249296-51-3Relevant academic research and scientific papers
Urethane group directed reductive couplings mediated by SmI2
Matsuda, Fuyuhiko,Kawatsura, Motoi,Dekura, Fumiko,Shirahama, Haruhisa
, p. 2371 - 2375 (1999)
The SmI2-induced ketone-olefm coupling reactions of a-(alkoxycarbonyl)amino ketones 1 and 3 with methyl, ethyl, isopropyl, and tert-buty] crotohate took place with high stereocontrol about the new chiral centers providing the j)V!-l,2-amino alcohol products, sys-trans-γ-lactones 1 and 4, in excellent yields. Apparently, the stereochemical course of these reductive couplings is stereocontrolled by chelation of the Sm(in) cations attached to the resulting ketyl radicals with the urethane groups. Stereoselectivity increased as the size of the alkyl group of the esters of crotonic acid increased. In particular, 2 and 4 were almost exclusively obtained when the SmI2-induced couplings of 1 and 3 were carried out with rc;7-butyl crotonate. Interestingly, the hydroxy group-directed couplings induced by SmI2 of the a-hydroxy ketone 11 with methyl, ethyl, and isopropyl crotonate proceeded with a complete reversal of diastereoselectivity, almost exclusively providing the syn-l,2-diol product, yn-c/s-y-lactone 12.
