Iodine-mediated regioselective 5-endo-dig electrophilic cyclization reaction of selenoenynes: synthesis of selenophene derivatives-Reference-Cited by-同舟云学术

Iodine-mediated regioselective 5-endo-dig electrophilic cyclization reaction of selenoenynes: synthesis of selenophene derivatives

Published:2017 Issue:2 Volume:4 Page:277-282
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Pistoia Renan P.¹²³⁴⁵,Roehrs Juliano A.¹²³⁴⁵,Back Davi F.⁶⁷⁴⁵⁸,Zeni Gilson¹²³⁴⁵^ORCID

Affiliation:

1. Laboratório de Síntese

2. Reatividade

3. Avaliação Farmacológica e Toxicológica de Organocalcogênios CCNE

4. UFSM

5. Santa Maria

6. Laboratório de Materiais Inorgânicos

7. CCNE

8. Brazil 97105-900

Abstract

Selenoenynes underwent electrophilic cyclization reactions with iodine in the presence of an appropriate nucleophile to give 3-iodo-selenophenes and 3-organoselenyl-selenophenes.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/QO/C6QO00491A

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