Stereochemistry modulates the catalytic hydrogenolysis of nitrile-substituted cyclopropanes-Reference-Cited by-同舟云学术

Stereochemistry modulates the catalytic hydrogenolysis of nitrile-substituted cyclopropanes

Published:2012-09 Issue:35 Volume:68 Page:7187-7195
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

González-Juárez Daphne E.,García-Vázquez J. Benjamín,Zúñiga-García Violeta,Trujillo-Serrato Joel J.,Suárez-Castillo Oscar R.,Joseph-Nathan Pedro,Morales-Ríos Martha S.

Funder

CONACYT grants

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference40 articles.

1. Design and synthesis of dipeptidyl nitriles as potent, selective, and reversible inhibitors of cathepsin C

2. Stereoselective synthesis of quaternary α-amino acids. Part 2: Cyclic compounds

3. Palladium-catalyzed domino Heck/cyanation: synthesis of 3-cyanomethyloxindoles and their conversion to spirooxoindoles

4. Trifluoromethanesulfonyl azide: an efficient reagent for the preparation of α-cyano-α-diazo carbonyls and an α-sulfonyl-α-diazo carbonyl

5. Natural Occurrence, Syntheses, and Applications of Cyclopropyl-Group-Containing α-Amino Acids. 2. 3,4- and 4,5-Methanoamino Acids

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