About: Enantio- and diastereocontrolled conversion of chiral epoxides to trans-cyclopropane carboxylates: application to the synthesis of cascarillic acid, grenadamide and L-(-)-CCG-II

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About: Enantio- and diastereocontrolled conversion of chiral epoxides to trans-cyclopropane carboxylates: application to the synthesis of cascarillic acid, grenadamide and L-(-)-CCG-II Goto Sponge NotDistinct Permalink

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scientific article published on 26 July 2012

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2012 (fr) наукова стаття, опублікована в липні 2012 (uk) im Juli 2012 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 26 July 2012 (en) artículu científicu espublizáu en xunetu de 2012 (ast)
publication date	wds:Q84622412-C6D650C3-6B75-49B2-858E-722E2B8A03D5
publication date	2012-07-26 00:00:00Z (xsd:dateTime)
author name string	wds:Q84622412-411A79D4-17FC-4965-AA0B-0185EF823812 wds:Q84622412-BBF0BEB4-01BC-4D9B-ACCB-B86FE9C12C3E wds:Q84622412-E6A02BAE-48D0-4AB0-9E2F-11172CC1EB3C
author name string	Pradeep Kumar Abhishek Dubey Anand Harbindu
rdfs:label	Enantio- and diastereocontrolled conversion of chiral epoxides to trans-cyclopropane carboxylates: application to the synthesis of cascarillic acid, grenadamide and L-(-)-CCG-II (en) Enantio- and diastereocontrolled conversion of chiral epoxides to trans-cyclopropane carboxylates: application to the synthesis of cascarillic acid, grenadamide and L-(-)-CCG-II (nl)
skos:prefLabel	Enantio- and diastereocontrolled conversion of chiral epoxides to trans-cyclopropane carboxylates: application to the synthesis of cascarillic acid, grenadamide and L-(-)-CCG-II (en) Enantio- and diastereocontrolled conversion of chiral epoxides to trans-cyclopropane carboxylates: application to the synthesis of cascarillic acid, grenadamide and L-(-)-CCG-II (nl)
name	Enantio- and diastereocontrolled conversion of chiral epoxides to trans-cyclopropane carboxylates: application to the synthesis of cascarillic acid, grenadamide and L-(-)-CCG-II (en) Enantio- and diastereocontrolled conversion of chiral epoxides to trans-cyclopropane carboxylates: application to the synthesis of cascarillic acid, grenadamide and L-(-)-CCG-II (nl)
title	wds:Q84622412-DB0C9659-9DA1-47AE-AB56-1D6ECEFC231C
title	Enantio- and diastereocontrolled conversion of chiral epoxides to trans-cyclopropane carboxylates: application to the synthesis of cascarillic acid, grenadamide and L-(-)-CCG-II (en)
page(s)	wds:Q84622412-36A0EF26-3F15-4F6A-BE17-2041693BAB6C
page(s)	6987-6994
instance of	wds:Q84622412-ACF366B3-8D2F-45A5-BA89-5237484402F9
instance of	scholarly article
main subject	wds:Q84622412-7F7A8DC1-558A-4DFA-955D-5E571DB3F129
main subject	chirality
PubMed ID	wds:Q84622412-0BA3C0D2-2560-4BC5-8753-1314D92E8597
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/22832742
PubMed ID	22832742
published in	wds:Q84622412-6405E4B7-A517-4C95-95B2-CD0EE369EB66
published in	Organic and Biomolecular Chemistry
issue	wds:Q84622412-0E1AE841-02F6-4E8E-97F9-66DBC4823664
volume	wds:Q84622412-53B07012-4B9A-4F0B-85BA-DB04511B6D0A
issue	34
volume	10
DOI	wds:Q84622412-6D1FE90E-994F-48A8-A36D-A36FECF78B1C
DOI	http://dx.doi.org/10.1039/C2OB25622C
DOI	10.1039/C2OB25622C
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q84622412
is cites work of	Discovery, Total Synthesis and Key Structural Elements for the Immunosuppressive Activity of Cocosolide, a Symmetrical Glycosylated Macrolide Dimer from Marine Cyanobacteria Borane catalysed ring opening and closing cascades of furans leading to silicon functionalized synthetic intermediates Anti-addition of Dimethylsulfoxonium Methylide to Acyclic α,β-Unsaturated Ketones and Its Application in Formal Synthesis of an Eicosanoid
is cites work of	wds:Q41147881-A7C3FD2E-EEE9-4B33-B918-645E2B9AC1C6 wds:Q92929412-94F05F0F-3CB9-4B34-8D7F-E74C2E529BDE wds:Q42063828-208C6A8C-D462-4FC8-AA2E-8BFFCE8618AA

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