Enantioselective synthesis of α-perfluoroalkylated prolines, their 6,7-membered homologues and derivatives-Reference-Cited by-同舟云学术

Enantioselective synthesis of α-perfluoroalkylated prolines, their 6,7-membered homologues and derivatives

Published:2018 Issue:38 Volume:16 Page:7004-7011
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Voznesenskaia Natalia G.¹²³⁴,Shmatova Olga I.¹²³⁴,Khrustalev Victor N.⁵⁶⁴⁷⁸,Nenajdenko Valentine G.¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. Lomonosov Moscow State University

3. Moscow

4. Russia

5. Peoples’ Friendship University of Russia

6. 117198 Moscow

7. National Research Center “Kurchatov Institute”

8. Moscow 123182

Abstract

The highly enantioselective Strecker reaction with alpha-perfluoroalkylated cyclic ketimines was reported. The corresponding asymmetric cyclic nitriles are a useful tool for obtaining amino acids and their derivatives.

Funder

Russian Foundation for Basic Research

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB01223G

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