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Volumn , Issue 14, 2010, Pages 2130-2132
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First enantioselective total synthesis of the reported structure of (R)-(+)-Orizaterpenyl benzoate using an asymmetric allylation of a prochiral ketone in a domino process
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Author keywords
allylsilane; asymmetric allylation; domino reactions; natural products; ozonolysis; tertiary homoallylic alcohols
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Indexed keywords
2 AMINOPYRIDINE DERIVATIVE;
3 HYDROXY 3,7 DIMETHYLOCTYLBENZOATE;
3,5 DINITROBENZOATE DERIVATIVE;
4,8 DIMETHYL 4 (1,2 DIPHENYLETHOXY)NONENE;
BENZOIC ACID DERIVATIVE;
KETONE;
N,N DIMETHYL 2 AMINOPYRIDINE;
ORIZATERPENYLBENZOATE;
UNCLASSIFIED DRUG;
ALLYLATION;
ARTICLE;
CHEMICAL INTERACTION;
CHEMICAL REACTION;
CHEMICAL STRUCTURE;
CHIRALITY;
CRYSTALLIZATION;
DEPROTECTION REACTION;
ENANTIOMER;
ENANTIOSELECTIVITY;
ESTERIFICATION;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
HYDROGENOLYSIS;
HYDROLYSIS;
PURIFICATION;
STRUCTURE ANALYSIS;
SYNTHESIS;
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EID: 77956030334
PISSN: 09365214
EISSN: 14372096
Source Type: Journal
DOI: 10.1055/s-0030-1258537 Document Type: Article |
Times cited : (7)
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References (12)
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