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Volumn 68, Issue 11, 2012, Pages 2459-2464
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A new application of Baylis-Hillman alcohols to a diastereoselective synthesis of 3-nitrothietanes
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Author keywords
Baylis Hillman adducts; Ionic liquids; Michael addition; O,O Diethyl hydrogen phosphorodithioate; Stereoselective synthesis; Thietanes
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Indexed keywords
3 NITRO 2 PHENYL 4 THIOCYANATOTHIETANE;
3 NITRO 2 PHENYLTHIETANE;
ALCOHOL DERIVATIVE;
ALDEHYDE;
IONIC LIQUID;
NUCLEOPHILE;
PHOSPHORODITHIOIC ACID DERIVATIVE;
PHOSPHOROTHIOIC ACID DERIVATIVE;
THIETANE DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
BAYLIS HILLMAN REACTION;
CHEMICAL REACTION;
CONTROLLED STUDY;
DIASTEREOISOMER;
MICHAEL ADDITION;
PRIORITY JOURNAL;
QUANTUM YIELD;
STEREOCHEMISTRY;
SUBSTITUTION REACTION;
SYNTHESIS;
TRANS ISOMER;
THIA;
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EID: 84857373638
PISSN: 00404020
EISSN: 14645416
Source Type: Journal
DOI: 10.1016/j.tet.2012.01.062 Document Type: Article |
Times cited : (31)
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References (52)
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