| Year |
Citation |
Score |
| 2023 |
Zhu GH, Jiang X. Rh(I)-Catalyzed Cascade Carbonylative Cyclization of Propargyl α-Diazoindolacetates for Construction of Carbazoles. Organic Letters. 25: 8077-8082. PMID 37933919 DOI: 10.1021/acs.orglett.3c03132 |
0.308 |
|
| 2021 |
Zhu G, Gao WC, Jiang X. Rh(I)-Catalyzed Carbene Migration/Carbonylation/Cyclization: Straightforward Construction of Fully Substituted Aryne Precursors. Journal of the American Chemical Society. PMID 33439011 DOI: 10.1021/jacs.0c13012 |
0.362 |
|
| 2020 |
Xue J, Jiang X. Unsymmetrical polysulfidation via designed bilateral disulfurating reagents. Nature Communications. 11: 4170. PMID 32820174 DOI: 10.1038/S41467-020-18029-Z |
0.367 |
|
| 2020 |
Li Y, Chen S, Wang M, Jiang X. Sodium Dithionite-Mediated Decarboxylative Sulfonylation: Facile Access to Tertiary Sulfones. Angewandte Chemie (International Ed. in English). PMID 32149440 DOI: 10.1002/Anie.202001589 |
0.396 |
|
| 2020 |
Lu L, Li Y, Jiang X. Visible-light-promoted oxidative halogenation of (hetero)arenes Green Chemistry. DOI: 10.1039/D0Gc02091E |
0.352 |
|
| 2020 |
Chen S, Li Y, Wang M, Jiang X. General sulfone construction via sulfur dioxide surrogate control Green Chemistry. 22: 322-326. DOI: 10.1039/C9Gc03841H |
0.363 |
|
| 2020 |
Cheng R, Wu L, Lai R, Peng C, Naowarojna N, Hu W, Li X, Whelan SA, Lee N, Lopez J, Zhao C, Yong Y, Xue J, Jiang X, Grinstaff MW, et al. Single-Step Replacement of an Unreactive C–H Bond by a C–S Bond Using Polysulfide as the Direct Sulfur Source in the Anaerobic Ergothioneine Biosynthesis Acs Catalysis. 10: 8981-8994. DOI: 10.1021/Acscatal.0C01809 |
0.305 |
|
| 2019 |
Li Y, Mou T, Lu L, Jiang X. Visible-light-promoted oxidative halogenation of alkynes. Chemical Communications (Cambridge, England). PMID 31712789 DOI: 10.1039/C9Cc07655G |
0.329 |
|
| 2019 |
Meng Y, Wang M, Jiang X. Inorganic Sulfur Dioxide Surrogate-Involved Multicomponent Reductive Cross-Coupling: A Straightforward Functional Sulfone Construction and Linkage. Angewandte Chemie (International Ed. in English). PMID 31670894 DOI: 10.1002/Anie.201911449 |
0.416 |
|
| 2019 |
Tan W, Jänsch N, Öhlmann T, Meyer-Almes FJ, Jiang X. Thiocarbonyl Surrogate via Combination of Potassium Sulfide and Chloroform for Dithiocarbamate Construction. Organic Letters. PMID 31497974 DOI: 10.1021/Acs.Orglett.9B02784 |
0.387 |
|
| 2019 |
Li Y, Rizvi AE, Hu D, Sun D, Gao A, Zhou Y, Li J, Jiang X. Selective Late-Stage Oxygenation with Ground-State Oxygen Based on Sulfides by Uranyl Photocatalysis. Angewandte Chemie (International Ed. in English). PMID 31301096 DOI: 10.1002/Anie.201906080 |
0.309 |
|
| 2019 |
Wang M, Dai Z, Jiang X. Design and application of α-ketothioesters as 1,2-dicarbonyl-forming reagents. Nature Communications. 10: 2661. PMID 31209228 DOI: 10.1038/S41467-019-10651-W |
0.394 |
|
| 2019 |
Wang N, Saidhareddy P, Jiang X. Construction of sulfur-containing moieties in the total synthesis of natural products. Natural Product Reports. PMID 31204423 DOI: 10.1039/C8Np00093J |
0.364 |
|
| 2019 |
Wang M, Zhao J, Jiang X. Aryl Methyl Sulfone Construction from Eco-Friendly Inorganic Sulfur Dioxide and Methyl Reagents. Chemsuschem. PMID 30680940 DOI: 10.1002/Cssc.201802919 |
