Total synthesis of optically active lycopladine a by utilizing diastereoselective protection of carbonyl group in a 1,3-cyclohexanedione derivative

Journal of Organic Chemistry

Volumn 76, Issue 11, 2011, Pages 4522-4532

  Hiroya, Kou ^a   Suwa, Yoshihiro ^a   Ichihashi, Yusuke ^a   Inamoto, Kiyofumi ^a   Doi, Takayuki ^a  

^a TOHOKU UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

1 ,3-CYCLOHEXANEDIONE; CARBON-OXYGEN BONDS; CARBONYL GROUPS; CHIRAL ALCOHOLS; DIASTEREOSELECTIVE; DIKETONES; FORMAL SYNTHESIS; HEMIACETALS; OPTICALLY ACTIVE; SIDE-CHAINS; TOTAL SYNTHESIS;

CARBONYLATION; KETONES;

STEREOSELECTIVITY;

1,3 CYCLOHEXANEDIONE DERIVATIVE; ALCOHOL; CARBON; CARBONYL DERIVATIVE; CYCLOHEXANE DERIVATIVE; DIKETONE; LYCOPLADINE A; NATURAL PRODUCT; OXYGEN; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL BINDING; CHIRALITY; ENANTIOMER; STEREOCHEMISTRY; SYNTHESIS;

CYCLOHEXANONES; KETONES; OPTICAL PROCESSES; SESQUITERPENES; STEREOISOMERISM; SUBSTRATE SPECIFICITY;

EID: 79957806930     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo200418y     Document Type: Article

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