Synthesis of both enantiomers of halitunal

Both enantiomers of halitunal (1), a novel diterpene aldehyde having an iridoid carbon framework with a heteroaromatic 10π-system, have been synthesized from (+)-genipin (2).

Detalles Bibliográficos
Autores principales: Shimano, Kazunori, Ge, Yuting, Sakaguchi, Kazuhiko, Isoe, Sachihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Ltd. 1996
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127712/
http://dx.doi.org/10.1016/0040-4039(96)00268-7
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author Shimano, Kazunori
Ge, Yuting
Sakaguchi, Kazuhiko
Isoe, Sachihiko
author_facet Shimano, Kazunori
Ge, Yuting
Sakaguchi, Kazuhiko
Isoe, Sachihiko
author_sort Shimano, Kazunori
collection PubMed
description Both enantiomers of halitunal (1), a novel diterpene aldehyde having an iridoid carbon framework with a heteroaromatic 10π-system, have been synthesized from (+)-genipin (2).
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spelling pubmed-71277122020-04-08 Synthesis of both enantiomers of halitunal Shimano, Kazunori Ge, Yuting Sakaguchi, Kazuhiko Isoe, Sachihiko Tetrahedron Lett Article Both enantiomers of halitunal (1), a novel diterpene aldehyde having an iridoid carbon framework with a heteroaromatic 10π-system, have been synthesized from (+)-genipin (2). Published by Elsevier Ltd. 1996-03-25 1998-09-10 /pmc/articles/PMC7127712/ http://dx.doi.org/10.1016/0040-4039(96)00268-7 Text en Copyright © 1996 Published by Elsevier Ltd. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Shimano, Kazunori
Ge, Yuting
Sakaguchi, Kazuhiko
Isoe, Sachihiko
Synthesis of both enantiomers of halitunal
title Synthesis of both enantiomers of halitunal
title_full Synthesis of both enantiomers of halitunal
title_fullStr Synthesis of both enantiomers of halitunal
title_full_unstemmed Synthesis of both enantiomers of halitunal
title_short Synthesis of both enantiomers of halitunal
title_sort synthesis of both enantiomers of halitunal
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127712/
http://dx.doi.org/10.1016/0040-4039(96)00268-7
work_keys_str_mv AT shimanokazunori synthesisofbothenantiomersofhalitunal
AT geyuting synthesisofbothenantiomersofhalitunal
AT sakaguchikazuhiko synthesisofbothenantiomersofhalitunal
AT isoesachihiko synthesisofbothenantiomersofhalitunal

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