A micelle-mediated approach enables facile access to bridged oxabicyclo[<i>n</i>.3.1]alkene scaffolds-Reference-Cited by-同舟云学术

A micelle-mediated approach enables facile access to bridged oxabicyclo[n.3.1]alkene scaffolds

Published:2023 Issue:30 Volume:21 Page:6151-6159
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Wani Mohmad Muzafar¹²,Rashid Auqib¹²,Bhat Bilal A.¹²^ORCID

Affiliation:

1. CSIR-Indian Institute of Integrative Medicine, Sanatnagar, Srinagar-190005, India

2. Academy of Scientific and Innovative Research (AcSIR), Ghaziabad-201002, India

Abstract

The formation of Rauhut–Currier products from 2-cycloalkenones and their deviation to bridged oxabicyclo[n.3.1]alkene constructs by reacting 2-cycloalkenones with 1,3-cycloalkadiones in a micellar medium.

Funder

Council of Scientific and Industrial Research, India

Science and Engineering Research Board

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB00918A

Reference51 articles.

1. Total Synthesis of Natural Products with Bridged Bicyclo[m.n.1] Ring Systems via Type II [5 + 2] Cycloaddition

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4. Structure of (±)-murrafoline, a novel biscarbazole alkaloid from Murraya euchrestifolia

5. Isolation of Fluorescent Benzoxazines with Neuroprotective Activity from the Olive Weevil Pimelocerus perforatus

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