Pseudopericyclic 1,5- versus Pericyclic 1,4- and 1,6-Electrocyclization in Electron-Poor 4-Aryl-2-azabuta-1,3-dienes: Indole Synthesis from 2H-Azirines and Diazo Compounds-Reference-Cited by-同舟云学术

Pseudopericyclic 1,5- versus Pericyclic 1,4- and 1,6-Electrocyclization in Electron-Poor 4-Aryl-2-azabuta-1,3-dienes: Indole Synthesis from 2H-Azirines and Diazo Compounds

Published:2014-12-09 Issue:1 Volume:80 Page:18-29
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Novikov Mikhail S.¹,Khlebnikov Alexander F.¹,Rostovskii Nikolai V.¹,Tcyrulnikov Sergei¹,Suhanova Anna A.¹,Zavyalov Kirill V.¹,Yufit Dmitry S.²

Affiliation:

1. Institute of Chemistry, Saint-Petersburg State University, Universitetskii pr. 26, 198504 St. Petersburg, Russia

2. Department of Chemistry, University of Durham, South Road, Durham DH1 3LE, U.K.

Funder

Russian Foundation for Basic Research

Saint Petersburg State University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo501051n

Reference49 articles.

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2. Recent advances in synthetic applications of azadienes

3. Aza-2-dienes-1,3. Partie 5. Préparation deN-aminoimidazoles, 3H-pyrroles, triazolo[1,2,4][1,5-a]pyrazines et imidazo[1,2-a]pyrazines

4. Iminophosphoranes: Useful Building Blocks for the Preparation of Nitrogen-Containing Heterocycles

5. Synthesis of 3-phosphorylated 2-aza-1,3-dienes from imines derived from bisphosphonates

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