Butterflyene: an entry into an aesthetically pleasing carbocycle <i>via</i> a Diels–Alder reaction on a tetrasubstituted olefin-Reference-Cited by-同舟云学术

Butterflyene: an entry into an aesthetically pleasing carbocycle via a Diels–Alder reaction on a tetrasubstituted olefin

Published:2023 Issue:39 Volume:21 Page:7917-7923
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Bhatt Gaurang J.¹^ORCID,Deota Pradeep T.¹^ORCID,Som Narayan N.²^ORCID,Shah Darshil³^ORCID

Affiliation:

1. Department of Applied Chemistry, Faculty of Technology & Engineering, The Maharaja Sayajirao University of Baroda, Vadodara-390 001, Gujarat, India

2. Materials Design Division, Faculty of Materials Science and Engineering, Warsaw University of Technology, 141 Wołoska Str., 02-507 Warsaw, Poland

3. Department of Chemical Engineering, Faculty of Technology & Engineering, The Maharaja Sayajirao University of Baroda, Vadodara-390 001, Gujarat, India

Abstract

An aesthetically pleasing prototype decacyclic ring system resembling the shape of a butterfly has been synthesized in four simple steps. Diels–Alder reactions on a tetrasubstituted double bond give rise to the formation of its analogues.

Funder

Department of Science & Technology, Ministry of Science and Technology, India

Human Resource Development Group

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB01056B

Reference22 articles.

1. Relieving the stress together: annulation of two different strained rings towards the formation of biologically significant heterocyclic scaffolds

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