0.347 |
|
| 2019 |
Liu Y, Ling H, Chen C, Xu Q, Yu L, Jiang X. Sodium Selenosulfate from Sodium Sulfite and Selenium Powder: An Odorless Selenylating Reagent for Alkyl Halides to Produce Dialkyl Diselenide Catalysts Synlett. 30: 1698-1702. DOI: 10.1055/S-0037-1612083 |
0.404 |
|
| 2019 |
Shao L, Li Y, Lu J, Jiang X. Recent progress in selenium-catalyzed organic reactions Organic Chemistry Frontiers. 6: 2999-3041. DOI: 10.1039/C9Qo00620F |
0.392 |
|
| 2018 |
Wang M, Qiao Z, Zhao J, Jiang X. Palladium-Catalyzed Thiomethylation via a Three-Component Cross-Coupling Strategy. Organic Letters. PMID 30216075 DOI: 10.1021/Acs.Orglett.8B02677 |
0.379 |
|
| 2018 |
Wang Y, Li Y, Jiang X. Sulfur-Center-Involved Photocatalyzed Reactions. Chemistry, An Asian Journal. PMID 29968355 DOI: 10.1002/Asia.201800532 |
0.424 |
|
| 2018 |
Wang M, Chen S, Jiang X. The Recent Progress of Atom-Economical Applications of Diaryliodonium Salt. Chemistry, An Asian Journal. PMID 29901850 DOI: 10.1002/Asia.201800609 |
0.421 |
|
| 2018 |
Xiao X, Xue J, Jiang X. Polysulfurating reagent design for unsymmetrical polysulfide construction. Nature Communications. 9: 2191. PMID 29875443 DOI: 10.1038/S41467-018-04306-5 |
0.354 |
|
| 2018 |
Ding D, Zhu G, Jiang X. Ligand Controlled Pd(II)-Catalyzed Regiodivergent Carbonylation of Alkynes for Syntheses of Indolo[3,2-c]coumarins and Benzofuro[3,2-c]quinolinones. Angewandte Chemie (International Ed. in English). PMID 29851274 DOI: 10.1002/Anie.201804788 |
0.362 |
|
| 2018 |
Wang M, Jiang X. Sulfur-Sulfur Bond Construction. Topics in Current Chemistry (Cham). 376: 14. PMID 29637310 DOI: 10.1007/S41061-018-0192-5 |
0.375 |
|
| 2018 |
Wang M, Jiang X. The recycling of sulfur dioxide Chinese Science Bulletin. 63: 2707-2716. DOI: 10.1360/N972018-00606 |
0.422 |
|
| 2018 |
Tan W, Wang C, Jiang X. Green carbon disulfide surrogate via a combination of potassium sulfide and chloroform for benzothiazine-thione and benzothiazole-thione construction Organic Chemistry Frontiers. 5: 2390-2394. DOI: 10.1039/C8Qo00481A |
0.365 |
|
| 2018 |
Song J, Liu Q, Liu H, Jiang X. Recent Advances in Palladium‐Catalyzed Carboxylation with CO2 European Journal of Organic Chemistry. 2018: 696-713. DOI: 10.1002/Ejoc.201701436 |
0.343 |
|
| 2018 |
Chen S, Wang M, Jiang X. Pd-Catalyzed C-S Cyclization via C-H Functionalization Strategy: Access to Sulfur-containing Benzoheterocyclics Chinese Journal of Chemistry. 36: 921-924. DOI: 10.1002/Cjoc.201800242 |
0.329 |
|
| 2017 |
Wang N, Liu J, Wang C, Bai L, Jiang X. Asymmetric Total Syntheses of (-)-Jerantinines A, C, and E, (-)-16-Methoxytabersonine, (-)-Vindoline, and (+)-Vinblastine. Organic Letters. PMID 29272137 DOI: 10.1021/Acs.Orglett.7B03694 |
0.419 |
|
| 2017 |
Wang M, Fan Q, Jiang X. Nitrogen-Iodine Exchange of Diaryliodonium Salts: Access to Acridine and Carbazole. Organic Letters. PMID 29256611 DOI: 10.1021/Acs.Orglett.7B03564 |
0.322 |
|
| 2017 |
Wang M, Chen S, Jiang X. Construction of Functionalized Annulated Sulfone via SO2/I Exchange of Cyclic Diaryliodonium Salts. Organic Letters. PMID 28876937 DOI: 10.1021/Acs.Orglett.7B02388 |
