| Year |
Citation |
Score |
| 2023 |
Chen YH, Duan M, Lin SL, Liu YW, Cheng JK, Xiang SH, Yu P, Houk KN, Tan B. Organocatalytic aromatization-promoted umpolung reaction of imines. Nature Chemistry. PMID 38062248 DOI: 10.1038/s41557-023-01384-x |
0.399 |
|
| 2023 |
Lin SL, Chen YH, Liu HH, Xiang SH, Tan B. Enantioselective Synthesis of Chiral Cyclobutenes Enabled by Brønsted Acid-Catalyzed Isomerization of BCBs. Journal of the American Chemical Society. 145: 21152-21158. PMID 37732875 DOI: 10.1021/jacs.3c06525 |
0.4 |
|
| 2023 |
Jiang PY, Wu S, Wang GJ, Xiang SH, Tan B. Synthesis of Axially Chiral QUINAP Derivatives by Ketone-Catalyzed Enantioselective Oxidation. Angewandte Chemie (International Ed. in English). e202309272. PMID 37587093 DOI: 10.1002/anie.202309272 |
0.322 |
|
| 2023 |
Kee Cheng J, Tan B. Chiral Phosphoric Acid-Catalyzed Enantioselective Synthesis of Axially Chiral Compounds Involving Indole Derivatives. Chemical Record (New York, N.Y.). e202300147. PMID 37358342 DOI: 10.1002/tcr.202300147 |
0.448 |
|
| 2023 |
Da BC, Wang YB, Cheng JK, Xiang SH, Tan B. Organocatalytic Atroposelective Cross-Coupling of 1-Azonaphthalenes and 2-Naphthols. Angewandte Chemie (International Ed. in English). e202303128. PMID 37186009 DOI: 10.1002/anie.202303128 |
0.339 |
|
| 2023 |
Chen T, Tan B, Huang Z, Mao G, Chen S, Deng G. Brønsted Acid Promoted Facile Synthesis of Benzoacridines from Aromatic Aldehydes and N-phenyl Naphthylamines. Chemistry & Biodiversity. e202300122. PMID 36896824 DOI: 10.1002/cbdv.202300122 |
0.323 |
|
| 2023 |
Chen P, Lv MJ, Cheng JK, Xiang SH, Ren XZ, Zhang J, Tan B. Enantioselective construction of triaryl-substituted all-carbon quaternary stereocenters organocatalytic arylation of oxindoles with azonaphthalenes. Chemical Science. 14: 2330-2335. PMID 36873834 DOI: 10.1039/d2sc07103g |
0.441 |
|
| 2022 |
Cai B, Cui Y, Zhou J, Wang Y, Yang L, Tan B, Wang J. Asymmetric Hydrophosphinylation of Alkynes: Facile Access to Axially Chiral Styrene-Phosphines. Angewandte Chemie (International Ed. in English). PMID 36424372 DOI: 10.1002/anie.202215820 |
0.405 |
|
| 2022 |
He SJ, Zhu S, Qiu SQ, Ding WY, Cheng JK, Xiang SH, Tan B. Phosphoric Acid-Catalyzed Enantioselective Synthesis of Axially Chiral Anthrone-based Compounds. Angewandte Chemie (International Ed. in English). e202213914. PMID 36346195 DOI: 10.1002/anie.202213914 |
0.371 |
|
| 2022 |
Cheng JK, Xiang SH, Tan B. Organocatalytic Enantioselective Synthesis of Axially Chiral Molecules: Development of Strategies and Skeletons. Accounts of Chemical Research. PMID 36177502 DOI: 10.1021/acs.accounts.2c00509 |
0.426 |
|
| 2022 |
Ding WY, Zhao HW, Cheng JK, Lu Z, Xiang SH, Tan B. β-C-Glycosylation with 2-Oxindole Acceptors via Palladium-Catalyzed Decarboxylative Reactions. Organic Letters. 24: 7031-7036. PMID 36129413 DOI: 10.1021/acs.orglett.2c02881 |
0.332 |
|
| 2022 |
Qiu SQ, Chen Y, Peng XJ, He SJ, Cheng JK, Wang YB, Xiang SH, Song J, Yu P, Zhang JM, Tan B. Asymmetric Construction of Aryl-Alkene Axis by Palladium-Catalyzed Suzuki-Miyaura Coupling Reaction. Angewandte Chemie (International Ed. in English). PMID 36111538 DOI: 10.1002/anie.202211211 |
0.414 |
|
| 2022 |
Li HH, Li S, Cheng JK, Xiang SH, Tan B. Direct arylation of N-heterocycles enabled by photoredox catalysis. Chemical Communications (Cambridge, England). PMID 35297913 DOI: 10.1039/d2cc01212j |
0.304 |
|
| 2022 |
