Quantum Chemical Analysis and Experimental Study of the Cycloaddition Reaction between Aminoacetylenes and 6-Nitroindolizines. NMR and ab Initio Evidence for the [4+2] Adduct Formation-Reference-Cited by-同舟云学术

Quantum Chemical Analysis and Experimental Study of the Cycloaddition Reaction between Aminoacetylenes and 6-Nitroindolizines. NMR and ab Initio Evidence for the [4+2] Adduct Formation

Published:1999-11-20 Issue:25 Volume:64 Page:9057-9062
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Babaev Eugene V.¹,Simonyan Vahan V.¹,Pasichnichenko Konstantin Yu.¹,Nosova Valentina M.¹,Kisin Alexander V.¹,Jug Karl¹

Affiliation:

1. Chemical Department, Moscow State University, Moscow 119899, Russia, Theoretische Chemie, Universität Hannover, Am Kleinen Felde 30, Hannover D 30167, Germany, and State Research Institute of Chemistry and Technology of Organoelement Compounds, Moscow 111123, Sh Enthuziastov 38, Russia

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo990841s

Reference29 articles.

1. The Formation of Cycl[3.2.2]azine Derivatives via the Reaction of Pyrrocoline with Dimethyl Acetylenedicarboxylate

2. Indolizine derivatives. IX. Preparation of 1-acylpyrrolo[2,1,5-cd]indolizinesviacycloaddition of 3-acyloxyindolizines to active ethylenes and acetylenes

3. PERIPHERAL CONJUGATE SYSTEMS 1. CYCLOADDITION OF INDOLIZINE TO ELECTRON-DEFICIENT OLEFIN

4. CYCLOADDITION REACTION OF 3-CYANOINDOLIZINES WITH DIMETHYL ACETYLENEDICARBOXYLATE —FORMATION OF CYCL[3.2.2]AZINES AND 1:2 ADDUCTS

5. Aromaticity-Based Theory of Pericyclic Reactions

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