Efforts Directed toward the Synthesis of Colchicine: Application of Palladium-Catalyzed Siloxane Cross-Coupling Methodology
摘要:
Colchicine is an important and synthetically challenging natural product. The key synthetic step in this approach to the synthesis of colchicine involved a palladium-catalyzed cross-coupling reaction between 5-bromotropolone (4) and an aryl siloxane to form the aryl-tropolone bond. The coupling of a variety of highly functionalized aryl siloxane derivatives was investigated and optimized coupling conditions were developed. It was discovered that a palladium catalyst with a high degree of phosphine ligand coordination (5 equiv of phosphine/mol Pd) was necessary to efficiently couple aryl siloxanes with 5-bromotropolone (4). In addition, the coupling approach has provided a direct comparison between siloxane and boronic acid coupling technologies that demonstrated that aryl siloxanes and boronic acids produce similar yields of highly functionalized biaryl products.
Banwell, Martin G.; Cameron, Jennifer M.; Collis, Maree P., Australian Journal of Chemistry, 1991, vol. 44, # 5, p. 705 - 728
作者:Banwell, Martin G.、Cameron, Jennifer M.、Collis, Maree P.、Crisp, Geoffrey T.、Gable, Robert W.、'et al.
DOI:——
日期:——
BANWELL, MARTIN G.;CAMERON, JENNIFER M.;COLLIS, MAREE P.;CRISP, GEOFFREY +, AUSTRAL. J. CHEM., 44,(1991) N, C. 705-728
作者:BANWELL, MARTIN G.、CAMERON, JENNIFER M.、COLLIS, MAREE P.、CRISP, GEOFFREY +
DOI:——
日期:——
Efforts Directed toward the Synthesis of Colchicine: Application of Palladium-Catalyzed Siloxane Cross-Coupling Methodology
作者:W. Michael Seganish、Christopher J. Handy、Philip DeShong
DOI:10.1021/jo051636h
日期:2005.10.1
Colchicine is an important and synthetically challenging natural product. The key synthetic step in this approach to the synthesis of colchicine involved a palladium-catalyzed cross-coupling reaction between 5-bromotropolone (4) and an aryl siloxane to form the aryl-tropolone bond. The coupling of a variety of highly functionalized aryl siloxane derivatives was investigated and optimized coupling conditions were developed. It was discovered that a palladium catalyst with a high degree of phosphine ligand coordination (5 equiv of phosphine/mol Pd) was necessary to efficiently couple aryl siloxanes with 5-bromotropolone (4). In addition, the coupling approach has provided a direct comparison between siloxane and boronic acid coupling technologies that demonstrated that aryl siloxanes and boronic acids produce similar yields of highly functionalized biaryl products.