C Bond Formation Process Promoted by Et(2)AlCl and Its Application to the Stereoselective Synthesis of Unusual beta-Branched Baylis-Hillman Adducts. The Journal of Organic Chemistry. 64: 1061-1064. PMID 11674192 DOI: 10.1021/Jo981976L |
0.322 |
|
1999 |
Wei H, Willis S, Li G. Z/E Selective Synthesis of β,β-Disubstituted and (Z)-β-Monosubstituted Baylis-Hillman Adducts Via Anionic Additions of Vinylcuprates to Aldehydes Synthetic Communications. 29: 2959-2966. DOI: 10.1080/00397919908086469 |
0.33 |
|
1999 |
Kim SH, Wei H, Willis S, Li G. A Mild Procedure for the Stereospecific Transformation oftransCinnamic Acid Derivatives tocisβ-Bromostyrenes Synthetic Communications. 29: 4179-4185. DOI: 10.1080/00397919908085891 |
0.367 |
|
1999 |
Li G, Wei H, Kim aSH, Neighbors M. Transition Metal-Catalyzed Regioselective and Stereoselective Aminochlorination of Cinnamic Esters Organic Letters. 1: 395-398. DOI: 10.1021/Ol990059E |
0.457 |
|
1999 |
Wei H, Hook JD, Fitzgerald KA, Li G. Asymmetric synthesis of β-monosubstituted and β,β-disubstituted N-(p-toluenesulfinyl)-α-(aminoalkyl)acrylates via anionic additions of (α-carbalkoxyvinyl)cuprates to thiooxime S-oxides Tetrahedron-Asymmetry. 10: 661-665. DOI: 10.1016/S0957-4166(99)00036-1 |
0.35 |
|
1999 |
Li G, Wei H, Hook JD. Ytterbium(III) triflate-catalyzed asymmetric nucleophilic addition of functionalized lithium (α-carbalkoxyvinyl)cuprates to chiral p-toluenesulfinimines (thiooxime S-oxides) Tetrahedron Letters. 40: 4611-4614. DOI: 10.1016/S0040-4039(99)00756-X |
0.405 |
|
1998 |
Li G, Lenington R, Willis S, Kim SH. New synthesis of Evans chiral oxazolidinones by using Sharpless AA reaction Journal of the Chemical Society-Perkin Transactions 1. 1753-1754. DOI: 10.1039/A801404C |
0.457 |
|
1998 |
Wei H, Willis S, Li G. Lewis acid-promoted carbonyl addition of lithium (α-carbalkoxyvinyl)cuprates to aldehydes provides a novel asymmetric synthesis of β,β-disubstituted α-(hydroxyalkyl)acrylates Tetrahedron Letters. 39: 8203-8206. DOI: 10.1016/S0040-4039(98)01875-9 |
0.361 |
|
1998 |
Li G, Wei H, Willis S. A new stereospecific synthesis of unusual (Z)-β-branched Baylis-Hillman adducts Tetrahedron Letters. 39: 4607-4610. DOI: 10.1016/S0040-4039(98)00850-8 |
0.41 |
|
1996 |
Li G, Angert HH, Sharpless KB. N-Halocarbamate Salts Lead to More Efficient Catalytic Asymmetric Aminohydroxylation Angewandte Chemie International Edition in English. 35: 2813-2817. DOI: 10.1002/Anie.199628131 |
0.53 |
|
1996 |
Li G, Chang H, Sharpless KB. Catalytic Asymmetric Aminohydroxylation(AA) of Olefins Angewandte Chemie International Edition in English. 35: 451-454. DOI: 10.1002/Anie.199604511 |
0.541 |
|
1996 |
Li G, Angert HH, Sharpless KB. Erhöhung der Effizienz der katalytischen asymmetrischen Aminohydroxylierung durchN-Halogencarbamat-Salze Angewandte Chemie. 108: 2995-2999. DOI: 10.1002/Ange.19961082325 |
0.403 |
|
1996 |
Li G, Chang H, Sharpless KB. Katalytische asymmetrische Aminohydroxylierung (AA) von Olefinen Angewandte Chemie. 108: 449-452. DOI: 10.1002/Ange.19961080409 |
0.385 |
|
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