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

Musk analogues containing different macrocyclic ring systems as well as different annulated ring systems were synthesised by a simple and useful strategy. This strategy includes Eschenmoser–Tanabe fragmentation, enyne metathesis and Diels–Alder reaction as key steps. Starting from easily available (...

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Detalles Bibliográficos
Autores principales: Kotha, Sambasivarao, Agrawal, Arpit, Tangella, Yellaiah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092383/
https://www.ncbi.nlm.nih.gov/pubmed/35558836
http://dx.doi.org/10.1039/d2ra01458k
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author Kotha, Sambasivarao
Agrawal, Arpit
Tangella, Yellaiah
author_facet Kotha, Sambasivarao
Agrawal, Arpit
Tangella, Yellaiah
author_sort Kotha, Sambasivarao
collection PubMed
description Musk analogues containing different macrocyclic ring systems as well as different annulated ring systems were synthesised by a simple and useful strategy. This strategy includes Eschenmoser–Tanabe fragmentation, enyne metathesis and Diels–Alder reaction as key steps. Starting from easily available (n) macrocyclic ketones, (n + 3) macrocyclic systems were assembled using the basic organic reactions.
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spelling pubmed-90923832022-05-11 Synthesis of mixed musks via Eschenmoser–Tanabe fragmentation, enyne metathesis and Diels–Alder reaction as key steps Kotha, Sambasivarao Agrawal, Arpit Tangella, Yellaiah RSC Adv Chemistry Musk analogues containing different macrocyclic ring systems as well as different annulated ring systems were synthesised by a simple and useful strategy. This strategy includes Eschenmoser–Tanabe fragmentation, enyne metathesis and Diels–Alder reaction as key steps. Starting from easily available (n) macrocyclic ketones, (n + 3) macrocyclic systems were assembled using the basic organic reactions. The Royal Society of Chemistry 2022-05-11 /pmc/articles/PMC9092383/ /pubmed/35558836 http://dx.doi.org/10.1039/d2ra01458k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Kotha, Sambasivarao
Agrawal, Arpit
Tangella, Yellaiah
Synthesis of mixed musks via Eschenmoser–Tanabe fragmentation, enyne metathesis and Diels–Alder reaction as key steps
title Synthesis of mixed musks via Eschenmoser–Tanabe fragmentation, enyne metathesis and Diels–Alder reaction as key steps
title_full Synthesis of mixed musks via Eschenmoser–Tanabe fragmentation, enyne metathesis and Diels–Alder reaction as key steps
title_fullStr Synthesis of mixed musks via Eschenmoser–Tanabe fragmentation, enyne metathesis and Diels–Alder reaction as key steps
title_full_unstemmed Synthesis of mixed musks via Eschenmoser–Tanabe fragmentation, enyne metathesis and Diels–Alder reaction as key steps
title_short Synthesis of mixed musks via Eschenmoser–Tanabe fragmentation, enyne metathesis and Diels–Alder reaction as key steps
title_sort synthesis of mixed musks via eschenmoser–tanabe fragmentation, enyne metathesis and diels–alder reaction as key steps
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092383/
https://www.ncbi.nlm.nih.gov/pubmed/35558836
http://dx.doi.org/10.1039/d2ra01458k
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AT tangellayellaiah synthesisofmixedmusksviaeschenmosertanabefragmentationenynemetathesisanddielsalderreactionaskeysteps

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