0.348 |
|
| 2017 |
Wang N, Du S, Li D, Jiang X. Divergent Asymmetric Total Synthesis of (+)-Vincadifformine, (-)-Quebrachamine, (+)-Aspidospermidine, (-)-Aspidospermine, (-)-Pyrifolidine, and Related Natural Products. Organic Letters. PMID 28570070 DOI: 10.1021/Acs.Orglett.7B01292 |
0.384 |
|
| 2017 |
Ding D, Mou T, Xue J, Jiang X. Access to divergent benzo-heterocycles via a catalyst-dependent strategy in the controllable cyclization of o-alkynyl-N-methoxyl-benzamides. Chemical Communications (Cambridge, England). PMID 28443851 DOI: 10.1039/C7Cc01861D |
0.336 |
|
| 2017 |
Tan W, Wei J, Jiang X. Thiocarbonyl Surrogate via Combination of Sulfur and Chloroform for Thiocarbamide and Oxazolidinethione Construction. Organic Letters. PMID 28388051 DOI: 10.1021/Acs.Orglett.7B00819 |
0.355 |
|
| 2017 |
Qiao Z, Jiang X. Recent developments in sulfur-carbon bond formation reaction involving thiosulfates. Organic & Biomolecular Chemistry. PMID 28177013 DOI: 10.1039/C6Ob02833K |
0.363 |
|
| 2017 |
Wang M, Wei J, Fan Q, Jiang X. Cu(ii)-catalyzed sulfide construction: both aryl groups utilization of intermolecular and intramolecular diaryliodonium salt. Chemical Communications (Cambridge, England). PMID 28165512 DOI: 10.1039/C6Cc09201B |
0.369 |
|
| 2017 |
Jiang X. Sulfur atom transfer (SAT) reaction Phosphorus Sulfur and Silicon and the Related Elements. 192: 169-171. DOI: 10.1080/10426507.2016.1250762 |
0.328 |
|
| 2017 |
Li Y, Wang M, Jiang X. Controllable Sulfoxidation and Sulfenylation with Organic Thiosulfate Salts via Dual Electron- and Energy-Transfer Photocatalysis Acs Catalysis. 7: 7587-7592. DOI: 10.1021/Acscatal.7B02735 |
0.301 |
|
| 2017 |
Dai Z, Xiao X, Jiang X. Nucleophilic disulfurating reagents for unsymmetrical disulfides construction via copper-catalyzed oxidative cross coupling Tetrahedron. 73: 3702-3706. DOI: 10.1016/J.Tet.2017.05.010 |
0.373 |
|
| 2017 |
Liu M, Li Y, Yu L, Xu Q, Jiang X. Visible light-promoted, iodine-catalyzed selenoalkoxylation of olefins with diselenides and alcohols in the presence of hydrogen peroxide/air oxidant: an efficient access to α-alkoxyl selenides Science China Chemistry. 61: 294-299. DOI: 10.1007/S11426-017-9158-Y |
0.357 |
|
| 2016 |
Wang M, Fan Q, Jiang X. Transition-Metal-Free Diarylannulated Sulfide and Selenide Construction via Radical/Anion-Mediated Sulfur-Iodine and Selenium-Iodine Exchange. Organic Letters. PMID 27783528 DOI: 10.1021/Acs.Orglett.6B03078 |
0.319 |
|
| 2016 |
Xiao X, Feng M, Jiang X. New Design of a Disulfurating Reagent: Facile and Straightforward Pathway to Unsymmetrical Disulfanes by Copper-Catalyzed Oxidative Cross-Coupling. Angewandte Chemie (International Ed. in English). PMID 27726267 DOI: 10.1002/Anie.201608011 |
0.414 |
|
| 2016 |
Feng M, Tang B, Xu HX, Jiang X. Collective Synthesis of Phenanthridinone through C-H Activation Involving a Pd-Catalyzed Aryne Multicomponent Reaction. Organic Letters. PMID 27529796 DOI: 10.1021/Acs.Orglett.6B02109 |
0.461 |
|
| 2016 |
Ding D, Mou T, Feng M, Jiang X. Utility of Ligand Effect in Homogenous Gold Catalysis: Enabling Regiodivergent π-bond-activated Cyclization. Journal of the American Chemical Society. PMID 27058740 DOI: 10.1021/Jacs.6B01707 |