Xia W, Zhou ZA, Lv J, Xiang SH, Wang YB, Tan B. Facile synthesis of -aryl phenothiazines and phenoxazines Brønsted acid catalyzed C-H amination of arenes. Chemical Communications (Cambridge, England). PMID 35019918 DOI: 10.1039/d1cc06730c |
0.367 |
|
| 2021 |
Tan B, An QJ, Xia W, Ding WY, Liu HH, Xiang SH, Wang YB, Zhong G. Nitrosobenzene-Enabled Chiral Phosphoric Acid Catalyzed Enantioselective Construction of Atropisomeric N-Arylbenzimidazoles. Angewandte Chemie (International Ed. in English). PMID 34553823 DOI: 10.1002/anie.202111251 |
0.548 |
|
| 2021 |
Yang J, Zhang JW, Bao W, Qiu SQ, Li S, Xiang SH, Song J, Zhang J, Tan B. Chiral Phosphoric Acid-Catalyzed Remote Control of Axial Chirality at Boron-Carbon Bond. Journal of the American Chemical Society. PMID 34384026 DOI: 10.1021/jacs.1c05079 |
0.385 |
|
| 2021 |
Zhang JW, Xiang SH, Li S, Tan B. Copper-Catalyzed Synthesis of Axially Chiral Biaryls with Diaryliodonium Salts as Arylation Reagents. Molecules (Basel, Switzerland). 26. PMID 34072116 DOI: 10.3390/molecules26113223 |
0.411 |
|
| 2021 |
Jiang PY, Fan KF, Li S, Xiang SH, Tan B. Metal-free oxidative cross-coupling enabled practical synthesis of atropisomeric QUINOL and its derivatives. Nature Communications. 12: 2384. PMID 33888700 DOI: 10.1038/s41467-021-22621-2 |
0.333 |
|
| 2020 |
Tan B, Zhang L, Shen J, Wu S, Zhong G, Wang YB. Design and Atroposelective Construction of IAN analogues via Organocatalytic Asymmetric Heteroannulation of Alkynes. Angewandte Chemie (International Ed. in English). PMID 32886439 DOI: 10.1002/Anie.202010598 |
0.655 |
|
| 2020 |
Yan S, Xia W, Li S, Song Q, Xiang SH, Tan B. Correction to "Michael Reaction Inspired Atroposelective Construction of Axially Chiral Biaryls". Journal of the American Chemical Society. PMID 32452198 DOI: 10.1021/Jacs.0C05283 |
0.487 |
|
| 2020 |
Tan B, Chen YH, Li HH, Xiang XH, Li S, Zhang X. Organocatalytic Enantioselective Synthesis of Atropisomeric Aryl-p-quinones: Platform Molecules for Diversity-oriented Synthesis of Biaryldiols. Angewandte Chemie (International Ed. in English). PMID 32277551 DOI: 10.1002/Ange.202004671 |
0.46 |
|
| 2020 |
Yan S, Li S, Song Q, Tan B, Xia W, Xiang SH. Michael Reaction Inspired Atroposelective Construction of Axially Chiral Biaryls. Journal of the American Chemical Society. PMID 32267146 DOI: 10.1021/Jacs.0C01963 |
0.499 |
|
| 2020 |
Tan B, Xia W, An QJ, Xiang SH, Li S, Wang YB. Chiral-Phosphoric-Acid-Catalyzed Atroposelective C-H Amination of Arenes. Angewandte Chemie (International Ed. in English). PMID 32017378 DOI: 10.1002/Anie.202000585 |
0.442 |
|
| 2020 |
Ding W, Yu P, An Q, Bay KL, Xiang S, Li S, Chen Y, Houk KN, Tan B. DFT-Guided Phosphoric-Acid-Catalyzed Atroposelective Arene Functionalization of Nitrosonaphthalene Chem. 6: 2046-2059. DOI: 10.1016/J.Chempr.2020.06.001 |
0.516 |
|
| 2020 |
Zhang J, Wang Y, Sun H, Li S, Xiang S, Tan B. Enantioselective three-component Ugi reaction catalyzed by chiral phosphoric acid Science China-Chemistry. 63: 47-54. DOI: 10.1007/S11426-019-9606-2 |
0.534 |
|
| 2020 |
Zhang J, Qi L, Li S, Xiang S, Tan B. Direct Construction of NOBINs via Domino Arylation and Sigmatropic Rearrangement Reactions Chinese Journal of Chemistry. DOI: 10.1002/Cjoc.202000358 |
0.454 |
|
| 2020 |
Li S, Xiang S, Tan B. Chiral Phosphoric Acid Creates Promising Opportunities for Enantioselective Photoredox Catalysis Chinese Journal of Chemistry. 38: 213-214. DOI: 10.1002/Cjoc.201900472 |
0.413 |
|
| 2019 |
