Organocatalytic route to the enantioselective synthesis of syn/ anti-α-hydrazino-γ-fluoro alcohols

TitleOrganocatalytic route to the enantioselective synthesis of syn/ anti-α-hydrazino-γ-fluoro alcohols
Publication TypeJournal Article
Year of Publication2024
AuthorsKhonde, NS, Said, MS, Danve, SS, Kumar, P
JournalTetrahedron Letters
Volume145
Pagination155179
Date PublishedJUL
Type of ArticleArticle
ISSN0040-4039
Keywordsalpha-Amination, alpha-Fluorination, diastereoselectivity, Enantioselectivity, HWE olefination, organocatalyst
Abstract

A general organocatalytic method has been developed for the asymmetric synthesis of alpha-hydrazino-gamma-fluoro alcohols, a precursor to syn/anti-1,3-fluoro amines. The strategy employs alpha-fluorination catalyzed by prolinederived catalyst, (S)-alpha,alpha-bis[3,5-bis(trifluoromethyl)phenyl]-2-pyrrolidinemetha nol trimethylsilyl ether followed by Horner-Wadsworth-Emmons (HWE) olefination of aldehydes, and proline-catalyzed alpha-amination as the key steps. The title compounds showed excellent diastereoselectivity (up to 99:1) and enantioselectivity (up to 99 %).

DOI10.1016/j.tetlet.2024.155179
Type of Journal (Indian or Foreign)

Foreign

Impact Factor (IF)

1.8

Divison category: 
Organic Chemistry
Database: 
Web of Science (WoS)

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