A novel three-step hydroxy-deamination sequence: Conversion of lysine to 6-hydroxynorleucine derivatives
CR Nevill, PT Angell
Index: Nevill Jr., C. Richard; Angell, Paul T. Tetrahedron Letters, 1998 , vol. 39, # 32 p. 5671 - 5674
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Citation Number: 13
Abstract
Download full text in PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... Oxidation of carbamates with catalytic RuO 4 , generated from RuO 2 and NaBrO 3 , provides the corresponding acyl carbamates, which can be reduced with NaBH 4 to provide alcohols. Application of this methodology to L-lysine provides (S)-6-hydroxynorleucine derivatives.
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