Hydroxylamine-alkyne cyclisations. Synthesis of the seven-membered lactam structure proposed for (±)-acacialactam
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. Fox, M.E.; Holmes, A.B.; Forbes, I.T.; Thompson, M. preceding Letter.
2. (+)-Acacialactam, a new seven-membered lactam from the seeds of Acacia concinna.
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1. Reverse Cope Elimination of Hydroxylamines and Alkenes or Alkynes: Theoretical Investigation of Tether Length and Substituent Effects;Journal of the American Chemical Society;2012-01-17
2. ChemInform Abstract: Hydroxylamine - Alkyne Cyclizations. Synthesis of the Seven-Membered Lactam Structure Proposed for (.+-.)-Acacialactam.;ChemInform;2010-08-20
3. Intermolecular Cope-Type Hydroamination of Alkenes and Alkynes using Hydroxylamines;Journal of the American Chemical Society;2008-12-31
4. Hydroxylamine;Encyclopedia of Reagents for Organic Synthesis;2006-09-15
5. The reverse Cope cyclisation: a classical reaction goes backwards;Tetrahedron;2004-01
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