Year |
Citation |
Score |
2023 |
Xiao Y, Xu TT, Zhou JL, Wu F, Tang L, Liu RY, Wu WB, Feng JJ. Photochemical α-selective radical ring-opening reactions of 1,3-disubstituted acyl bicyclobutanes with alkyl halides: modular access to functionalized cyclobutenes. Chemical Science. 14: 13060-13066. PMID 38023515 DOI: 10.1039/d3sc04457b |
0.394 |
|
2023 |
Tang L, Xiao Y, Wu F, Zhou JL, Xu TT, Feng JJ. Silver-Catalyzed Dearomative [2π+2σ] Cycloadditions of Indoles with Bicyclobutanes: Access to Indoline Fused Bicyclo[2.1.1]hexanes. Angewandte Chemie (International Ed. in English). e202310066. PMID 37822277 DOI: 10.1002/anie.202310066 |
0.331 |
|
2023 |
Tang L, Huang QN, Wu F, Xiao Y, Zhou JL, Xu TT, Wu WB, Qu S, Feng JJ. C(sp)-H cyclobutylation of hydroxyarenes enabled by silver-π-acid catalysis: diastereocontrolled synthesis of 1,3-difunctionalized cyclobutanes. Chemical Science. 14: 9696-9703. PMID 37736637 DOI: 10.1039/d3sc03258b |
0.362 |
|
2023 |
Xiao Y, Tang L, Xu TT, Sheng JY, Zhou Z, Yue L, Wang G, Oestreich M, Feng JJ. Atom-economic and stereoselective catalytic synthesis of fully substituted enol esters/carbonates of amides in acyclic systems enabled by boron Lewis acid catalysis. Chemical Science. 14: 5608-5618. PMID 37265723 DOI: 10.1039/d3sc01394d |
0.611 |
|
2022 |
Xiao Y, Tang L, Xu TT, Feng JJ. Boron Lewis Acid Catalyzed Intermolecular -Hydroarylation of Ynamides with Hydroxyarenes. Organic Letters. PMID 35389667 DOI: 10.1021/acs.orglett.2c00574 |
0.375 |
|
2020 |
Feng JJ, Mao W, Zhang L, Oestreich M. Activation of the Si-B interelement bond related to catalysis. Chemical Society Reviews. PMID 33325936 DOI: 10.1039/d0cs00965b |
0.573 |
|
2019 |
Feng JJ, Xu Y, Oestreich M. Ligand-controlled diastereodivergent, enantio- and regioselective copper-catalyzed hydroxyalkylboration of 1,3-dienes with ketones. Chemical Science. 10: 9679-9683. PMID 32015801 DOI: 10.1039/C9Sc03531A |
0.551 |
|
2019 |
Feng JJ, Oestreich M. Tertiary α-Silyl Alcohols by Diastereoselective Coupling of 1,3-Dienes and Acylsilanes Initiated by Enantioselective Copper-Catalyzed Borylation. Angewandte Chemie (International Ed. in English). PMID 30947388 DOI: 10.1002/Anie.201903174 |
0.559 |
|
2019 |
Feng J, Oestreich M. Tertiäre α‐Silylalkohole mittels diastereoselektiver Kupplung von 1,3‐Dienen und Acylsilanen, eingeleitet durch enantioselektive kupferkatalysierte Borylierung Angewandte Chemie. 131: 8295-8299. DOI: 10.1002/Ange.201903174 |
0.371 |
|
2018 |
Feng JJ, Oestreich M. Copper-Catalyzed Silylation of C(sp)-H Bonds Adjacent to Amide Nitrogen Atoms. Organic Letters. PMID 29956941 DOI: 10.1021/Acs.Orglett.8B01698 |
0.529 |
|
2018 |
Lin TY, Wu HH, Feng JJ, Zhang J. Chirality Transfer in Rhodium(I)-Catalyzed [3 + 2]-Cycloaddition of Vinyl Aziridines and Oxime Ethers: Atom-Economical Synthesis of Chiral Imidazolidines. Organic Letters. PMID 29863882 DOI: 10.1021/Acs.Orglett.8B01378 |
0.529 |
|
2018 |
Zhu CZ, Feng JJ, Zhang J. Divergent synthesis of functionalized pyrrolidines and γ-amino ketones via rhodium-catalyzed switchable reactions of vinyl aziridines and silyl enol ethers. Chemical Communications (Cambridge, England). PMID 29457188 DOI: 10.1039/C8Cc00279G |
0.486 |
|
2017 |
Lin TY, Wu HH, Feng JJ, Zhang J. Divergent Access to Functionalized Pyrrolidines and Pyrrolines via Iridium-Catalyzed Domino-Ring-Opening Cyclization of Vinyl Aziridines with β-Ketocarbonyls. Organic Letters. PMID 29164890 DOI: 10.1021/Acs.Orglett.7B03232 |
0.453 |
|
2017 |
Lin TY, Wu HH, Feng JJ, Zhang J. Transfer of Chirality in the Rhodium-Catalyzed Chemoselective and Regioselective Allylic Alkylation of Hydroxyarenes with Vinyl Aziridines. Organic Letters. PMID 28530815 DOI: 10.1021/Acs.Orglett.7B01136 |
0.505 |
|
2017 |
Zhu CZ, Feng JJ, Zhang J. Rhodium-catalyzed intermolecular [3+3] cycloaddition of vinyl aziridines with C,N-cyclic azomethine imines: stereospecific synthesis of chiral fused tricyclic 1,2,4-hexahydrotriazines. Chemical Communications (Cambridge, England). PMID 28401219 DOI: 10.1039/C7Cc02078C |
0.492 |
|
2017 |
Zhu C, Feng J, Zhang J. Rhodium(I)-Catalyzed Stereospecific [3+2] Cycloadditions of Vinylaziridines and Ynamides Chinese Journal of Organic Chemistry. 37: 1165. DOI: 10.6023/Cjoc201701043 |
