Publication
Title
Enantioselective synthesis of (-)-(6R,7S)-nitramine
Author
Abstract
The spirocyclic (-)-(6R,7S)-nitramine was prepared in a straightforward way from an appropriately substituted chiral alpha-allylaldimine precursor involving an electrophile-induced cyclization as the key step.
Language
English
Source (book)
Natural products in the new millennium : prospects and industrial applications : Meeting of the Phytochemical-Society-of-Europe, April 02-05, 2000, Fund Calouste Gulbenkian, Lisbon, Portugal
Publication
Dordrecht : Springer, 2002
ISBN
1-4020-1047-8
Volume/pages
47(2002), p. 407-413
ISI
000180547900040
UAntwerpen
Faculty/Department
Publication type
Subject
External links
Web of Science
Record
Identification
Creation 28.01.2013
Last edited 27.11.2017