Aminolysis of sulfinamoyl-esters, -sulfonamides and -sulfones. Thiooxamate and thiourea formation via a sulfine intermediate. Thiophilic or carbophilic reaction?-Reference-Cited by-同舟云学术

Aminolysis of sulfinamoyl-esters, -sulfonamides and -sulfones. Thiooxamate and thiourea formation via a sulfine intermediate. Thiophilic or carbophilic reaction?

Published:1996-11 Issue:47 Volume:52 Page:14865-14876
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Baltas M.,Raouf-Benchekroun K.,De Blic A.,Cazaux L.,Tisnès P.,Gorrichon L.,Hussein K.,Barthelat J.-C.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference35 articles.

1. Enzymic Synthesis of Lignin Precursors Comparison of Cinnamoyl-CoA Reductase and Cinnamyl Alcohol: NADP+ Dehydrogenase from Spruce (Picea abies L.) and Soybean (Glycine max L.)

2. Molecular cloning and expression of a Eucalyptus gunnii cDNA clone encoding cinnamyl alcohol dehydrogenase

3. A molecular model for cinnamyl alcohol dehydrogenase, a plant aromatic alcohol dehydrogenase involved in lignification

4. Site-Directed Mutagenesis of a Serine Residue in Cinnamyl Alcohol Dehydrogenase, a Plant NADPH-Dependent Dehydrogenase, Affects the Specificity for the Coenzyme

5. A Convenient and Facile Synthesis of β-Aminosulfinyl-and β-Aminosulfonylalkanoic Esters from Metallated Esters andN-Sulfinylamines

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