Concise synthesis and antitumor activity of Bengamide e and its analogs

Tetrahedron

Volumn 69, Issue 2, 2013, Pages 664-672

  Zhang, Wenxuan ^a   Liang, Qingzhao ^a   Li, Hui ^a   Meng, Xiangbao ^a   Li, Zhongjun ^a  

^a PEKING UNIVERSITY HEALTH SCIENCE CENTER   (China)

Author keywords

Antitumor activity; Bengamide E; Carbohydrate; Stereoselective reduction

Indexed keywords

1,2,3,4 TETRA(BENZYLOXY)HEX 5 EN 1 YL)THIAZOLE; 2 [(1,2,3,4 TETRA(BENZYLOXY)HEX 5 EN 1 YL]THIAZOLE; 2,3,4 TRIHYDROXY 7 METHYL N(2 3 YL)OCT 5 ENAMIDE; 2,3,4 TRIHYDROXY 7 METHYL N(2 OXOAZE PAN 3 YL)OCT 5 ENAMIDE; 2,3,4 TRIHYDROXY 7 METHYL N(2 OXOAZEPAN 3 YL)OCT 5 ENAMIDE; 2,3,4 TRIS(BENZYLOXY) 1 (2 THIAZOLYL)HEX 5 EN 1 OL; 2,3,4 TRIS(BENZYLOXY) 1 METHOXYHEX 5 EN 1 YL)THIAZOLE; 2,3,4 TRIS(BENZYLOXY) 7 METHYL N(2 OXOAZEPAN 3 YL)OCT 5 ENAMIDE; 2,3,4 TRIS(BENZYLOXY) 7 METHYL N(2OXOAZEPAN 3 YL)OCT 5 ENAMIDE; 2,3,4 TRIS(BENZYLOXY) N(2 OXOAZEPAN 3 YL)HEX 5 ENAMIDE; 2,3,4 TRIS(BENZYLOXY)HEX 5 ENOIC ACID; 2,3,4,5 TETRA(BENZYLOXY) 8 METHYL N(2 OXOAZEPAN 3 YL)NON 6 ENAMIDE; 2,3,4,5 TETRA(BENZYLOXY)HEPT 6 ENOIC ACID; 2,3,4,5 TETRA(BENZYLOXY)N(2 OXOAZEPA 3 YL)HEPT 6 ENAMIDE; 2,3,4,5 TETRA(BENZYLOXY)N(2 OXOAZEPAN 3 YL)HEPT 6 ENAMIDE; 2,3,4,5 TETRAHYDROXY 8 METHYL N(2 OXOAZEPAN 3 YL)NON 6 ENAMIDE; 3,4,5 TRIHYDROXY 2 METHOXY 8 METHYL N(2 OXOAZEPAN 3 YL)NON 6 ENAMIDE; 3,4,5 TRIS(BENZYLOXY) 2 METHOXY 8 METHYL N(2 OXOAZEPAN 3 YL)NON 6 ENAMIDE; 3,4,5 TRIS(BENZYLOXY) 2 METHOXY N(2 OXOAZEPAN 3 YL)HEPT 6 ENAMIDE; 3,4,5 TRIS(BENZYLOXY) 2 METHOXY N(2OXOAZEPAN 3 YL)HEPT 6 ENAMIDE; 3,4,5 TRIS(BENZYLOXY) 2 METHOXYHEPT 6 ENOIC ACID; ANTINEOPLASTIC AGENT; BENGAMIDE E; HYDROXYL GROUP; THIAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

ALKYLATION; ANTINEOPLASTIC ACTIVITY; ARTICLE; BREAST CARCINOMA; CANCER CELL; CARCINOMA CELL; CHIRALITY; COLON CANCER; CONTROLLED STUDY; DRUG BINDING; DRUG SYNTHESIS; EPIMER; FEMALE; HUMAN; HUMAN CELL; IC 50; MOLECULAR RECOGNITION; PRIORITY JOURNAL; STEREOCHEMISTRY;

EID: 84877032456     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.11.004     Document Type: Article

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