Ab Initio and Density Functional Calculations on the Pericyclic vs Pseudopericyclic Mode of Conjugated Nitrile Ylide 1,5-Electrocyclizations-Reference-Cited by-同舟云学术

Ab Initio and Density Functional Calculations on the Pericyclic vs Pseudopericyclic Mode of Conjugated Nitrile Ylide 1,5-Electrocyclizations

Published:1999-12-12 Issue:1 Volume:65 Page:47-53
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Fabian Walter M. F.¹,Kappe C. Oliver¹,Bakulev Vasiliy A.¹

Affiliation:

1. Institute of Organic Chemistry, Karl-Franzens University, Graz, Heinrichstr. 28, A-8010 Graz, Austria, and Department of Technology of Organic Synthesis, Urals State Technical University, Mira 19, 620002 Ekaterinburg, Russia

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo990997s

Reference71 articles.

1. 1.3‐Dipolare Cycloadditionen, 62. Benzonitril‐[4‐nitro‐benzylid] und seine Reaktionen mit CC‐Doppel‐ und CC‐Dreifachbindungen

2. 1,3-Dipolar Additions with Nitrile Ylides

3. Facile Synthesis of 2-Aryl- and 2-Heteroarylpyrroles fromN-Allylcarboxamides

4. Photochemical transformations of small ring heterocyclic systems. LXV. Intramolecular cycloaddition reactions of vinyl-substituted 2H-azirines

5. Photochemical transformations of small ring heterocyclic compounds. 71. Intramolecular reorganization of some unsaturated 2H-azirines

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