Isolation and synthesis of cryptosanguinolentine (isocryptolepine), a naturally-occurring bioactive indoloquinoline alkaloid

被引:17
|
作者
Thobokholt, Elida N. [1 ]
Larghi, Enrique L. [1 ]
Bracca, Andrea B. J. [1 ]
Kaufman, Teodoro S. [1 ]
机构
[1] Univ Nacl Rosario, Fac Ciencias Bioquim & Farmaceut, CONICET, Inst Quim Rosario,IQUIR, Suipacha 531,S2002LRK, Rosario, Argentina
关键词
PICTET-SPENGLER REACTION; ONE-POT SYNTHESIS; FISCHER INDOLE SYNTHESIS; FORMAL TOTAL-SYNTHESIS; N BOND FORMATION; C-H; CRYPTOLEPIS-SANGUINOLENTA; CATALYZED SYNTHESIS; INDOLE-2,3-DICARBOXYLIC ANHYDRIDES; DECARBOXYLATIVE PALLADATION;
D O I
10.1039/d0ra03096a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cryptosanguinolentine (isocryptolepine) is one of the minor naturally-occurring monomeric indoloquinoline alkaloids, isolated from the West African climbing shrub Cryptolepis sanguinolenta. The natural product displays such a simple and unique skeleton, which chemists became interested in well before it was found in Nature. Because of its structure and biological activity, the natural product has been targeted for synthesis on numerous occasions, employing a wide range of different strategies. Hence, discussed here are aspects related to the isolation of isocryptolepine, as well as the various approaches toward its total synthesis.
引用
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页码:18978 / 19002
页数:25
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