Zhu S, Chen YH, Wang YB, Yu P, Li SY, Xiang SH, Wang JQ, Xiao J, Tan B. Organocatalytic atroposelective construction of axially chiral arylquinones. Nature Communications. 10: 4268. PMID 31537811 DOI: 10.1038/S41467-019-12269-4 |
0.478 |
|
| 2019 |
Tan B, Wang YB, Wu QH, Zhou ZP, Xiang SH, Cui Y, Yu P. Asymmetric Construction of Axially Chiral 2-Arylpyrroles via Chirality Transfer of Atropisomeric Alkenes. Angewandte Chemie (International Ed. in English). PMID 31338946 DOI: 10.1002/Anie.201907470 |
0.515 |
|
| 2019 |
Lu DL, Chen YH, Xiang SH, Yu P, Tan B, Li S. Atroposelective Construction of Arylindoles by Chiral Phosphoric Acid-Catalyzed Cross-Coupling of Indoles and Quinones. Organic Letters. PMID 31334666 DOI: 10.1021/Acs.Orglett.9B02143 |
0.482 |
|
| 2019 |
Zhang L, Xiang SH, Wang JJ, Xiao J, Wang JQ, Tan B. Phosphoric acid-catalyzed atroposelective construction of axially chiral arylpyrroles. Nature Communications. 10: 566. PMID 30718716 DOI: 10.1038/S41467-019-08447-Z |
0.505 |
|
| 2019 |
Wang Y, Yu P, Zhou Z, Zhang J, Wang J(, Luo S, Gu Q, Houk KN, Tan B. Rational design, enantioselective synthesis and catalytic applications of axially chiral EBINOLs Nature Catalysis. 2: 504-513. DOI: 10.1038/s41929-019-0278-7 |
0.337 |
|
| 2019 |
Zhang L, Da B, Xiang S, Zhu S, Yuan Z, Guo Z, Tan B. Organocatalytic double arylation of 3-isothiocyanato oxindoles: Stereocontrolled synthesis of complex spirooxindoles Tetrahedron. 75: 1689-1696. DOI: 10.1016/J.Tet.2018.11.016 |
0.547 |
|
| 2018 |
Zhang LL, Zhang JW, Xiang SH, Guo Z, Tan B. Remote Control of Axial Chirality: Synthesis of Spirooxindole-Urazoles via Desymmetrization of ATAD. Organic Letters. PMID 30221944 DOI: 10.1021/Acs.Orglett.8B02361 |
0.504 |
|
| 2018 |
Zhang J, Yu P, Li SY, Sun H, Xiang SH, Wang JJ, Houk KN, Tan B. Asymmetric phosphoric acid-catalyzed four-component Ugi reaction. Science (New York, N.Y.). 361. PMID 30213886 DOI: 10.1126/Science.Aas8707 |
0.514 |
|
| 2018 |
Wang YB, Tan B. Construction of Axially Chiral Compounds via Asymmetric Organocatalysis. Accounts of Chemical Research. PMID 29419282 DOI: 10.1021/Acs.Accounts.7B00602 |
0.565 |
|
| 2018 |
Qi LW, Mao JH, Zhang J, Tan B. Organocatalytic asymmetric arylation of indoles enabled by azo groups. Nature Chemistry. 10: 58-64. PMID 29256504 DOI: 10.1038/Nchem.2866 |
0.502 |
|
| 2018 |
Zhang X, Chen Y, Tan B. Organocatalytic enantioselective transformations involving quinone derivatives as reaction partners Tetrahedron Letters. 59: 473-486. DOI: 10.1016/J.Tetlet.2017.12.055 |
0.441 |
|
| 2018 |
Zhang L, Zhang J, Xiang S, Guo Z, Tan B. Stereoselective Construction of Complex Spirooxindoles via Bisthiourea Catalyzed Three‐Component Reactions Chinese Journal of Chemistry. 36: 1182-1186. DOI: 10.1002/Cjoc.201800368 |
0.432 |
|
| 2017 |
Tan B, Chen YH, Qi LW, Fang F. Practical Approach to Axially Chiral Biaryl-amino-alcohols via Organocatalytic Atroposelective Arylation of 2-Naphthylamines. Angewandte Chemie (International Ed. in English). PMID 29105896 DOI: 10.1002/Anie.201710537 |
0.407 |
|
| 2017 |
Zheng SC, Wu S, Zhou Q, Chung LW, Ye L, Tan B. Erratum: Organocatalytic atroposelective synthesis of axially chiral styrenes. Nature Communications. 8: 16119. PMID 28653676 DOI: 10.1038/Ncomms16119 |
0.386 |
|
| 2017 |
Wang YB, Zheng SC, Hu YM, Tan B. Brønsted acid-catalysed enantioselective construction of axially chiral arylquinazolinones. Nature Communications. 8: 15489. PMID 28524863 DOI: 10.1038/Ncomms15489 |
