Rearrangement studies on 1-tetralylidenecyanothioacetamide: A different novel synthetic routes to strong fluorescent phenanthridine and phenanthrene analogues-Reference-Cited by-同舟云学术

Rearrangement studies on 1-tetralylidenecyanothioacetamide: A different novel synthetic routes to strong fluorescent phenanthridine and phenanthrene analogues

Published:1995-03 Issue:11 Volume:51 Page:3345-3350
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Elgemeie Galal E.H.,Fathy Nahed M.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference8 articles.

1. Nitriles in Heterocyclic Synthesis: Novel Synthesis of Pyrido[2,1-b]benzothiazoles, Pyrimido[6,1-b]benzothiazoles and Pyrazolo[4,3-c]pyridazine Derivatives

2. α,β-Unsaturated Nitriles in Heterocyclic Synthesis. Novel Synthesis of Pyridines and Thieno[2,3-b]pyridine Derivatives

3. Reaction of (Cyano)thioacetamide with Arylhydrazones ofβ-Diketones: Novel Synthesis of 2(1H)-Pyridinethiones, Thieno[2,3-b]pyridines, and Pyrazolo[3,4-b]pyridines

4. A convenient synthesis of 5-deaza nonclassical antifolates: Reaction of cyanothioacetamide with sodium salts of 2-(hydroxymethylene)-1-cycloalkanones

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