Diastereoselective synthesis of dihydropyrans via prins cyclization of enol ethers: Total asymmetric synthesis of (+)-civet cat compound

Journal of Organic Chemistry

Volumn 78, Issue 23, 2013, Pages 12182-12188

  Sultana, Sabera ^a   Indukuri, Kiran ^a   Deka, Manash J ^a   Saikia, Anil K ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY GUWAHATI   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ASYMMETRIC SYNTHESIS; DIASTEREOSELECTIVE SYNTHESIS; DIHYDROPYRANS; NATURAL PRODUCTS; PRINS CYCLIZATION; TOTAL SYNTHESIS; TRIFLUOROMETHANESULFONATE; TRIMETHYLSILYL;

ETHERS;

CYCLIZATION;

5,6 DIHYDRO 2H PYRAN 2 ACETATE DERIVATIVE; ACROLEIN; BENZENE DERIVATIVE; DIHYDROPYRAN DERIVATIVE; ENOL ETHER; ETHER DERIVATIVE; LEWIS ACID; NATURAL PRODUCT; PYRAN DERIVATIVE; TRIFLUOROMETHANESULFONIC ACID TRIMETHYLSILYL ESTER; TRIMETHYLSILYL DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; ASYMMETRIC SYNTHESIS; CARBON NUCLEAR MAGNETIC RESONANCE; CIVET (ANIMAL); CONTROLLED STUDY; CYCLIZATION; HYDROLYSIS; METHODOLOGY; STEREOCHEMISTRY;

ANIMALS; BIOLOGICAL PRODUCTS; CYCLIZATION; ETHERS; MOLECULAR STRUCTURE; PYRANS; STEREOISOMERISM; VIVERRIDAE;

EID: 84890209562     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo4015547     Document Type: Article

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