0.504 |
|
| 2017 |
Zheng SC, Wu S, Zhou Q, Chung LW, Ye L, Tan B. Organocatalytic atroposelective synthesis of axially chiral styrenes. Nature Communications. 8: 15238. PMID 28466872 DOI: 10.1038/Ncomms15238 |
0.502 |
|
| 2017 |
Zhang L, Zhang J, Ma J, Cheng DJ, Tan B. Highly Atroposelective Synthesis of Arylpyrroles by Catalytic Asymmetric Paal-Knorr Reaction. Journal of the American Chemical Society. PMID 28106384 DOI: 10.1021/Jacs.6B09634 |
0.543 |
|
| 2016 |
Li L, Li ZL, Wang FL, Guo Z, Cheng YF, Wang N, Dong XW, Fang C, Liu J, Hou C, Tan B, Liu XY. Radical aryl migration enables diversity-oriented synthesis of structurally diverse medium/macro- or bridged-rings. Nature Communications. 7: 13852. PMID 28004746 DOI: 10.1038/Ncomms13852 |
0.374 |
|
| 2016 |
Li S, Zhang JW, Li XL, Cheng DJ, Tan B. Phosphoric Acid-Catalyzed Asymmetric Synthesis of SPINOL Derivatives. Journal of the American Chemical Society. PMID 27935306 DOI: 10.1021/Jacs.6B11435 |
0.526 |
|
| 2016 |
Xu JH, Zheng SC, Zhang JW, Liu XY, Tan B. Construction of Tropane Derivatives by the Organocatalytic Asymmetric Dearomatization of Isoquinolines. Angewandte Chemie (International Ed. in English). PMID 27599657 DOI: 10.1002/Anie.201605736 |
0.533 |
|
| 2016 |
Lin JS, Dong XY, Li TT, Jiang NC, Tan B, Liu XY. A Dual-Catalytic Strategy to Direct Asymmetric Radical Aminotrifluoromethylation of Alkenes. Journal of the American Chemical Society. PMID 27414501 DOI: 10.1021/Jacs.6B04077 |
0.46 |
|
| 2016 |
Zhang JW, Xu JH, Cheng DJ, Shi C, Liu XY, Tan B. Discovery and enantiocontrol of axially chiral urazoles via organocatalytic tyrosine click reaction. Nature Communications. 7: 10677. PMID 26864510 DOI: 10.1038/Ncomms10677 |
0.537 |
|
| 2016 |
Yang NY, Li ZL, Ye L, Tan B, Liu XY. Organic base-catalysed solvent-tuned chemoselective carbotrifluoromethylation and oxytrifluoromethylation of unactivated alkenes. Chemical Communications (Cambridge, England). PMID 26854124 DOI: 10.1039/C6Cc00364H |
0.35 |
|
| 2016 |
Ma CL, Li XH, Yu XL, Zhu XL, Hu YZ, Dong XW, Tan B, Liu XY. Gold-catalyzed tandem synthesis of bioactive spiro-dipyrroloquinolines and its application in the one-step synthesis of incargranine B aglycone and seneciobipyrrolidine (I) Organic Chemistry Frontiers. 3: 324-329. DOI: 10.1039/C5Qo00354G |
0.478 |
|
| 2016 |
Yu XL, Kuang L, Chen S, Zhu XL, Li ZL, Tan B, Liu XY. Counteranion-Controlled Unprecedented Diastereo- and Enantioselective Tandem Formal Povarov Reaction for Construction of Bioactive Octahydro-Dipyrroloquinolines Acs Catalysis. 6: 6182-6190. DOI: 10.1021/Acscatal.6B01492 |
0.479 |
|
| 2015 |
Chen YH, Cheng DJ, Zhang J, Wang Y, Liu XY, Tan B. Atroposelective Synthesis of Axially Chiral Biaryldiols via Organocatalytic Arylation of 2-Naphthols. Journal of the American Chemical Society. PMID 26560999 DOI: 10.1021/Jacs.5B10152 |
0.543 |
|
| 2015 |
Zhang J, Lin SX, Cheng DJ, Liu XY, Tan B. Phosphoric Acid-Catalyzed Asymmetric Classic Passerini Reaction. Journal of the American Chemical Society. PMID 26488384 DOI: 10.1021/Jacs.5B09117 |
0.51 |
|
| 2015 |
Liu S, Tan B, Dai C, Lou S, Tao A, Zhong G. Geochemical characterization and heavy metal migration in a coastal polluted aquifer incorporating tidal effects: field investigation in Chongming Island, China. Environmental Science and Pollution Research International. PMID 26300351 DOI: 10.1007/s11356-015-5010-9 |
0.358 |
|
