The stereospecific preparation of two perfluoro-1,3-butadiene synthons; (E)-1-trimethylsilyl-1,2,3,4,4-pentafluoro-1,3-butadiene and (E)-1-tributylstannyl-1,2,3,4,4-pentafluoro-1,3-butadiene-Reference-Cited by-同舟云学术

The stereospecific preparation of two perfluoro-1,3-butadiene synthons; (E)-1-trimethylsilyl-1,2,3,4,4-pentafluoro-1,3-butadiene and (E)-1-tributylstannyl-1,2,3,4,4-pentafluoro-1,3-butadiene

Published:2003-01 Issue:1 Volume:119 Page:21-26
ISSN:0022-1139
Container-title:Journal of Fluorine Chemistry
language:en
Short-container-title:Journal of Fluorine Chemistry

Author:

Lim Chongsoo,Burton Donald J.,Wesolowski Craig A.

Publisher

Elsevier BV

Subject

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

Reference33 articles.

1. The stereospecific preparation of F-alkenyl cadmium reagents directly from F-alkenyl iodides and bromides and cadmium metal

2. The stereospecific preparation of fluorinated vinyl zinc reagents from polyfluorinated vinyl iodides or bromides and zinc metal

3. Palladium catalyzed coupling of F-cinyl zinc reagents with aryl iodides. An improved synthesis of α,β,β-trifluorostyrenes and the stereospecific preparation of 1-phenyl-F-propenes

4. Palladium-catalyzed cross-coupling of perfluoroalkenylzinc reagents with aryl iodides. A new, simple synthesis of .alpha.,.beta.,.beta.-trifluorostyrenes and the stereoselective preparation of 1-arylperfluoropropenes

5. A remarkable room temperature preparation of the trifluorovinylzinc reagent from HFC-134a. A cost-effective, high yield synthesis of α,β,β-trifluorostyrenes

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