Stereocontrolled Construction of Acyclic Quaternary Carbon Centers via α-Hydroxymethylation of α-Branched N-tert-Butanesulfinyl Ketimines
Author:
Affiliation:
1. School of Chemical Science and Technology, Yunnan University, Kunming, Yunnan 650091, People’s Republic of China
Funder
Yunnan University
National Natural Science Foundation of China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c03171
Reference52 articles.
1. Asymmetric Aldol Reaction with Formaldehyde: a Challenging Process
2. Catalytic enantioselective aldol reactions
3. Enantioselective synthesis of all-carbon quaternary stereogenic centers in acyclic systems
4. Catalytic enantioselective construction of vicinal quaternary carbon stereocenters
5. Synthesis of Enantioenriched Vicinal Tertiary and Quaternary Carbon Stereogenic Centers within an Acyclic Chain
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2. Stereodivergent conjugate reduction of α-substituted α,β-unsaturated N-sulfinyl ketimines: flexible access to challenging acyclic β,β-disubstituted enesulfinamides;Organic Chemistry Frontiers;2024
3. Stereoselective Construction of Vicinal Quaternary Stereocenters via the 1,6-Conjugate Addition of β,β-Disubstituted N-Sulfinyl Metalloenamines to Isatin-Derived para-Quinone Methides;Synthesis;2023-12-06
4. Stereoselective Construction of Acyclic β,β-Disubstituted Enesulfinamides via Conjugate Addition of Organocuprates to α-Substituted α,β-Unsaturated N-Sulfinyl Ketimines;Organic Letters;2023-07-17
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