| 2015 |
Wu MY, He WW, Liu XY, Tan B. Asymmetric Construction of Spirooxindoles by Organocatalytic Multicomponent Reactions Using Diazooxindoles. Angewandte Chemie (International Ed. in English). PMID 26136346 DOI: 10.1002/Anie.201504640 |
0.507 |
|
| 2015 |
Fang ZJ, Zheng SC, Guo Z, Guo JY, Tan B, Liu XY. Asymmetric Synthesis of Axially Chiral Isoquinolones: Nickel-Catalyzed Denitrogenative Transannulation. Angewandte Chemie (International Ed. in English). PMID 26119725 DOI: 10.1002/Anie.201503207 |
0.514 |
|
| 2015 |
Lin JS, Yu P, Huang L, Zhang P, Tan B, Liu XY. Brønsted Acid Catalyzed Asymmetric Hydroamination of Alkenes: Synthesis of Pyrrolidines Bearing a Tetrasubstituted Carbon Stereocenter. Angewandte Chemie (International Ed. in English). 54: 7847-51. PMID 26013971 DOI: 10.1002/Anie.201501762 |
0.453 |
|
| 2015 |
Huang L, Zheng SC, Tan B, Liu XY. Trifluoromethylation-initiated remote cross-coupling of carbonyl compounds to form carbon-heteroatom/carbon bonds. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 6718-22. PMID 25766396 DOI: 10.1002/Chem.201500629 |
0.402 |
|
| 2015 |
Huang L, Zheng SC, Tan B, Liu XY. Metal-free direct 1,6- and 1,2-difunctionalization triggered by radical trifluoromethylation of alkenes. Organic Letters. 17: 1589-92. PMID 25763688 DOI: 10.1021/Acs.Orglett.5B00479 |
0.342 |
|
| 2015 |
Yu P, Zheng SC, Yang NY, Tan B, Liu XY. Phosphine-catalyzed remote β-C-H functionalization of amines triggered by trifluoromethylation of alkenes: one-pot synthesis of bistrifluoromethylated enamides and oxazoles. Angewandte Chemie (International Ed. in English). 54: 4041-5. PMID 25694337 DOI: 10.1002/Anie.201412310 |
0.474 |
|
| 2015 |
Huang L, Lin JS, Tan B, Liu XY. Alkene trifluoromethylation-initiated remote α-azidation of carbonyl compounds toward trifluoromethyl γ-lactam and spirobenzofuranone-lactam Acs Catalysis. 5: 2826-2831. DOI: 10.1021/Acscatal.5B00311 |
0.394 |
|
| 2015 |
Liu S, Tan B, Dai C, Lou S, Tao A, Zhong G. Geochemical characterization and heavy metal migration in a coastal polluted aquifer incorporating tidal effects: field investigation in Chongming Island, China Environmental Science and Pollution Research. DOI: 10.1007/s11356-015-5010-9 |
0.36 |
|
| 2015 |
Ma C, Yu X, Zhu X, Hu Y, Dong X, Tan B, Liu X. ChemInform Abstract: Platinum-Catalyzed Tandem Cyclization Reaction to Multiply Substituted Indolines under Microwave-Assisted Conditions. Cheminform. 46: no-no. DOI: 10.1002/chin.201526138 |
0.385 |
|
| 2015 |
Yu P, Zheng S, Yang N, Tan B, Liu X. Back Cover: Phosphine‐Catalyzed Remote β‐CH Functionalization of Amines Triggered by Trifluoromethylation of Alkenes: One‐Pot Synthesis of Bistrifluoromethylated Enamides and Oxazoles (Angew. Chem. Int. Ed. 13/2015) Angewandte Chemie. 54: 4126-4126. DOI: 10.1002/Anie.201501767 |
0.392 |
|
| 2015 |
Ma C, Yu X, Zhu X, Hu Y, Dong X, Tan B, Liu X. Platinum-Catalyzed Tandem Cyclization Reaction to Multiply Substituted Indolines under Microwave-Assisted Conditions Advanced Synthesis & Catalysis. 357: 569-575. DOI: 10.1002/Adsc.201400933 |
0.508 |
|
| 2014 |
Li L, Guo JY, Liu XG, Chen S, Wang Y, Tan B, Liu XY. Amide groups switch selectivity: C-H trifluoromethylation of α,β-unsaturated amides and subsequent asymmetric transformation. Organic Letters. 16: 6032-5. PMID 25383919 DOI: 10.1021/Ol503067G |
0.383 |
|
| 2014 |
