Ethyl ent-15α-[(2-methoxybenzyloxy)methyl]-16-oxobeyeran-20-oate

Ethyl ent-15α-[(2-methoxybenzyloxy)methyl]-16-oxobeyeran-20-oate

The title compound, C31H44O5, was synthesized from isosteviol (systematic name: ent-16-ketobeyeran-19-oic acid). In the molecule, the three six-membered rings adopt chair conformations and the stereochemistry of the A/B and B/C ring junctions are trans. The five-membered ring D adopts an envelope co...

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Main Authors: Ya Wu, Xia Wang, Jian-hong Gong, Chang-yong Wei, Jing-chao Tao
Format: Article
Language:English
Published: International Union of Crystallography 2012-02-01
Series:Acta Crystallographica Section E
Online Access:http://scripts.iucr.org/cgi-bin/paper?S1600536812001833
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spelling doaj-c6ffb140db784d238879f28b423257152020-11-25T00:49:44ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682012-02-01682o495o49510.1107/S1600536812001833Ethyl ent-15α-[(2-methoxybenzyloxy)methyl]-16-oxobeyeran-20-oateYa WuXia WangJian-hong GongChang-yong WeiJing-chao TaoThe title compound, C31H44O5, was synthesized from isosteviol (systematic name: ent-16-ketobeyeran-19-oic acid). In the molecule, the three six-membered rings adopt chair conformations and the stereochemistry of the A/B and B/C ring junctions are trans. The five-membered ring D adopts an envelope conformation with the methylene C atom as the flap.http://scripts.iucr.org/cgi-bin/paper?S1600536812001833
collection DOAJ
language English
format Article
sources DOAJ
author Ya Wu
Xia Wang
Jian-hong Gong
Chang-yong Wei
Jing-chao Tao
spellingShingle Ya Wu
Xia Wang
Jian-hong Gong
Chang-yong Wei
Jing-chao Tao
Ethyl ent-15α-[(2-methoxybenzyloxy)methyl]-16-oxobeyeran-20-oate
Acta Crystallographica Section E
author_facet Ya Wu
Xia Wang
Jian-hong Gong
Chang-yong Wei
Jing-chao Tao
author_sort Ya Wu
title Ethyl ent-15α-[(2-methoxybenzyloxy)methyl]-16-oxobeyeran-20-oate
title_short Ethyl ent-15α-[(2-methoxybenzyloxy)methyl]-16-oxobeyeran-20-oate
title_full Ethyl ent-15α-[(2-methoxybenzyloxy)methyl]-16-oxobeyeran-20-oate
title_fullStr Ethyl ent-15α-[(2-methoxybenzyloxy)methyl]-16-oxobeyeran-20-oate
title_full_unstemmed Ethyl ent-15α-[(2-methoxybenzyloxy)methyl]-16-oxobeyeran-20-oate
title_sort ethyl ent-15α-[(2-methoxybenzyloxy)methyl]-16-oxobeyeran-20-oate
publisher International Union of Crystallography
series Acta Crystallographica Section E
issn 1600-5368
publishDate 2012-02-01
description The title compound, C31H44O5, was synthesized from isosteviol (systematic name: ent-16-ketobeyeran-19-oic acid). In the molecule, the three six-membered rings adopt chair conformations and the stereochemistry of the A/B and B/C ring junctions are trans. The five-membered ring D adopts an envelope conformation with the methylene C atom as the flap.
url http://scripts.iucr.org/cgi-bin/paper?S1600536812001833
work_keys_str_mv AT yawu ethylent15amp9452methoxybenzyloxymethyl16oxobeyeran20oate
AT xiawang ethylent15amp9452methoxybenzyloxymethyl16oxobeyeran20oate
AT jianhonggong ethylent15amp9452methoxybenzyloxymethyl16oxobeyeran20oate
AT changyongwei ethylent15amp9452methoxybenzyloxymethyl16oxobeyeran20oate
AT jingchaotao ethylent15amp9452methoxybenzyloxymethyl16oxobeyeran20oate
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