Pyrrolo[1,4]diazepines, via thermolyse of carbonylazides, and [3,2,2]cyclazines, via Diels-Alder reaction of [f]indolizines, annelated to [1]benzothiophene-Reference-Cited by-同舟云学术

Pyrrolo[1,4]diazepines, via thermolyse of carbonylazides, and [3,2,2]cyclazines, via Diels-Alder reaction of [f]indolizines, annelated to [1]benzothiophene

Published:1996-10 Issue:43 Volume:52 Page:13547-13556
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Ohier Philippe,Daïch Adam,Decroix Bernard

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference19 articles.

1. O-Debenzylation of a Pyrrolo[2,1-c][1,4]benzodiazepine in the Presence of a Carbinolamine Functionality: Synthesis of DC-81

2. Thienoquinolizidinones. Synthesis and rearrangement into new piperidino[1,2-a][1,3] or [1,4]diazepinones fused to a thiophene ring

3. Diazepines and naphthyridines from the rearrangement of thienoindolizidinone oximes

4. “Tert-amino effect” in heterocyclic synthesis. Synthesis of thieno[3,2-e]indolizines and thieno[2,3-c]quinolizines

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