Sodium borodeuteride reduction ofN,N-dimethyl-α-chloro-α,α-diphenyl-acetamide and the mechanism of the “normal” reaction of α-chloro-α,α-diphenylacetamides with nucleophiles-Reference-Cited by-同舟云学术

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Sodium borodeuteride reduction ofN,N-dimethyl-α-chloro-α,α-diphenyl-acetamide and the mechanism of the “normal” reaction of α-chloro-α,α-diphenylacetamides with nucleophiles

Published:1975-01 Issue:2 Volume:16 Page:93-96
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Simig Gy.,Lempert K.,Tama´s J.,Miklo´s P.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference5 articles.

1. A novel displacement reaction on α-chlorodiphenylacetamides

2. Über die anomale substitutionsreaktion von α-chlor-α,α-diphenyl-acetamiden mit kalium-phenylcyanamid

3. Gy. Simig and K. Lempert, Tetrahedron, accepted for publication

4. Some Novel Eliminations of Neutral Fragments from Ions in Mass Spectrometry

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. On the mechanism of formation of dimeric and reduced products from an α-halo amide with sodium methoxide;Tetrahedron;1978-01

2. Anomalous substitutions and reductive dehalogenations of α,α-diaryl-α-halogeno- n,n-dimethylacetamides by methoxide;Tetrahedron Letters;1977-01

3. ChemInform Abstract: SODIUM BORODEUTERIDE REDUCTION OF N,N-DIMETHYL-ALPHA-CHLORO-ALPHA,ALPHA-DIPHENYL-ACETAMIDE AND THE MECHANISM OF THE ′NORMAL′ REACTION OF ALPHA-CHLORO-ALPHA,ALPHA-DIPHENYLACETAMIDES WITH NUCLEOPHILES;Chemischer Informationsdienst;1975-04-15

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