Regioselective electrophilic additions to 2-oxygenated-7-oxabicyclo[2.2.1]Hept-5-enes: A simple entry into the 4,7-dioxatricyclo[3.2.1.03,6]octaneskeleton-Reference-Cited by-同舟云学术

Regioselective electrophilic additions to 2-oxygenated-7-oxabicyclo[2.2.1]Hept-5-enes: A simple entry into the 4,7-dioxatricyclo[3.2.1.03,6]octaneskeleton

Published:1989 Issue:14 Volume:45 Page:4565-4578
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Arjona Odon,de la Pradilla Roberto Fernandez,Plumet★ Joaquin,Viso Alma

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference51 articles.

1. Five-membered heteroaromatic rings as intermediates in organic synthesis

2. Synthesis and pharmacological evaluation of 5,6-exo-epoxy-7-oxabicyclo[2.2.1]heptane derivatives

3. Synthesis of oxabicyclo[2.2.1]heptane prostanoids having thromboxane-like activity at sub-nanomolar concentrations

4. The ring opening metathesis polymerization of 7-oxabicyclo[2.2.1]hept-5-ene derivatives: a new acyclic polymeric ionophore

5. Synthetic Approach to the Ivermectin Bottom Half Using Internal Cycloadducts of N-Furfuryl Acrylamides: Functionality and Optical Activity

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