0.346 |
|
| 2016 |
Qiao Z, Jiang X. Ligand-Controlled Divergent Cross-Coupling Involving Organosilicon Compounds for Thioether and Thioester Synthesis. Organic Letters. PMID 26974172 DOI: 10.1021/Acs.Orglett.6B00324 |
0.37 |
|
| 2016 |
Wei J, Li Y, Jiang X. Aqueous Compatible Protocol to Both Alkyl and Aryl Thioamide Synthesis. Organic Letters. PMID 26734786 DOI: 10.1021/Acs.Orglett.5B03541 |
0.405 |
|
| 2016 |
Wang M, Wei J, Fan Q, Jiang X. A practical synthesis of novel chiral sulfoxide-nitrogen ligands Tetrahedron. 72: 2671-2676. DOI: 10.1016/J.Tet.2015.08.004 |
0.339 |
|
| 2016 |
Zhang Z, Dai Z, Jiang X. A General Strategy for Synthesis of Heterocyclic Hemiketal-Containing α,β-Unsaturated Ketones from Ynediones Asian Journal of Organic Chemistry. 5: 52-56. DOI: 10.1002/Ajoc.201500398 |
0.374 |
|
| 2015 |
Feng M, Tang B, Wang N, Xu HX, Jiang X. Ligand Controlled Regiodivergent C1 Insertion on Arynes for Construction of Phenanthridinone and Acridone Alkaloids. Angewandte Chemie (International Ed. in English). PMID 26478001 DOI: 10.1002/Anie.201508340 |
0.375 |
|
| 2015 |
Li Y, Xie W, Jiang X. Mechanistic Study of a Photocatalyzed CS Bond Formation Involving Alkyl/Aryl Thiosulfate. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26404539 DOI: 10.1002/Chem.201502951 |
0.407 |
|
| 2015 |
Feng M, Tang B, Liang SH, Jiang X. Sulfur Containing Scaffolds in Drugs: Synthesis and Application in Medicinal Chemistry. Current Topics in Medicinal Chemistry. PMID 26369815 DOI: 10.2174/1568026615666150915111741 |
0.339 |
|
| 2015 |
Qiao Z, Ge N, Jiang X. CO2-promoted oxidative cross-coupling reaction for C-S bond formation via masked strategy in an odourless way. Chemical Communications (Cambridge, England). 51: 10295-8. PMID 26022891 DOI: 10.1039/C5Cc03038B |
0.382 |
|
| 2015 |
Xiao X, Feng M, Jiang X. Transition-metal-free persulfuration to construct unsymmetrical disulfides and mechanistic study of the sulfur redox process. Chemical Communications (Cambridge, England). 51: 4208-11. PMID 25604049 DOI: 10.1039/C4Cc09633A |
0.314 |
|
| 2015 |
Zhang Y, Li Y, Zhang X, Jiang X. Sulfide synthesis through copper-catalyzed C-S bond formation under biomolecule-compatible conditions. Chemical Communications (Cambridge, England). 51: 941-4. PMID 25435202 DOI: 10.1039/C4Cc08367A |
0.448 |
|
| 2015 |
Zhang Z, Dai Z, Jiang X. Copper-Catalyzed Aerobic Oxidative Dicarbonylation of Indoles toward Solvatochromic Fluorescent Indole-Substituted Quinoxalines Asian Journal of Organic Chemistry. 4: 1370-1374. DOI: 10.1002/Ajoc.201500332 |
0.404 |
|
| 2014 |
Liu H, Feng M, Jiang X. Unstrained carbon-carbon bond cleavage. Chemistry, An Asian Journal. 9: 3360-89. PMID 25179561 DOI: 10.1002/Asia.201402591 |
0.32 |
|
| 2014 |
Zhang Z, Jiang X. Oxidative coupling of terminal alkyne with α-hydroxy ketone: an expedient approach toward ynediones. Organic Letters. 16: 4400-3. PMID 25127422 DOI: 10.1021/Ol502298A |
0.389 |
|
| 2014 |
Feng M, Jiang X. Stereoselective construction of a key hydroindole precursor of epidithiodiketopiperazine (ETP) natural products. Chemical Communications (Cambridge, England). 50: 9690-2. PMID 25017898 DOI: 10.1039/C4Cc04148H |
