Strategies toward the Difunctionalizations of Enamide Derivatives for Synthesizing α,β-Substituted Amines-Reference-Cited by-同舟云学术

Strategies toward the Difunctionalizations of Enamide Derivatives for Synthesizing α,β-Substituted Amines

Published:2022-11-01 Issue:22 Volume:55 Page:3265-3283
ISSN:0001-4842
Container-title:Accounts of Chemical Research
language:en
Short-container-title:Acc. Chem. Res.

Author:

Bouchet Damien¹,Varlet Thomas¹,Masson Géraldine¹²^ORCID

Affiliation:

1. Institut de Chimie des Substances Naturelles, Université Paris-Saclay, ICSN-CNRS UPR 2301, 1 avenue de la Terasse, Gif-sur-Yvette 91198 Cedex, France

2. HitCat, Seqens-CNRS joint laboratory, Seqens’Lab, 8 Rue de Rouen, Porcheville 78440, France

Funder

Universit? Paris-Saclay

Centre National de la Recherche Scientifique

Institut de Chimie des Substances Naturelles

Publisher

American Chemical Society (ACS)

Subject

General Medicine,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.accounts.2c00540

Reference78 articles.

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2. Highly Enantioselective Electrophilic α-Bromination of Enecarbamates: Chiral Phosphoric Acid and Calcium Phosphate Salt Catalysts

3. Cerium(IV) Ammonium Nitrate Mediated Three-Component α-Allylation of Imine Surrogates

4. Preparation of Chiral Photosensitive Organocatalysts and Their Application for the Enantioselective Synthesis of 1,2-Diamines

5. Enamides and Enecarbamates as Nucleophiles in Stereoselective C–C and C–N Bond-Forming Reactions

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