Reagent-controlled stereoselective iodolactonizations
J Haas, S Piguel, T Wirth
Index: Haas, Juergen; Piguel, Sandrine; Wirth, Thomas Organic Letters, 2002 , vol. 4, # 2 p. 297 - 300
Full Text: HTML
Citation Number: 104
Abstract
Iodocyclizations are important transformations and among stereocontrolled iodocyclizations mostly substrate-controlled versions using a chiral auxiliary have been successfully investigated. This work reports on stereoselective reagent-controlled iodolactonizations applying a new method using a combination of ICl and a primary amine leading to the highest selectivities known so far.
Related Articles:
[Nicolai, Stefano; Piemontesi, Cyril; Waser, Jerome Angewandte Chemie - International Edition, 2011 , vol. 50, # 20 p. 4680 - 4683]
[Park, Hyeon; Hong, You-Lee; Kim, Yongjoo B.; Choi, Tae-Lim Organic Letters, 2010 , vol. 12, # 15 p. 3442 - 3445]
[Cottrell, Ian F.; Cowley, Andrew R.; Croft, Laura J.; Hymns, Lauren; Moloney, Mark G.; Nettleton, Ewan J.; Kirsty Smithies; Thompson, Amber L. Tetrahedron, 2009 , vol. 65, # 12 p. 2537 - 2550]
[Petrzilka,M. Helvetica Chimica Acta, 1978 , vol. 61, p. 2286 - 2289]
[Smith,A.B.; Toder,B.H.; Branca,S.J. Journal of the American Chemical Society, 1981 , vol. 103, p. 1996]