Syntheses of methylenolactocin and nephrosterinic acid via diastereoselective acylation and chemoselective reduction-lactonization

The syntheses of methylenolactocin, nephrosterinic acid and their derivatives can be achieved by using the efficient diastereoselective acylation of dimethyl itaconate-anthracene adduct followed by tandem chemoselective reduction-lactonization. © 2009 Elsevier Ltd. All rights reserved.

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Main Authors:	Rattana Jongkol, Ruangrat Choommongkol, Bongkoch Tarnchompoo, Piyarat Nimmanpipug, Puttinan Meepowpan
Format:	Journal
Published:	2018
Subjects:	Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics
Online Access:	https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=67649840195&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/48859
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Institution:	Chiang Mai University

id	th-cmuir.6653943832-48859
record_format	dspace
spelling	th-cmuir.6653943832-488592018-08-16T02:16:47Z Syntheses of methylenolactocin and nephrosterinic acid via diastereoselective acylation and chemoselective reduction-lactonization Rattana Jongkol Ruangrat Choommongkol Bongkoch Tarnchompoo Piyarat Nimmanpipug Puttinan Meepowpan Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics The syntheses of methylenolactocin, nephrosterinic acid and their derivatives can be achieved by using the efficient diastereoselective acylation of dimethyl itaconate-anthracene adduct followed by tandem chemoselective reduction-lactonization. © 2009 Elsevier Ltd. All rights reserved. 2018-08-16T02:05:56Z 2018-08-16T02:05:56Z 2009-08-08 Journal 00404020 2-s2.0-67649840195 10.1016/j.tet.2009.06.016 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=67649840195&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/48859
institution	Chiang Mai University
building	Chiang Mai University Library
country	Thailand
collection	CMU Intellectual Repository
topic	Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics
spellingShingle	Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics Rattana Jongkol Ruangrat Choommongkol Bongkoch Tarnchompoo Piyarat Nimmanpipug Puttinan Meepowpan Syntheses of methylenolactocin and nephrosterinic acid via diastereoselective acylation and chemoselective reduction-lactonization
description	The syntheses of methylenolactocin, nephrosterinic acid and their derivatives can be achieved by using the efficient diastereoselective acylation of dimethyl itaconate-anthracene adduct followed by tandem chemoselective reduction-lactonization. © 2009 Elsevier Ltd. All rights reserved.
format	Journal
author	Rattana Jongkol Ruangrat Choommongkol Bongkoch Tarnchompoo Piyarat Nimmanpipug Puttinan Meepowpan
author_facet	Rattana Jongkol Ruangrat Choommongkol Bongkoch Tarnchompoo Piyarat Nimmanpipug Puttinan Meepowpan
author_sort	Rattana Jongkol
title	Syntheses of methylenolactocin and nephrosterinic acid via diastereoselective acylation and chemoselective reduction-lactonization
title_short	Syntheses of methylenolactocin and nephrosterinic acid via diastereoselective acylation and chemoselective reduction-lactonization
title_full	Syntheses of methylenolactocin and nephrosterinic acid via diastereoselective acylation and chemoselective reduction-lactonization
title_fullStr	Syntheses of methylenolactocin and nephrosterinic acid via diastereoselective acylation and chemoselective reduction-lactonization
title_full_unstemmed	Syntheses of methylenolactocin and nephrosterinic acid via diastereoselective acylation and chemoselective reduction-lactonization
title_sort	syntheses of methylenolactocin and nephrosterinic acid via diastereoselective acylation and chemoselective reduction-lactonization
publishDate	2018
url	https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=67649840195&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/48859
_version_	1681423305933848576

Syntheses of methylenolactocin and nephrosterinic acid via diastereoselective acylation and chemoselective reduction-lactonization

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