Phosphine-catalyzed γ-addition of nitroacetates to allenoates for enantioselective creation of α,α-disubstituted α-amino acid precursors-Reference-Cited by-同舟云学术

Phosphine-catalyzed γ-addition of nitroacetates to allenoates for enantioselective creation of α,α-disubstituted α-amino acid precursors

Published:2021 Issue:21 Volume:8 Page:6114-6118
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Li Kaizhi¹,Lu Yixin²³^ORCID

Affiliation:

1. Biophamaceutical Research Institute, West China Hospital, Sichuan University, Chengdu 610041, China

2. Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore 117543

3. Joint School of National University of Singapore and Tianjin University, International Campus of Tianjin University, Binhai New City, Fuzhou, Fujian, 350207, China

Abstract

Enantioselective γ-addition of readily available α-substituted nitroacetates to allenoates has been achieved.

Funder

Faculty of Science, National University of Singapore

National Research Foundation Singapore

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/QO/D1QO01016F

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