Improved Stereoselectivity in Intramolecular SN2′ Cyclization through Use of Mechanistic Principles
Abstract
Valine and alanine were converted into the corresponding α-hydroxy-β-amino acids through intramolecular SN2′ cyclization. The novel cyclization protocol relied upon the use of N-benzyl-protected carbamates derived from α-amino...
Paper Details
Title
Improved Stereoselectivity in Intramolecular SN2′ Cyclization through Use of Mechanistic Principles
Published Date
Jan 1, 2007
Journal
Volume
2007
Issue
2
Pages
209 - 214
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