Mechanistic studies of 1,3-dipolar cycloadditions of bicyclic thioisomünchnones with alkenes. A computational rationale focused on donor–acceptor interactions-Reference-Cited by-同舟云学术

Mechanistic studies of 1,3-dipolar cycloadditions of bicyclic thioisomünchnones with alkenes. A computational rationale focused on donor–acceptor interactions

Published:2018 Issue:18 Volume:16 Page:3438-3452
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

García de la Concepción Juan¹²³⁴⁵^ORCID,Ávalos Martín¹²³⁴⁵,Cintas Pedro¹²³⁴⁵^ORCID,Jiménez José L.¹²³⁴⁵,Light Mark E.⁶⁷⁸⁹^ORCID

Affiliation:

1. Departamento de Química Orgánica e Inorgánica

2. Facultad de Ciencias-UEX

3. IACYS-Unidad de Química Verde y Desarrollo Sostenible

4. E-06006 Badajoz

5. Spain

6. Department of Chemistry

7. University of Southampton

8. Southampton SO17 1BJ

9. UK

Abstract

Unlike monocyclic mesoionic dipoles, bicyclic thioisomünchnones provide high levels of regio- and stereoselection leading to heteroatom-rich polycycles.

Funder

European Regional Development Fund

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB00683K

Reference48 articles.

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4. Recent Advances of Catalytic Asymmetric 1,3-Dipolar Cycloadditions

5. Progress in 1,3-dipolar cycloadditions in the recent decade: an update to strategic development towards the arsenal of organic synthesis

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