One pot synthesis of tetrasubstituted thiophenes: [3 + 2] annulation strategy-Reference-Cited by-同舟云学术

One pot synthesis of tetrasubstituted thiophenes: [3 + 2] annulation strategy

Published:2015 Issue:46 Volume:5 Page:36979-36986
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Sahu Satya Narayan¹²³⁴⁵,Gupta Maneesh Kumar¹²³⁴⁵,Singh Surjeet¹²³⁴⁵,Yadav Pratik¹²³⁴⁵,Panwar Rahul¹²³⁴⁵,Kumar Abhinav¹⁶⁷⁸,Ram Vishnu Ji¹⁶⁷⁸,Kumar Brijesh⁹¹⁰⁷¹¹,Pratap Ramendra¹²³⁴⁵

Affiliation:

1. Department of Chemistry

2. University of Delhi

3. North Campus

4. Delhi

5. India-110007

6. University of Lucknow

7. Lucknow

8. India-226007

9. Division of SAIF

10. Central Drug Research Institute

11. India-226001

Abstract

A simple, efficient and economical synthesis of dimethyl 3-amino-5-(2-oxo-2-arylethyl)thiophene-2,4-dicarboxylates has been reported by ring opening of methyl 3-amino-6-aryl-4-oxo-4H-thieno[3,2-c]pyran-2-carboxylates by alkoxide ions.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA01290B

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5. Synthesis and Characterization of Novel 2-Amino-3-benzoylthiophene Derivatives as Biased Allosteric Agonists and Modulators of the Adenosine A1 Receptor

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