Regio- and Stereocontrolled Stannylmetallation of 3,3-diethoxy-prop-1-yne and 4,4-diethoxy-but-1-yne : An efficient access to the corresponding vinyltins with fixed configurations-Reference-Cited by-同舟云学术

Regio- and Stereocontrolled Stannylmetallation of 3,3-diethoxy-prop-1-yne and 4,4-diethoxy-but-1-yne : An efficient access to the corresponding vinyltins with fixed configurations

Published:1991-10 Issue:44 Volume:32 Page:6333-6336
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Beaudet Isabelle,Parrain Jean-Luc,Quintard Jean-Paul

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference20 articles.

1. 1-Tributylstannyl-3,3-diethoxyprop-1 -ene as a d3acrolein equivalent

2. An efficient access to homoallyl and homocinnamyl skeletons using 1-tributylstannyl-4,4-diethoxy-but-1-ene

3. Palladium- and molybdenum-catalyzed hydrostannation of alkynes. A novel access to regio- and stereodefined vinylstannanes

4. Stereospecific synthesis of vinylstannanes using triphenylstannycopper(I) species. preparation of the cis-isomer of the presumed sex attractant of acanthoscelides obtectus.

5. Regio- and stereo-selective synthesis of vinylstannanes. Transition-metal catalyzed stannylmetalation of acetylenes and conversion of enol triflates and vinyl iodides into vinylstannanes

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