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Neoirietriol
The title compound {systematic name: (1R,4S,4aS,7R,8aR)-4-bromo-7-[(1S,3R)-3-bromo-1,2,2-trimethylcyclopentyl]-1,4a-dimethyldecahydronaphthalene-1,7,8a-triol}, C(20)H(34)Br(2)O(3), is a neoirieane-type bromoditerpenoid isolated from Laurencia yonaguniensis Masuda et Abe, species inedita. The...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006970/ https://www.ncbi.nlm.nih.gov/pubmed/21588005 http://dx.doi.org/10.1107/S1600536810022336 |
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author | Takahashi, Hiroki Takahashi, Yoshinori Suzuki, Minoru Abe, Tsuyoshi Masuda, Michio |
author_facet | Takahashi, Hiroki Takahashi, Yoshinori Suzuki, Minoru Abe, Tsuyoshi Masuda, Michio |
author_sort | Takahashi, Hiroki |
collection | PubMed |
description | The title compound {systematic name: (1R,4S,4aS,7R,8aR)-4-bromo-7-[(1S,3R)-3-bromo-1,2,2-trimethylcyclopentyl]-1,4a-dimethyldecahydronaphthalene-1,7,8a-triol}, C(20)H(34)Br(2)O(3), is a neoirieane-type bromoditerpenoid isolated from Laurencia yonaguniensis Masuda et Abe, species inedita. The absolute stereochemistry was established as (1S,4R,5R,7R,10S,11S,14R). The structure displays inter- and intramolecular O—H⋯O hydrogen bonding. |
format | Text |
id | pubmed-3006970 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30069702010-12-30 Neoirietriol Takahashi, Hiroki Takahashi, Yoshinori Suzuki, Minoru Abe, Tsuyoshi Masuda, Michio Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound {systematic name: (1R,4S,4aS,7R,8aR)-4-bromo-7-[(1S,3R)-3-bromo-1,2,2-trimethylcyclopentyl]-1,4a-dimethyldecahydronaphthalene-1,7,8a-triol}, C(20)H(34)Br(2)O(3), is a neoirieane-type bromoditerpenoid isolated from Laurencia yonaguniensis Masuda et Abe, species inedita. The absolute stereochemistry was established as (1S,4R,5R,7R,10S,11S,14R). The structure displays inter- and intramolecular O—H⋯O hydrogen bonding. International Union of Crystallography 2010-06-26 /pmc/articles/PMC3006970/ /pubmed/21588005 http://dx.doi.org/10.1107/S1600536810022336 Text en © Takahashi et al. 2010 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited. |
spellingShingle | Organic Papers Takahashi, Hiroki Takahashi, Yoshinori Suzuki, Minoru Abe, Tsuyoshi Masuda, Michio Neoirietriol |
title | Neoirietriol |
title_full | Neoirietriol |
title_fullStr | Neoirietriol |
title_full_unstemmed | Neoirietriol |
title_short | Neoirietriol |
title_sort | neoirietriol |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006970/ https://www.ncbi.nlm.nih.gov/pubmed/21588005 http://dx.doi.org/10.1107/S1600536810022336 |
work_keys_str_mv | AT takahashihiroki neoirietriol AT takahashiyoshinori neoirietriol AT suzukiminoru neoirietriol AT abetsuyoshi neoirietriol AT masudamichio neoirietriol |