Hrydroxyl-directed iodoetherifications of allylic alcohols. Synthesis of (±)-citreoviral.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Iodine-mediated ring-closing iodoamination with concomitant N-debenzylation for the asymmetric synthesis of polyhydroxylated pyrrolidines;Tetrahedron: Asymmetry;2009-05
2. Development of Enolate Chemistry and Total Syntheses of Bioact ive Natural Products;Journal of Synthetic Organic Chemistry, Japan;2009
3. Pronounced Electronic Effect of Allylic Amino Groups on the π-Facial Stereoselectivity and Reactivity of the Iodoetherification of N-Substituted 3-Amino-4-penten-1-ols;Liebigs Annalen;2006-01-25
4. Highly Efficient Total Synthesis of (+)-Citreoviral;Angewandte Chemie International Edition;2004-06-14
5. Strategic Use of Pinacol-Terminated Prins Cyclizations in Target-Oriented Total Synthesis;The Journal of Organic Chemistry;2003-09-01
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