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Total synthesis of (±)-coerulescine and (±)-horsfiline

Wittig olefination–Claisen rearrangement protocol was applied to obtain 3-allyl oxindole. This oxindole was then converted to (±)-coerulescine and (±)-horsfiline.

Detalles Bibliográficos
Autores principales: Kulkarni, Mukund G, Dhondge, Attrimuni P, Chavhan, Sanjay W, Borhade, Ajit S, Shaikh, Yunnus B, Birhade, Deekshaputra R, Desai, Mayur P, Dhatrak, Nagorao R
Formato: Texto
Lenguaje:English
Publicado: Beilstein-Institut 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2982140/
https://www.ncbi.nlm.nih.gov/pubmed/21085515
http://dx.doi.org/10.3762/bjoc.6.103
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author Kulkarni, Mukund G
Dhondge, Attrimuni P
Chavhan, Sanjay W
Borhade, Ajit S
Shaikh, Yunnus B
Birhade, Deekshaputra R
Desai, Mayur P
Dhatrak, Nagorao R
author_facet Kulkarni, Mukund G
Dhondge, Attrimuni P
Chavhan, Sanjay W
Borhade, Ajit S
Shaikh, Yunnus B
Birhade, Deekshaputra R
Desai, Mayur P
Dhatrak, Nagorao R
author_sort Kulkarni, Mukund G
collection PubMed
description Wittig olefination–Claisen rearrangement protocol was applied to obtain 3-allyl oxindole. This oxindole was then converted to (±)-coerulescine and (±)-horsfiline.
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spelling pubmed-29821402010-11-17 Total synthesis of (±)-coerulescine and (±)-horsfiline Kulkarni, Mukund G Dhondge, Attrimuni P Chavhan, Sanjay W Borhade, Ajit S Shaikh, Yunnus B Birhade, Deekshaputra R Desai, Mayur P Dhatrak, Nagorao R Beilstein J Org Chem Full Research Paper Wittig olefination–Claisen rearrangement protocol was applied to obtain 3-allyl oxindole. This oxindole was then converted to (±)-coerulescine and (±)-horsfiline. Beilstein-Institut 2010-09-27 /pmc/articles/PMC2982140/ /pubmed/21085515 http://dx.doi.org/10.3762/bjoc.6.103 Text en Copyright © 2010, Kulkarni et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Kulkarni, Mukund G
Dhondge, Attrimuni P
Chavhan, Sanjay W
Borhade, Ajit S
Shaikh, Yunnus B
Birhade, Deekshaputra R
Desai, Mayur P
Dhatrak, Nagorao R
Total synthesis of (±)-coerulescine and (±)-horsfiline
title Total synthesis of (±)-coerulescine and (±)-horsfiline
title_full Total synthesis of (±)-coerulescine and (±)-horsfiline
title_fullStr Total synthesis of (±)-coerulescine and (±)-horsfiline
title_full_unstemmed Total synthesis of (±)-coerulescine and (±)-horsfiline
title_short Total synthesis of (±)-coerulescine and (±)-horsfiline
title_sort total synthesis of (±)-coerulescine and (±)-horsfiline
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2982140/
https://www.ncbi.nlm.nih.gov/pubmed/21085515
http://dx.doi.org/10.3762/bjoc.6.103
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