Enantio‐and diastereoselective Michael addition reactions of unmodified aldehydes and ketones with nitroolefins catalyzed by a pyrrolidine sulfonamide

J Wang, H Li, B Lou, L Zu, H Guo… - Chemistry–A European …, 2006 - Wiley Online Library
Chiral (S)‐pyrrolidine trifluoromethanesulfonamide has been shown to serve as an effective
catalyst for direct Michael addition reactions of aldehydes and ketones with nitroolefins. A …
被引用次数：255 相关文章

Enantio‐and Diastereoselective Michael Addition Reactions of Unmodified Aldehydes and Ketones with Nitroolefins Catalyzed by a Pyrrolidine Sulfonamide

J Wang, H Li, B Lou, L Zu, H Guo, W Wang - Chemistry–A European …, 2006 - cir.nii.ac.jp
抄録< jats: title> Abstract</jats: title>< jats: p> Chiral (< jats: italic> S</jats: italic>)‐pyrrolidine
trifluoromethanesulfonamide has been shown to serve as an effective catalyst for direct …

Enantio-and diastereoselective michael addition reactions of unmodified aldehydes and ketones with nitroolefins catalyzed by a pyrrolidine sulfonamide

J Wang, H Li, B Lou, L Zu, H Guo… - Chemistry-A European …, 2006 - pure.lib.cgu.edu.tw
摘要Chiral (S)-pyrrolidine trifluoromethanesulfonamide has been shown to serve as an
effective catalyst for direct Michael addition reactions of aldehydes and ketones with …

Enantio-and diastereoselective Michael addition reactions of unmodified aldehydes and ketones with nitroolefins catalyzed by a pyrrolidine sulfonamide.

J Wang, H Li, B Lou, L Zu, H Guo… - Chemistry (Weinheim an …, 2006 - europepmc.org
Chiral (S)-pyrrolidine trifluoromethanesulfonamide has been shown to serve as an effective
catalyst for direct Michael addition reactions of aldehydes and ketones with nitroolefins. A …

Enantio-and diastereoselective Michael addition reactions of unmodified aldehydes and ketones with nitroolefins catalyzed by a pyrrolidine sulfonamide

J Wang, H Li, B Lou, L Zu, H Guo… - … (Weinheim an der …, 2006 - pubmed.ncbi.nlm.nih.gov
Chiral (S)-pyrrolidine trifluoromethanesulfonamide has been shown to serve as an effective
catalyst for direct Michael addition reactions of aldehydes and ketones with nitroolefins. A …
[PDF] academia.edu

[PDF][PDF] Enantio-and Diastereoselective Michael Addition Reactions of Unmodified Aldehydes and Ketones with Nitroolefins Catalyzed by a Pyrrolidine Sulfonamide

J Wang, H Li, B Lou, L Zu, H Guo, W Wang - academia.edu
Chiral (S)-pyrrolidine trifluoromethanesulfonamide has been shown to serve as an effective
catalyst for direct Michael addition reactions of aldehydes and ketones with nitroolefins. A …

Enantio-and diastereoselective michael addition reactions of unmodified aldehydes and ketones with nitroolefins catalyzed by a pyrrolidine sulfonamide

J Wang, H Li, B Lou, L Zu, H Guo… - Chemistry-A European …, 2006 - pure.lib.cgu.edu.tw
Chiral (S)-pyrrolidine trifluoromethanesulfonamide has been shown to serve as an effective
catalyst for direct Michael addition reactions of aldehydes and ketones with nitroolefins. A …

[引用][C] Enantio‐and Diastereoselective Michael Addition Reactions of Unmodified Aldehydes and Ketones with Nitroolefins Catalyzed by a Pyrrolidine Sulfonamide.

J Wang, H Li, B Lou, L Zu, H Guo, W Wang - ChemInform, 2006 - Wiley Online Library