Synthesis of highly functionalized 2-thiaspiro[4.5]deca-6,8-dienes via atom efficient tandem Michael addition/Thorpe–Ziegler cyclization-Reference-Cited by-同舟云学术

Synthesis of highly functionalized 2-thiaspiro[4.5]deca-6,8-dienes via atom efficient tandem Michael addition/Thorpe–Ziegler cyclization

Published:2016 Issue:46 Volume:6 Page:40585-40592
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Rani Mani Anusha¹²³⁴⁵,Kumar Sundaravel Vivek¹²³⁴⁵,Roja Somi Santharam¹²³⁴⁵,Almansour Abdulrahman I.⁶⁷⁸⁹¹⁰,Kumar Raju Suresh⁶⁷⁸⁹¹⁰,Athimoolam S.¹¹¹²¹³¹⁴⁵,Kumar Raju Ranjith¹²³⁴⁵

Affiliation:

1. Department of Organic Chemistry

2. School of Chemistry

3. Madurai Kamaraj University

4. Madurai-625 021

5. India

6. Department of Chemistry

7. College of Science

8. King Saud University

9. Riyadh 11451

10. Saudi Arabia

11. Department of Physics

12. University College of Engineering

13. Anna University Constituent College

14. Nagercoil 629 004

Abstract

The reaction of 2,4-bis((Z)-arylidene)dihydrothiophen-3(2H)-ones and 2-(1-arylethylidene)malononitriles proceeded through a tandem sequence of reactions in a single step affording 2-thiaspiro[4.5]deca-6,8-dienes in quantitative yields.

Funder

University Grants Commission

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/RA/C6RA05572A

Reference48 articles.

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2. H. Pellissier , Enantioselective Multicatalysed Tandem Reactions, RSC, ISBN: 978-1-84973-988-7 2014

3. Atom Economy—A Challenge for Organic Synthesis: Homogeneous Catalysis Leads the Way

4. Atom efficiency and catalysis in organic synthesis

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