Croncise organocatalytic route to protected (2S, 4R)-4-hydroxyornithine and(+)-pseudohygroline

TitleCroncise organocatalytic route to protected (2S, 4R)-4-hydroxyornithine and(+)-pseudohygroline
Publication TypeJournal Article
Year of Publication2014
AuthorsJha, V, Kumar, P
JournalSynlett
Volume25
Issue8
Pagination1089-1092
Date PublishedMAY
ISSN0936-5214
Keywordsaldehydes, Amination, Amino alcohols, cyclization, Enantioselectivity, Wittig reaction
Abstract

A practical, efficient, and organocatalytic approach to the synthesis of (2S,4R)-4-hydroxyornithine and (+)-pseudohygroline is reported using proline-catalyzed sequential alpha-aminoxylation/alpha-amination reaction and Horner-Wadsworth-Emmons olefination reaction of an aldehyde as the key step.

DOI10.1055/s-0033-1340977
Type of Journal (Indian or Foreign)

Foreign

Impact Factor (IF)

2.323

Divison category: 
Organic Chemistry