Synthesis of mixed musks <i>via</i> Eschenmoser–Tanabe fragmentation, enyne metathesis and Diels–Alder reaction as key steps-Reference-Cited by-同舟云学术

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Synthesis of mixed musks via Eschenmoser–Tanabe fragmentation, enyne metathesis and Diels–Alder reaction as key steps

Published:2022 Issue:22 Volume:12 Page:14278-14281
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Kotha Sambasivarao¹^ORCID,Agrawal Arpit¹,Tangella Yellaiah¹

Affiliation:

1. Department of Chemistry, Indian Institute of Technology, Bombay, Powai, Mumbai, 400076, Maharashtra, India

Abstract

Musk analogues containing different macrocyclic ring systems as well as different annulated ring systems were synthesised by a simple and useful strategy.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/RA/D2RA01458K

Reference36 articles.

1. Zur Kenntnis des Kohlenstoffringes I. Über die Konstitution des Zibetons

2. A Chemical History of Polycyclic Musks

3. Preparation of macrocyclic musks via olefin metathesis: comparison with classical syntheses and recent advances

4. Study of compositions of musks in different types secreted by forest musk deer (Moschus berezovskii)

5. Long lasting perfume – A review of synthetic musks in WWTPs

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Design of Molecular Diversity by Olefin Metathesis in Tandem with Other Reactions;Synlett;2024-08-05

2. Synthesis of Macrocyclic Musk‐Like Compounds through Ring‐Expansion Metathesis and Tebbe Olefination as Key Steps;ChemistrySelect;2023-08-08

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