Yu P, Lin JS, Li L, Zheng SC, Xiong YP, Zhao LJ, Tan B, Liu XY. Enantioselective C-H bond functionalization triggered by radical trifluoromethylation of unactivated alkene. Angewandte Chemie (International Ed. in English). 53: 11890-4. PMID 25201806 DOI: 10.1002/Anie.201405401 |
0.435 |
|
| 2014 |
Lin JS, Liu XG, Zhu XL, Tan B, Liu XY. Copper-catalyzed aminotrifluoromethylation of unactivated alkenes with (TMS)CF3: construction of trifluoromethylated azaheterocycles. The Journal of Organic Chemistry. 79: 7084-92. PMID 25002033 DOI: 10.1021/Jo5012619 |
0.374 |
|
| 2014 |
Zhu XL, Xu JH, Cheng DJ, Zhao LJ, Liu XY, Tan B. In situ generation of electrophilic trifluoromethylthio reagents for enantioselective trifluoromethylthiolation of oxindoles. Organic Letters. 16: 2192-5. PMID 24697212 DOI: 10.1021/Ol5006888 |
0.524 |
|
| 2014 |
Cheng DJ, Yan L, Tian SK, Wu MY, Wang LX, Fan ZL, Zheng SC, Liu XY, Tan B. Highly enantioselective kinetic resolution of axially chiral BINAM derivatives catalyzed by a Brønsted acid. Angewandte Chemie (International Ed. in English). 53: 3684-7. PMID 24591330 DOI: 10.1002/Anie.201310562 |
0.482 |
|
| 2014 |
Xiong YP, Wu MY, Zhang XY, Ma CL, Huang L, Zhao LJ, Tan B, Liu XY. Direct access to α-trifluoromethyl enones via efficient copper-catalyzed trifluoromethylation of Meyer-Schuster rearrangement. Organic Letters. 16: 1000-3. PMID 24467612 DOI: 10.1021/Ol403741M |
0.468 |
|
| 2014 |
Lin JS, Xiong YP, Ma CL, Zhao LJ, Tan B, Liu XY. Efficient copper-catalyzed direct intramolecular aminotrifluoromethylation of unactivated alkenes with diverse nitrogen-based nucleophiles. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 1332-40. PMID 24458913 DOI: 10.1002/Chem.201303387 |
0.499 |
|
| 2014 |
Tan B, Zhang X, Zhong G. Protecting-group directed stereospecific organocatalytic [3+2] cycloadditions: A facile access to chiral spirocyclic oxindoles Arkivoc. 2014: 124-142. DOI: 10.3998/Ark.5550190.P008.401 |
0.587 |
|
| 2014 |
Cheng D, Ishihara Y, Tan B, Barbas CF. Organocatalytic asymmetric assembly reactions: Synthesis of spirooxindoles via organocascade strategies Acs Catalysis. 4: 743-762. DOI: 10.1021/Cs401172R |
0.437 |
|
| 2014 |
Cheng D, Ishihara Y, Tan B, Barbas CF. ChemInform Abstract: Organocatalytic Asymmetric Assembly Reactions: Synthesis of Spirooxindoles via Organocascade Strategies Cheminform. 45: no-no. DOI: 10.1002/chin.201418275 |
0.379 |
|
| 2013 |
Jiang X, Tan B, Barbas CF. Core-structure-motivated design of iminium-enolate organocascade reactions: enantioselective syntheses of 5,6-dihydroindolizines. Angewandte Chemie (International Ed. in English). 52: 9261-5. PMID 23843168 DOI: 10.1002/Anie.201303300 |
0.428 |
|
| 2013 |
Albertshofer K, Tan B, Barbas CF. Asymmetric construction of spirocyclopentenebenzofuranone core structures via highly selective phosphine-catalyzed [3 + 2] cycloaddition reactions. Organic Letters. 15: 2958-61. PMID 23730934 DOI: 10.1021/Ol401087A |
0.521 |
|
| 2012 |
Tan B, Toda N, Barbas CF. Organocatalytic amidation and esterification of aldehydes with activating reagents by a cross-coupling strategy. Angewandte Chemie (International Ed. in English). 51: 12538-41. PMID 23135813 DOI: 10.1002/Anie.201205921 |
0.429 |
|
| 2012 |
Tan B, Hernández-Torres G, Barbas CF. Rationally designed amide donors for organocatalytic asymmetric Michael reactions. Angewandte Chemie (International Ed. in English). 51: 5381-5. PMID 22505348 DOI: 10.1002/Anie.201200996 |
0.416 |
|
| 2012 |
