Synthetic Studies on Camptothecins. Part 3
YY Kuang, JZ Niu, FE Chen
Index: Kuang, Yun-Yan; Niu, Jing-Ze; Chen, Fen-Er Helvetica Chimica Acta, 2010 , vol. 93, # 10 p. 2094 - 2099
Full Text: HTML
Citation Number: 2
Abstract
Abstract A concise and efficient asymmetric process for the total synthesis of (20S)-7-ethyl- 10-hydroxycamptothecin (= SN-38; 1f), an active metabolic form of the prodrug irinotecan, is described. This approach features the enantioselective cyanosilylation of indolizinone 4 into
Related Articles:
[Chemical and Pharmaceutical Bulletin, , vol. 39, # 12 p. 3183 - 3188]
Scalable Synthetic Route to 2-Amino-5-hydroxypropiophenone: Efficient Formal Synthesis of Irinotecan
[Rao, A. V. Rama; Rao, Ramakrishna; Yadav; Khagga, Mukkanti Synthetic Communications, 2013 , vol. 43, # 12 p. 1661 - 1667]
[Drug Metabolism and Disposition, , vol. 41, # 11 p. 1888 - 1895]
[Josien, Hubert; Ko, Sung-Bo; Bom, David; Curran, Dennis P. Chemistry - A European Journal, 1998 , vol. 4, # 1 p. 67 - 83]
[Journal of Organic Chemistry, , vol. 62, # 19 p. 6588 - 6597]