0.356 |
|
| 2014 |
Liu H, Wei J, Qiao Z, Fu Y, Jiang X. Palladium-catalyzed intramolecular reductive cross-coupling of Csp2-Csp3 bond formation. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 8308-13. PMID 24889494 DOI: 10.1002/Chem.201403093 |
0.355 |
|
| 2014 |
Li Y, Pu J, Jiang X. A highly efficient Cu-catalyzed S-transfer reaction: from amine to sulfide. Organic Letters. 16: 2692-5. PMID 24802853 DOI: 10.1021/Ol5009747 |
0.424 |
|
| 2014 |
Qiao Z, Wei J, Jiang X. Direct cross-coupling access to diverse aromatic sulfide: palladium-catalyzed double C-S bond construction using Na2S2O3 as a sulfurating reagent. Organic Letters. 16: 1212-5. PMID 24555790 DOI: 10.1021/Ol500112Y |
0.408 |
|
| 2014 |
Wang M, Feng M, Tang B, Jiang X. Recent advances of desymmetrization protocol applied in natural product total synthesis Tetrahedron Letters. 55: 7147-7155. DOI: 10.1016/J.Tetlet.2014.10.152 |
0.362 |
|
| 2013 |
Liu H, Jiang X. Transfer of sulfur: from simple to diverse. Chemistry, An Asian Journal. 8: 2546-63. PMID 23846983 DOI: 10.1002/Asia.201300636 |
0.431 |
|
| 2013 |
Qiao Z, Liu H, Xiao X, Fu Y, Wei J, Li Y, Jiang X. Efficient access to 1,4-benzothiazine: palladium-catalyzed double C-S bond formation using Na2S2O3 as sulfurating reagent. Organic Letters. 15: 2594-7. PMID 23659388 DOI: 10.1021/Ol400618K |
0.481 |
|
| 2013 |
Wang L, Huang J, Peng S, Liu H, Jiang X, Wang J. Palladium-catalyzed oxidative cycloaddition through C-H/N-H activation: access to benzazepines. Angewandte Chemie (International Ed. in English). 52: 1768-72. PMID 23281177 DOI: 10.1002/Anie.201208076 |
0.317 |
|
| 2013 |
Liu H, Gu Z, Jiang X. ChemInform Abstract: Direct Trifluoromethylation of the C-H Bond Cheminform. 44: no-no. DOI: 10.1002/chin.201329235 |
0.525 |
|
| 2013 |
Liu H, Gu Z, Jiang X. Direct Trifluoromethylation of the CH Bond Advanced Synthesis & Catalysis. 355: 617-626. DOI: 10.1002/Adsc.201200764 |
0.541 |
|
| 2012 |
Liu H, Dong C, Zhang Z, Wu P, Jiang X. Transition-metal-free aerobic oxidative cleavage of C-C bonds in α-hydroxy ketones and mechanistic insight to the reaction pathway. Angewandte Chemie (International Ed. in English). 51: 12570-4. PMID 23129361 DOI: 10.1002/Anie.201207206 |
0.375 |
|
| 2012 |
Jiang X, Shi L, Liu H, Khan AH, Chen JS. Gas extrusion in natural products total synthesis. Organic & Biomolecular Chemistry. 10: 8383-92. PMID 22940671 DOI: 10.1039/C2Ob26152A |
0.424 |
|
| 2012 |
Liu H, Qiao Z, Jiang X. Palladium-catalyzed atom transfer radical cyclization of unactivated alkyl iodide. Organic & Biomolecular Chemistry. 10: 7274-7. PMID 22886029 DOI: 10.1039/C2Ob25990G |
0.357 |
|
| 2012 |
Siau WY, Li W, Xue F, Ren Q, Wu M, Sun S, Guo H, Jiang X, Wang J. Catalytic and enantioselective α-functionalization of oxindoles through oxidative reactions with naphthoquinones. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 9491-5. PMID 22736517 DOI: 10.1002/Chem.201200206 |
0.371 |
|
| 2012 |
Ren Q, Huang J, Wang L, Li W, Liu H, Jiang X, Wang J. Highly Efficient Assembly of 3-Hydroxy Oxindole Scaffold via a Catalytic Decarboxylative [1,2]-Addition Strategy Acs Catalysis. 2: 2622-2625. DOI: 10.1021/Cs300628W |
