A convenient base-mediated synthesis of 3-aryol-4-methyl (or benzyl)-2-methylthio furans from α-oxo ketene dithioacetals and propargyl alcohols via domino coupling/annulations-Reference-Cited by-同舟云学术

A convenient base-mediated synthesis of 3-aryol-4-methyl (or benzyl)-2-methylthio furans from α-oxo ketene dithioacetals and propargyl alcohols via domino coupling/annulations

Published:2014 Issue:44 Volume:12 Page:8947-8951
ISSN:1477-0520
Container-title:Org. Biomol. Chem.
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Yang Xiaobing¹²³⁴³,Hu Fangzhong¹²³⁴³,Di Hongjing¹²³⁴³,Cheng Xinxin¹²³⁴³,Li Dan¹²³⁴³,Kan Xiaoli¹²³⁴³,Zou Xiaomao¹²³⁴³,Zhang Qichun⁵⁶⁷

Affiliation:

1. State Key Laboratory and Institute of Elemento-Organic Chemistry

2. Nankai University

3. Tianjin 300071, China

4. Collaborative Innovation Center of Chemical Science and Engineering (Tianjin)

5. School of Materials Science Engineering

6. Nanyang Technological University

7. , Singapore

Abstract

A convenient base-mediated synthesis of 3-aryol-4-methyl (or benzyl)-2-methylthio furans2has been developed through the domino coupling/annulations from α-oxo ketene dithioacetals1and propargyl alcohols.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/OB/C4OB01300J

Reference64 articles.

1. α-Oxo ketene dithioacetals and related compounds: versatile three-carbon synthons

2. α-Oxoketene-S,S-, N,S- and N,N-acetals: Versatile intermediates in organic synthesis

3. Recent developments of ketene dithioacetal chemistry

4. Synthesis of 2,5-furanocycles through intraannular cyclization of macrocyclic allenones

5. Total Synthesis of the Pseudopterane (.+-.)-Kallolide B

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