0.504 |
|
2017 |
Lin T, Wu H, Feng J, Zhang J. Design and Enantioselective Synthesis of β-Vinyl Tryptamine Building Blocks for Construction of Privileged Chiral Indole Scaffolds Acs Catalysis. 7: 4047-4052. DOI: 10.1021/Acscatal.7B00870 |
0.471 |
|
2017 |
Feng J, Zhang J. Rhodium-Catalyzed Stereoselective Intramolecular Tandem Reaction of Vinyloxiranes with Alkynes: Atom- and Step-Economical Synthesis of Multifunctional Mono-, Bi-, and Tricyclic Compounds Acs Catalysis. 7: 1533-1542. DOI: 10.1021/Acscatal.6B03399 |
0.517 |
|
2016 |
Zhu CZ, Feng JJ, Zhang J. Rhodium(I)-Catalyzed Intermolecular Aza-[4+3] Cycloaddition of Vinyl Aziridines and Dienes: Atom-Economical Synthesis of Enantiomerically Enriched Functionalized Azepines. Angewandte Chemie (International Ed. in English). PMID 27966804 DOI: 10.1002/Anie.201609608 |
0.53 |
|
2016 |
Lin TY, Zhu CZ, Zhang P, Wang Y, Wu HH, Feng JJ, Zhang J. Regiodivergent Intermolecular [3+2] Cycloadditions of Vinyl Aziridines and Allenes: Stereospecific Synthesis of Chiral Pyrrolidines. Angewandte Chemie (International Ed. in English). PMID 27485044 DOI: 10.1002/Anie.201605530 |
0.478 |
|
2016 |
Feng JJ, Lin TY, Zhu CZ, Wang H, Wu HH, Zhang J. The Divergent Synthesis of Nitrogen Heterocycles by Rhodium(I)-Catalyzed Intermolecular Cycloadditions of Vinyl Aziridines and Alkynes. Journal of the American Chemical Society. PMID 26859710 DOI: 10.1021/Jacs.6B00386 |
0.438 |
|
2016 |
Feng JJ, Zhang J. Synthesis of Unsaturated N-Heterocycles by Cycloadditions of Aziridines and Alkynes Acs Catalysis. 6: 6651-6661. DOI: 10.1021/Acscatal.6B02072 |
0.479 |
|
2016 |
Feng J, Zhang J. ChemInform Abstract: Synthesis of Unsaturated N-Heterocycles by Cycloadditions of Aziridines and Alkynes Cheminform. 47. DOI: 10.1002/CHIN.201649206 |
0.323 |
|
2015 |
Feng JJ, Lin TY, Wu HH, Zhang J. Modular Access to the Stereoisomers of Fused Bicyclic Azepines: Rhodium-Catalyzed Intramolecular Stereospecific Hetero-[5+2] Cycloaddition of Vinyl Aziridines and Alkenes. Angewandte Chemie (International Ed. in English). PMID 26555739 DOI: 10.1002/Anie.201509185 |
0.504 |
|
2015 |
Feng JJ, Lin TY, Wu HH, Zhang J. Transfer of chirality in the rhodium-catalyzed intramolecular formal hetero-[5 + 2] cycloaddition of vinyl aziridines and alkynes: stereoselective synthesis of fused azepine derivatives. Journal of the American Chemical Society. 137: 3787-90. PMID 25763476 DOI: 10.1021/Jacs.5B01305 |
0.525 |
|
2014 |
Chen Y, Feng J, Duan W. NHC–copper-catalyzed asymmetric 1,4-addition of diarylphosphines to α,β-unsaturated ketones Tetrahedron Letters. 55: 595-597. DOI: 10.1016/J.Tetlet.2013.10.158 |
0.422 |
|
2013 |
Feng J, Huang M, Lin Z, Duan W. ChemInform Abstract: Palladium-Catalyzed Asymmetric 1,4-Addition of Diarylphosphines to Nitroalkenes for the Synthesis of Chiral P,N-Compounds. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201316172 |
0.311 |
|
2012 |
Feng J, Huang M, Lin Z, Duan W. Palladium-Catalyzed Asymmetric 1,4-Addition of Diarylphosphines to Nitroalkenes for the Synthesis of Chiral P,N-Compounds Advanced Synthesis & Catalysis. 354: 3122-3126. DOI: 10.1002/Adsc.201200133 |
0.433 |
|
2011 |
Feng JJ, Zhang J. An atom-economic synthesis of bicyclo[3.1.0]hexanes by rhodium N-heterocyclic carbene-catalyzed diastereoselective tandem hetero-[5+2] cycloaddition/Claisen rearrangement reaction of vinylic oxiranes with alkynes. Journal of the American Chemical Society. 133: 7304-7. PMID 21524076 DOI: 10.1021/Ja2014604 |
0.509 |
|
2010 |
Feng JJ, Chen XF, Shi M, Duan WL. Palladium-catalyzed asymmetric addition of diarylphosphines to enones toward the synthesis of chiral phosphines. Journal of the American Chemical Society. 132: 5562-3. PMID 20359215 DOI: 10.1021/Ja100606V |
0.448 |
|
2008 |
Shen W, Wang L, Feng J, Tian H. Highly efficient synthesis of homoallylic alcohols and amines via allylation of aldehydes and imines catalyzed by ZrOCl2·8H2O in water Tetrahedron Letters. 49: 4047-4049. DOI: 10.1016/J.Tetlet.2008.04.084 |
0.378 |
|
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