Hernández-Torres G, Tan B, Barbas CF. Organocatalysis as a safe practical method for the stereospecific dibromination of unsaturated compounds. Organic Letters. 14: 1858-61. PMID 22443632 DOI: 10.1021/Ol300456X |
0.487 |
|
| 2012 |
Albertshofer K, Tan B, Barbas CF. Assembly of spirooxindole derivatives containing four consecutive stereocenters via organocatalytic Michael-Henry cascade reactions. Organic Letters. 14: 1834-7. PMID 22436132 DOI: 10.1021/Ol300441Z |
0.527 |
|
| 2012 |
Tan B, Zeng X, Leong WW, Shi Z, Barbas CF, Zhong G. Core structure-based design of organocatalytic [3+2]-cycloaddition reactions: highly efficient and stereocontrolled syntheses of 3,3'-pyrrolidonyl spirooxindoles. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 63-7. PMID 22162076 DOI: 10.1002/Chem.201103449 |
0.582 |
|
| 2011 |
Tan B, Hernández-Torres G, Barbas CF. Highly efficient hydrogen-bonding catalysis of the Diels-Alder reaction of 3-vinylindoles and methyleneindolinones provides carbazolespirooxindole skeletons. Journal of the American Chemical Society. 133: 12354-7. PMID 21780763 DOI: 10.1021/Ja203812H |
0.48 |
|
| 2011 |
Tan B, Candeias NR, Barbas CF. Construction of bispirooxindoles containing three quaternary stereocentres in a cascade using a single multifunctional organocatalyst. Nature Chemistry. 3: 473-7. PMID 21602863 DOI: 10.1038/Nchem.1039 |
0.513 |
|
| 2011 |
Tan B, Candeias NR, Barbas CF. Core-structure-motivated design of a phosphine-catalyzed [3+2] cycloaddition reaction: enantioselective syntheses of spirocyclopenteneoxindoles. Journal of the American Chemical Society. 133: 4672-5. PMID 21395245 DOI: 10.1021/Ja110147W |
0.517 |
|
| 2010 |
Shi Z, Tan B, Leong WW, Zeng X, Lu M, Zhong G. Catalytic asymmetric formal [4 + 1] annulation leading to optically active cis-isoxazoline N-oxides. Organic Letters. 12: 5402-5. PMID 20958089 DOI: 10.1021/Ol102181R |
0.501 |
|
| 2010 |
Chua PJ, Tan B, Yang L, Zeng X, Zhu D, Zhong G. Highly stereoselective synthesis of indanes with four stereogenic centers via sequential Michael reaction and [3+2] cycloaddition. Chemical Communications (Cambridge, England). 46: 7611-3. PMID 20838691 DOI: 10.1039/C0Cc01577F |
0.667 |
|
| 2010 |
Tan B, Lu Y, Zeng X, Chua PJ, Zhong G. Facile domino access to chiral bicyclo[3.2.1]octanes and discovery of a new catalytic activation mode. Organic Letters. 12: 2682-5. PMID 20469881 DOI: 10.1021/Ol1007795 |
0.581 |
|
| 2010 |
Zeng X, Ye K, Lu M, Chua PJ, Tan B, Zhong G. Chiral Brønsted acid catalyzed enantioselective addition of alpha-isocyanoacetamides to aldehydes. Organic Letters. 12: 2414-7. PMID 20429535 DOI: 10.1021/Ol1007789 |
0.6 |
|
| 2010 |
Xu ZJ, Zhu D, Zeng X, Wang F, Tan B, Hou Y, Lv Y, Zhong G. Diastereoselective HOTf-catalyzed three-component one-pot 1,3-dipolar cycloaddition of alpha-diazo ester, nitrosobenzene and electron-deficient alkene. Chemical Communications (Cambridge, England). 46: 2504-6. PMID 20309476 DOI: 10.1039/B924575H |
0.564 |
|
| 2010 |
Tan B, Zhu D, Zhang L, Chua PJ, Zeng X, Zhong G. Water--more than just a green solvent: a stereoselective one-pot access to all-chiral tetrahydronaphthalenes in aqueous media. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 3842-8. PMID 20151437 DOI: 10.1002/Chem.200902932 |
0.603 |
|
| 2009 |
Chua PJ, Tan B, Zeng X, Zhong G. L-prolinol as a highly enantioselective catalyst for Michael addition of cyclohexanone to nitroolefins. Bioorganic & Medicinal Chemistry Letters. 19: 3915-8. PMID 19359171 DOI: 10.1016/J.Bmcl.2009.03.076 |
