Step-wise and one-pot synthesis of highly substituted conjugated trienes from 2-oxobenzo[h]chromenes/2H-pyran-2-ones-Reference-Cited by-同舟云学术

Step-wise and one-pot synthesis of highly substituted conjugated trienes from 2-oxobenzo[h]chromenes/2H-pyran-2-ones

Published:2021 Issue:17 Volume:19 Page:3901-3910
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Elagamy Amr¹²³⁴^ORCID,Althagafi Ismail⁵⁶⁷⁸⁹,Pratap Ramendra¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. University of Delhi

3. Delhi

4. India

5. Chemistry Department

6. Faculty of Science

7. Umm Al-Qura University

8. 21955 Makkah

9. Saudi Arabia

Abstract

The synthesis of conjugated trienes by ring contraction of 2-oxobenzo[h]chromenes/2H-pyran-2-ones followed by decarboxylative rearrangement has been developed.

Funder

Department of Biotechnology, Ministry of Science and Technology, India

The World Academy of Sciences

University of Delhi

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/OB/D1OB00314C

Reference36 articles.

1. Synthesis of ethyl (13E)-trifluoromethylretinoate and its analogues by palladium-catalysed cross-coupling

2. Stereoselective Synthesis of All-trans-, (13Z)- and (9-nor)-Retinoic Acids via Stille Reaction

3. AN EXPEDIENT STEREOCONTROLLED SYNTHESIS OF 7-CIS-RETINOIDS

4. A Pericyclic Cascade to the Stereocontrolled Synthesis of 9-cis-Retinoids

5. Stereoselective synthesis of substituted 1,3,5-hexatrienes from diallylic sulfones

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