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Volumn 51, Issue 33, 2010, Pages 4425-4428
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Stereoselective construction of quaternary chiral centers using Ti(III)-mediated opening of 2,3-epoxy alcohols: Studies directed toward the synthesis of penifulvins
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Author keywords
Penifulvin; Quaternary chiral center; Radical cyclization; Ti(III) mediated epoxide opening
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Indexed keywords
ALCOHOL DERIVATIVE;
ESTER;
INSECTICIDE;
PENIFULVIN A;
PENIFULVIN B;
PENIFULVIN C;
PENIFULVIN D;
PENIFULVIN E;
RADICAL;
TITANIUM;
UNCLASSIFIED DRUG;
ARTICLE;
CHEMICAL STRUCTURE;
CHIRALITY;
CYCLIZATION;
DIASTEREOISOMER;
MICHAEL ADDITION;
NUCLEAR OVERHAUSER EFFECT;
OXIDATION;
RING OPENING;
STEREOCHEMISTRY;
SYNTHESIS;
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EID: 77955412455
PISSN: 00404039
EISSN: None
Source Type: Journal
DOI: 10.1016/j.tetlet.2010.06.076 Document Type: Article |
Times cited : (19)
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References (29)
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