One-step pathway to selenoisobenzofuran-1(3H)-imine derivatives through highly selective selenocyclization of olefinic amides with benzeneselenyl chloride-Reference-Cited by-同舟云学术

One-step pathway to selenoisobenzofuran-1(3H)-imine derivatives through highly selective selenocyclization of olefinic amides with benzeneselenyl chloride

Published:2018 Issue:12 Volume:16 Page:2150-2155
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Li Xiwang¹²³⁴⁵^ORCID,He Pei¹²³⁴⁵,Zhou Hai-Bing¹²³⁴⁵^ORCID,Dong Chune¹²³⁴⁵^ORCID

Affiliation:

1. State Key Laboratory of Virology

2. Hubei Province Engineering and Technology Research Center for Fluorinated Pharmaceuticals

3. Wuhan University School of Pharmaceutical Sciences

4. Wuhan 430071

5. China

Abstract

A 1,4-diazabicyclo[2.2.2]octane catalyzed selenocyclization of olefinic amides to form various benzeneselenyl substituted isobenzofuran-1(3H)-imine derivatives was achieved under mild reaction conditions.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB00179K

Reference36 articles.

1. Regioselective (Diacetoxyiodo)benzene-Promoted Halocyclization of Unfunctionalized Olefins

2. Solid-Phase Synthesis of Isocoumarins: A Traceless Halocyclization Approach

3. Enantioselective Halocyclization Using Reagents Tailored for Chiral Anion Phase-Transfer Catalysis