Synthesis and thermal reactivity of thiazolo[3,4-a]benzimidazole-2,2-dioxides: approach to 1H-benzo[d]imidazoles via novel benzo-2,5-diazafulvenium methides-Reference-Cited by-同舟云学术

Synthesis and thermal reactivity of thiazolo[3,4-a]benzimidazole-2,2-dioxides: approach to 1H-benzo[d]imidazoles via novel benzo-2,5-diazafulvenium methides

Published:2015-06 Issue:24 Volume:71 Page:4227-4235
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Soares Maria I.L.^ORCID,Pinho e Melo Teresa M.V.D.^ORCID

Funder

Fundação para a Ciência e a Tecnologia

Portuguese Agency for Scientific Research

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference25 articles.

1. N-Vinyl- and C-Vinylpyrroles from Azafulvenium Methides. Flash Vacuum Pyrolysis Route to 5-Oxo-5H-pyrrolizines and 1-Azabenzo[f]azulenes

2. Chemistry of Diazafulvenium Methides in the Synthesis of Functionalized Pyrazoles

3. 1-Methyl-5-(trifluoromethyl)azafulvenium Methide, an Intermediate That Undergoes Reaction through “Unusual”cis-exo-1,3- andtrans-exo-1,7-Cycloadditions

4. Pericyclic Reactions of Azafulvenium Methides Bearing Internal Dipolarophiles - Synthesis of Chromene and Chromane Derivatives

5. Thiazolo[3,4-b]indazole-2,2-dioxides as Masked Extended Dipoles: Pericyclic Reactions of Benzodiazafulvenium Methides

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