Regio- and stereoselectivity in the cyclization of enolates derived from 4,5-, 5,6-, and 6,7-epoxy-1-phenyl-1-alkanones. Competition between C- and O-alkylation-Reference-Cited by-同舟云学术

Regio- and stereoselectivity in the cyclization of enolates derived from 4,5-, 5,6-, and 6,7-epoxy-1-phenyl-1-alkanones. Competition between C- and O-alkylation

Published:1999-04 Issue:18 Volume:55 Page:5853-5866
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Crotti Paolo,Di Bussolo Valeria,Favero Lucilla,Macchia Franco,Pineschi Mauro,Napolitano Elio

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

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4. Metal Salt-Catalyzed Addition of Lithium Enolates of Ketones to 1,2-Epoxides. An Efficient Route to α-Alkyl-γ-Hydroxy Ketones

5. Alternative total synthesis of (±)-β-santalene, (±)-epi-β-santalene, (±)-α-santalene, (±)-copacamphor and (±)-ylangocamphor

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