Stereoselective synthesis and biological studies of the C2 and C3 epimer and the enantiomer of pachastrissamine (Jaspine B)

Synthesis

Volumn , Issue 1, 2010, Pages 115-119

  Jayachitra, G ^a   Sudhakar, N ^a   Anchoori, Ravi Kumar ^a   Rao, B Venkateswara ^a   Roy, Sayantani ^a   Banerjee, Rajkumar ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

Cytotoxicity; D glucose; Jaspine B; Mitsunobu inversion; Pachastrissamine; Wittig olefination

Indexed keywords

ANTICANCER DRUG; BIOLOGICAL STUDIES; D-GLUCOSE; EPIRUBICIN; MCF-7 CELLS; MITSUNOBU INVERSION; PACHASTRISSAMINE (JASPINE B); STEREOSELECTIVE SYNTHESIS; WITTIG OLEFINATION;

CHIRALITY; ENANTIOMERS; STEREOSELECTIVITY;

GLUCOSE;

4 ACETAMIDO 2 TETRADECYLTETRAHYDROFURAN 3 YL ACETATE; 4 AMINO 2 TETRADECYLTETRAHYDROFURAN 3 OL; 4 AMINO 2 TETRADECYLTETRAHYDROFURAN 3 OL TRIFLUOROACETIC ACID; ANTINEOPLASTIC AGENT; EPIRUBICIN; GLUCOSE; PACHASTRISSAMINE; SPHINGOSINE DERIVATIVE; UNCLASSIFIED DRUG;

ANTINEOPLASTIC ACTIVITY; ARTICLE; CELL STRAIN MCF 7; CONTROLLED STUDY; DRUG CYTOTOXICITY; DRUG SYNTHESIS; ENANTIOMER; EPIMER; FEMALE; HUMAN; HUMAN CELL; IC 50; STEREOCHEMISTRY; STEREOISOMERISM;

EID: 75749091489     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0029-1217096     Document Type: Article

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