0.359 |
|
| 2012 |
Li W, Liu H, Jiang X, Wang J. Enantioselective Organocatalytic Conjugate Addition of Nitroalkanes to Electrophilic 2-Iminochromenes Acs Catalysis. 2: 1535-1538. DOI: 10.1021/Cs300313J |
0.39 |
|
| 2012 |
Wan B, Jiang X, Jia G, Ma S. Electrophilic Cyclization of 2-(2′,3′-Allenyl)acetylacetates with Iodine Using Calcium Hydride as the Base European Journal of Organic Chemistry. 2012: 4373-4379. DOI: 10.1002/Ejoc.201200527 |
0.553 |
|
| 2012 |
Jiang X, Liu H, Gu Z. Carbon-Halogen Bond Formation by the Reductive Elimination of PdII Species Asian Journal of Organic Chemistry. 1: 16-24. DOI: 10.1002/Ajoc.201200035 |
0.637 |
|
| 2011 |
Cheng J, Jiang X, Ma S. Palladium-catalyzed approach to stereodefined ten-membered cycles from 1,5-bisallenes. Organic Letters. 13: 5200-3. PMID 21910412 DOI: 10.1021/Ol202074E |
0.554 |
|
| 2011 |
Nicolaou KC, Jiang X, Lindsay-Scott PJ, Corbu A, Yamashiro S, Bacconi A, Fowler VM. Total synthesis and biological evaluation of monorhizopodin and 16-epi-monorhizopodin. Angewandte Chemie (International Ed. in English). 50: 1139-44. PMID 21268213 DOI: 10.1002/Anie.201006780 |
0.407 |
|
| 2011 |
Cheng J, Jiang X, Zhu C, Ma S. ChemInform Abstract: Palladium-Catalyzed Three-Component Tandem Cyclization Reaction of 2-(2,3-Allenyl)acylacetates, Organic Halides, and Amines: An Effective Protocol for the Synthesis of 4,5-Dihydro-1H-pyrrole Derivatives. Cheminform. 42: no-no. DOI: 10.1002/chin.201149107 |
0.686 |
|
| 2011 |
Cheng J, Jiang X, Zhu C, Ma S. Palladium-Catalyzed Three-Component Tandem Cyclization Reaction of 2-(2,3-Allenyl)acylacetates, Organic Halides, and Amines: An Effective Protocol for the Synthesis of 4,5-Dihydro-1H-pyrrole Derivatives Advanced Synthesis & Catalysis. 353: 1676-1682. DOI: 10.1002/Adsc.201100002 |
0.678 |
|
| 2010 |
Chen G, Jiang X, Fu C, Ma S. The Diversified Reactivities of 1,5-Bisallenes Chemistry Letters. 39: 78-81. DOI: 10.1246/Cl.2010.78 |
0.396 |
|
| 2010 |
Chen G, Jiang X, Fu C, Ma S. ChemInform Abstract: The Diversified Reactivities of 1,5-Bisallenes Cheminform. 41: no-no. DOI: 10.1002/chin.201024223 |
0.35 |
|
| 2008 |
Jiang X, Kong W, Chen J, Ma S. Intermolecular sequential [4 + 2]-cycloaddition-aromatization reaction of aryl-substituted allenes with DMAD affording phenanthrene and naphthalene derivatives. Organic & Biomolecular Chemistry. 6: 3606-10. PMID 19082163 DOI: 10.1039/B808767A |
0.723 |
|
| 2008 |
Cheng X, Jiang X, Yu Y, Ma S. Efficient synthesis of 3-chloromethyl-2(5H)-furanones and 3-chloromethyl-5,6-dihydropyran-2-ones via the PdCl2-catalyzed chlorocyclocarbonylation of 2,3- or 3,4-allenols. The Journal of Organic Chemistry. 73: 8960-5. PMID 18939873 DOI: 10.1021/Jo8015677 |
0.535 |
|
| 2008 |
Jiang X, Ma X, Zheng Z, Ma S. Controllable cyclization reactions of 2-(2',3'-allenyl)acetylacetates catalyzed by gold and palladium affording substituted cyclopentene and 4,5-dihydrofuran derivatives with distinct selectivity. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 8572-8. PMID 18680128 DOI: 10.1002/Chem.200800793 |
0.565 |
|
| 2008 |
