1-Aza-1′,3′-Diaza-3,3′-Sigmatropic Rearrangements — A Convenient Synthesis of Benzimidazole Derivatives-Reference-Cited by-同舟云学术

1-Aza-1′,3′-Diaza-3,3′-Sigmatropic Rearrangements — A Convenient Synthesis of Benzimidazole Derivatives

Published:1997-04 Issue:17 Volume:38 Page:3115-3118
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Teresa M,Carvalho V.L,Lobo* Ana M,Branco Paula S,Prabhakar* Sundaresan

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference13 articles.

1. For a review on the application of hetero-Cope rearrangements in organic synthesis, see: Blechert, S. Synthesis, 1989, 71–82.

2. The mechanism of the pellizzari transformation of α-cyanophenylhydrazine

3. Supplied by Aldrich Chem. Co (Spain).

4. For the preparation, using ClCN, the instability and reactivity of 1-phenyl-2-cyanohydrazine, see: Pellizzari, G; Tivoli, D. Gazz. Chim. Ital., 1892, 22, 226–236; Pellizzari, G. Gazz. Chim. Ital., 1910, 41, 54–59.

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