An experimental and theoretical study on the regioselective synthesis of a new class of spiropyrrolothiazoles with quinoxaline motifs via a 1,3-dipolar cycloaddition reaction. An evaluation of DFT methods-Reference-Cited by-同舟云学术

An experimental and theoretical study on the regioselective synthesis of a new class of spiropyrrolothiazoles with quinoxaline motifs via a 1,3-dipolar cycloaddition reaction. An evaluation of DFT methods

Published:2015 Issue:93 Volume:5 Page:76368-76376
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Hamzehloueian Mahshid¹²³⁴⁵,Sarrafi Yaghoub⁶⁷⁸⁹⁵,Aghaei Zahra⁶⁷⁸⁹⁵

Affiliation:

1. Department of Chemistry

2. Jouybar Branch

3. Islamic Azad University

4. Jouybar

5. Iran

6. Department of Organic Chemistry

7. Faculty of Chemistry

8. University of Mazandaran

9. 47416 Babolsar

Abstract

Evaluation of B3LYP/6-31G(d,p), wB97xD/6-31G(d,p) and M06-2X/6-31G(d,p) methods revealed the importance of π/π interactions in regio- and stereoselectivity of cycloaddition reactions.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA14071D

Reference103 articles.

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2. Katalytische enantioselektive 1,3-dipolare Cycloaddition von Azomethinyliden und Alkenen: der direkte Weg zu enantiomerenangereicherten mehrfach substituierten Prolinderivaten

3. K. V. Gothelf , in Cycloaddition Reactions in Organic Synthesis, ed. S. Kobayashi and K. A. Jørgensen, Wiley-VCH, Weinheim, 2002, pp. 211–247

4. Asymmetric 1,3-Dipolar Cycloaddition Reactions

5. An expedient approach for the synthesis of dispiropyrrolidine bisoxindoles, spiropyrrolidine oxindoles and spiroindane-1,3-diones through 1,3-dipolar cycloaddition reactions

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