Jiang X, Ma S. ChemInform Abstract: trans-RhCl(CO)(PPh3)2-Catalyzed Monomeric and Dimeric Cycloisomerization of Propargylic 2,3-Dienoates. Establishment of α,β-Unsaturated δ-Lactone Rings by Cyclometallation. Cheminform. 39. DOI: 10.1002/chin.200804137 |
0.384 |
|
| 2007 |
Jiang X, Ma S. trans-RhCl(CO)(PPh3)2-catalyzed monomeric and dimeric cycloisomerization of propargylic 2,3-dienoates. Establishment of alpha,beta-unsaturated delta-lactone rings by cyclometallation. Journal of the American Chemical Society. 129: 11600-7. PMID 17725354 DOI: 10.1021/Ja073582U |
0.566 |
|
| 2007 |
Yang Q, Jiang X, Ma S. Highly diastereoselective palladium-catalyzed cyclizations of 3,4-allenylic hydrazines and organic halides -- highly stereoselective synthesis of optically active pyrazolidine derivatives and the prediction of the stereoselectivity. Chemistry (Weinheim An Der Bergstrasse, Germany). 13: 9310-6. PMID 17696188 DOI: 10.1002/Chem.200700620 |
0.517 |
|
| 2007 |
Ma S, Zheng Z, Jiang X. Pd(0)-catalyzed coupling-cyclization of 2-(2',3'-allenyl)acetylacetates and organic halides: an efficient synthesis of 4,5-dihydrofuran derivatives. Organic Letters. 9: 529-31. PMID 17249804 DOI: 10.1021/Ol0628917 |
0.541 |
|
| 2007 |
Jiang X, Ma S. Intramolecular [2 + 2]-Cycloaddition of Propargylic 2,3-Allenoates for the Efficient Synthesis of 3-Oxabicyclo[4.2.0]octa-1(8),5-dien-4-ones: A Dramatic Substituent Effect. Cheminform. 38. DOI: 10.1016/J.Tet.2007.05.040 |
0.548 |
|
| 2007 |
Ma S, Jiang X, Cheng X, Hou H. Highly Efficient Suzuki Coupling Reaction of α-Chloroalkylidene-β-lactones and β-Lactams with Organoboronic Acids. Cheminform. 38. DOI: 10.1002/chin.200708103 |
0.387 |
|
| 2006 |
Jiang X, Cheng X, Ma S. Controllable [2+2] cycloadditions of 1,5-bisallenyl-substituted compounds. Angewandte Chemie (International Ed. in English). 45: 8009-13. PMID 17083138 DOI: 10.1002/Anie.200602847 |
0.431 |
|
| 2006 |
Ma S, Jiang X, Cheng X, Hou H. Highly Efficient Suzuki Coupling Reaction of α-Chloroalkylidene-β-lactones and β-Lactams with Organoboronic Acids Advanced Synthesis & Catalysis. 348: 2114-2124. DOI: 10.1002/Adsc.200600234 |
0.491 |
|
| 2005 |
Ma S, Lu P, Lu L, Hou H, Wei J, He Q, Gu Z, Jiang X, Jin X. What can a metal catalyst do with allenes? One-step formation of steroid scaffolds from readily available starting materials. Angewandte Chemie (International Ed. in English). 44: 5275-8. PMID 16035021 DOI: 10.1002/Anie.200501350 |
0.628 |
|
| 2005 |
Ma S, Wu B, Jiang X. PdCl2-catalyzed efficient transformation of propargylic amines to (E)-alpha-chloroalkylidene-beta-lactams. The Journal of Organic Chemistry. 70: 2588-93. PMID 15787547 DOI: 10.1021/Jo0480996 |
0.429 |
|
| 2005 |
Ma S, Wu B, Jiang X, Zhao S. Studies on Pd(II)-catalyzed synthesis of (Z)-alpha-haloalkylidene-beta-lactones from cyclocarbonylation of 2-alkynols and the subsequent coupling reactions. The Journal of Organic Chemistry. 70: 2568-75. PMID 15787544 DOI: 10.1021/Jo0480038 |
0.419 |
|
| 2005 |
Jiang X, Shen M, Tang Y, Li C. Chemoselective monobromination of alkanes promoted by unactivated MnO 2 Tetrahedron Letters. 46: 487-489. DOI: 10.1016/J.Tetlet.2004.11.113 |
0.315 |
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