SmI2-mediated reductive cyclization of β-arylthio ketones: a facile and diastereoselective synthesis of thiochroman derivatives-Reference-Cited by-同舟云学术

SmI2-mediated reductive cyclization of β-arylthio ketones: a facile and diastereoselective synthesis of thiochroman derivatives

Published:2017 Issue:29 Volume:15 Page:6157-6166
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Mao Hui¹²³⁴⁵,You Bing-Xin¹²³⁴⁵,Zhou Lie-Jin¹²³⁴⁵,Xie Ting-Ting¹²³⁴⁵,Wen Yi-Hang¹²³⁴⁵,Lv Xin¹²³⁴⁵^ORCID,Wang Xiao-Xia¹²³⁴⁵^ORCID

Affiliation:

1. Department of Chemistry

2. College of Chemistry and Life Sciences

3. Zhejiang Normal University

4. Jinhua 321004

5. People's Republic of China

Abstract

SmI₂-mediated reductive cyclization of β-arylthio ketones afforded a general approach to dihydrothiochroman-ols in good yields and high degrees of diastereoselectivity.

Funder

Natural Science Foundation of Zhejiang Province

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/2017/OB/C7OB01082F

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