0.591 |
|
| 2009 |
Tan B, Zeng X, Lu Y, Chua PJ, Zhong G. Rational design of organocatalyst: highly stereoselective Michael addition of cyclic ketones to nitroolefins. Organic Letters. 11: 1927-30. PMID 19344184 DOI: 10.1021/Ol900330P |
0.611 |
|
| 2009 |
Tan B, Zhang X, Chua PJ, Zhong G. Recyclable organocatalysis: highly enantioselective Michael addition of 1,3-diaryl-1,3-propanedione to nitroolefins. Chemical Communications (Cambridge, England). 779-81. PMID 19322439 DOI: 10.1039/B813915F |
0.597 |
|
| 2009 |
Lu M, Zhu D, Lu Y, Zeng X, Tan B, Xu Z, Zhong G. Chiral Brønsted acid-catalyzed enantioselective alpha-hydroxylation of beta-dicarbonyl compounds. Journal of the American Chemical Society. 131: 4562-3. PMID 19290662 DOI: 10.1021/Ja8088907 |
0.512 |
|
| 2009 |
Yang L, Tan B, Wang F, Zhong G. An unexpected N-heterocyclic carbene-catalyzed annulation of enals and nitroso compounds. The Journal of Organic Chemistry. 74: 1744-6. PMID 19170534 DOI: 10.1021/Jo802515G |
0.538 |
|
| 2009 |
Tan B, Shi Z, Chua PJ, Li Y, Zhong G. Unusual domino michael/aldol condensation reactions employing oximes as N-selective nucleophiles: synthesis of N-hydroxypyrroles. Angewandte Chemie (International Ed. in English). 48: 758-61. PMID 19130437 DOI: 10.1002/Anie.200805205 |
0.577 |
|
| 2009 |
Chua PJ, Tan B, Zhong G. Highly enantioselective l-thiaproline catalyzed α-aminoxylation of aldehydes in aqueous media Green Chemistry. 11: 543-547. DOI: 10.1039/B817950F |
0.553 |
|
| 2009 |
Chua PJ, Tan B, Zhong G. ChemInform Abstract: Highly Enantioselective L-Thiaproline Catalyzed α-Aminoxylation of Aldehydes in Aqueous Media. Cheminform. 40. DOI: 10.1002/chin.200934059 |
0.482 |
|
| 2008 |
Lu M, Zhu D, Lu Y, Hou Y, Tan B, Zhong G. Organocatalytic Asymmetric α‐Aminoxylation/Aza‐Michael Reactions for the Synthesis of Functionalized Tetrahydro‐1,2‐oxazines Angewandte Chemie. 47: 10013-10013. PMID 19072787 DOI: 10.1002/Anie.200890274 |
0.624 |
|
| 2008 |
Lu M, Zhu D, Lu Y, Hou Y, Tan B, Zhong G. Organocatalytic asymmetric alpha-aminoxylation/aza-Michael reactions for the synthesis of functionalized tetrahydro-1,2-oxazines. Angewandte Chemie (International Ed. in English). 47: 10187-91. PMID 18846534 DOI: 10.1002/anie.200803731 |
0.544 |
|
| 2008 |
Zhu D, Lu M, Chua PJ, Tan B, Wang F, Yang X, Zhong G. A highly stereoselective organocatalytic tandem aminoxylation/aza-Michael reaction for the synthesis of tetrahydro-1,2-oxazines. Organic Letters. 10: 4585-8. PMID 18788743 DOI: 10.1021/Ol801864C |
0.634 |
|
| 2008 |
Tan B, Chua PJ, Zeng X, Lu M, Zhong G. A highly diastereo- and enantioselective synthesis of multisubstituted cyclopentanes with four chiral carbons by the organocatalytic domino Michael-Henry reaction. Organic Letters. 10: 3489-92. PMID 18630924 DOI: 10.1021/Ol801273X |
0.646 |
|
| 2008 |
Tan B, Shi Z, Chua PJ, Zhong G. Control of four stereocenters in an organocatalytic domino double Michael reaction: efficient synthesis of multisubstituted cyclopentanes. Organic Letters. 10: 3425-8. PMID 18616339 DOI: 10.1021/Ol801246M |
0.664 |
|
| 2008 |
Tan B, Chua PJ, Li Y, Zhong G. Organocatalytic asymmetric tandem Michael-Henry reactions: a highly stereoselective synthesis of multifunctionalized cyclohexanes with two quaternary stereocenters. Organic Letters. 10: 2437-40. PMID 18489178 DOI: 10.1021/Ol8007183 |
0.666 |
|
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