Two efficient methods for the conversion of camptothecin to mappicine ketone, an antiviral lead compound

被引:40
作者
Das, B [1 ]
Madhusudhan, P [1 ]
Kashinatham, A [1 ]
机构
[1] Indian Inst Chem Technol, Organ Chem Div 1, Hyderabad 500007, Andhra Pradesh, India
关键词
D O I
10.1016/S0040-4039(97)10539-1
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Two simple and efficient methods for the conversion of the naturally occurring alkaloid, camptothecin to mappicine ketone, an antiviral lead compound, have been described. The first method involved the treatment of camptothecin with borontrifluoride etherate and the second method utilised the microwave irradiation of the alkaloid. (C) 1997 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:431 / 432
页数:2
相关论文
共 10 条
[1]  
Das B, 1997, INDIAN J CHEM B, V36, P208
[2]  
FORTUNAK JMD, 1994, TETRAHEDRON LETT, V35, P3763
[3]  
GALLO RC, 1971, J NATL CANCER I, V46, P789
[4]   Synthesis of (S)-mappicine and mappicine ketone via radical cascade reaction of isonitriles [J].
Josien, H ;
Curran, DP .
TETRAHEDRON, 1997, 53 (26) :8881-8886
[5]   THE CHEMICAL REARRANGEMENT OF CAMPTOTHECIN TO MAPPICINE KETONE [J].
KINGSBURY, WD .
TETRAHEDRON LETTERS, 1988, 29 (52) :6847-6850
[6]   SYNTHESIS AND ANTI-HSV ACTIVITY OF A-RING-DELETED MAPPICINE KETONE ANALOG [J].
PENDRAK, I ;
BARNEY, S ;
WITTROCK, R ;
LAMBERT, DM ;
KINGSBURY, WD .
JOURNAL OF ORGANIC CHEMISTRY, 1994, 59 (09) :2623-2625
[7]   SYNTHESIS AND ANTI-HSV ACTIVITY OF METHYLENEDIOXY MAPPICINE KETONE ANALOGS [J].
PENDRAK, I ;
WITTROCK, R ;
KINGSBURY, WD .
JOURNAL OF ORGANIC CHEMISTRY, 1995, 60 (09) :2912-2915
[8]   ANTINEOPLASTIC AGENTS FROM PLANTS [J].
WALL, ME ;
WANI, MC .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1977, 17 :117-132
[9]   PLANT ANTITUMOR AGENTS .I. ISOLATION AND STRUCTURE OF CAMPTOTHECIN A NOVEL ALKALOIDAL LEUKEMIA AND TUMOR INHIBITOR FROM CAMPTOTHECA ACUMINATA [J].
WALL, ME ;
WANI, MC ;
COOK, CE ;
PALMER, KH ;
MCPHAIL, AT ;
SIM, GA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1966, 88 (16) :3888-3890
[10]   Nothapodytines A and B from Nothapodytes foetida [J].
Wu, TS ;
Chan, YY ;
Leu, YL ;
Chern, CY ;
Chen, CF .
PHYTOCHEMISTRY, 1996, 42 (03) :907-908