Facile reduction of acid chlorides into aldehydes using hypervalent silicon hydrides.-Reference-Cited by-同舟云学术

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Facile reduction of acid chlorides into aldehydes using hypervalent silicon hydrides.

Published:1988-01 Issue:11 Volume:29 Page:1271-1274
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Corriu R.J.P.,Lanneau G.F.,Perrot M.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference24 articles.

1. STUDIES IN SILICO-ORGANIC COMPOUNDS. X. THE CHEMICAL PROPERTIES OF TRISUBSTITUTED SILANES1,2

2. Reductions with organosilicon hydrides. II. Preparation of aldehydes from acyl chlorides

3. The interaction of acyl halides and organosilicon hydrides catalysed by platinum and rhodium complexes. A new route to ketones

4. Palladium-catalyzed reaction of tributyltin hydride with acyl chlorides. A mild, selective, and general route to aldehydes

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1. Partial reductions of carboxylic acids and their derivatives to aldehydes;Organic Chemistry Frontiers;2022

2. Metal-free selective reduction of acid chlorides to aldehydes using 1-hydrosilatrane;Journal of Organometallic Chemistry;2021-12

3. Synthesis of Phthalic Aldehyde and Its Diacetals;Russian Journal of General Chemistry;2019-11

4. New methods to synthesize phthalaldehyde and its diacetals;Russian Chemical Bulletin;2019-10

5. Spontaneous Hydrosilylation of Substituted C=N Imines;European Journal of Inorganic Chemistry;2019-07-18

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