3-Iodopropenoylsylane: a Further Step in the Chemistry of Unsaturated Acylsilanes

DOI: 10.1016/S0040-4039(00)73055-3

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Tetrahedron Letters p. 2081 - 2082 (1994)

Update date:2022-08-10

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Authors:

Degl'Innocenti, Alessandro

Capperucci, Antonella

Bartoletti, Laura

Mordini, Alessandro

Reginato, Gianna

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Article abstract of DOI:10.1016/S0040-4039(00)73055-3

(E)-3-iodo propenoyltriphenylsilane 2 undergoes smooth coupling reactions with a variety of unsaturated organostannanes to afford polyunsaturated acylsilanes.

Full text of DOI:10.1016/S0040-4039(00)73055-3

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Article Doi

3-Iodopropenoylsylane: a Further Step in the Chemistry of Unsaturated Acylsilanes

DOI: 10.1016/S0040-4039(00)73055-3

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)73055-3

Full text of DOI:10.1016/S0040-4039(00)73055-3

Products guided by the article

R&D Labs maybe for 141097-43-0

Relevant to this article

BENZOPHENONE-SENSITIZED PHOTOLYSIS OF THE AZOALKANE DIAZABICYCLO(2.2.1)HEPT-2-ENE (DBH) : TRAPPING OF THE 1,3-CYCLOPENTADIYL TRIPLET DIRADICAL BY A NITROXIDE.

Understanding and Interrupting the Fischer Azaindolization Reaction

The facile oxidative coupling of a hindered phenol, 2,6-di-t-butylphenol, driven by N,N′-bis(ethoxy-carbonyl)-1,4-benzoquinone diimine; The reaction pattern traced by 1H NMR spectroscopy

Self-assembled vesicle and rod-like aggregates of functionalized perylene diimide: Reaction-based near-IR intracellular fluorescent probe for selective detection of palladium

The facile oxidative coupling of a hindered phenol, 2,6-di-t-butylphenol, driven by N,N′-bis(ethoxy-carbonyl)-1,4-benzoquinone diimine; The reaction pattern traced by ¹H NMR spectroscopy