An efficient synthesis of (Z)-γ-fluoroallylphosphonates using a base-promoted deconjugation of (E)-γ-fluorovinylphosphonates, and its utility as fluoroolefin-containing building block-Reference-Cited by-同舟云学术

An efficient synthesis of (Z)-γ-fluoroallylphosphonates using a base-promoted deconjugation of (E)-γ-fluorovinylphosphonates, and its utility as fluoroolefin-containing building block

Published:2000-03 Issue:1-2 Volume:102 Page:189-197
ISSN:0022-1139
Container-title:Journal of Fluorine Chemistry
language:en
Short-container-title:Journal of Fluorine Chemistry

Author:

Hammond Gerald B.,deMendonca Daniel J.

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Environmental Chemistry,Biochemistry

Reference37 articles.

1. A Highly Selective Synthesis of a Chiral Gamma-amino Trisubstituted Z-Vinyl Ester.1

2. Synthesis of a fluorinated analog of the sex pheromone of the processionary moth thaumetopoea. pityocampa(denis and schiff.)

3. Synthesis of dienic fluorinated analogs of insect sex pheromones

4. A Convenient and Stereoselective Synthesis of (3Z,5Z)-5-Fluorotetrade Cadien-1-yl Acetate, A Fluorinated Analog of the sex Pheromone of the CarpenterwormPrionoxistus robiniae(Peck)

5. New geometric isomers of vitamin A and carotenoids. 6. Fluorinated rhodopsin analogs from 10-fluoro- and 14-fluororetinal

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