A novel three-step hydroxy-deamination sequence: Conversion of lysine to 6-hydroxynorleucine derivatives

DOI: 10.1016/S0040-4039(98)01142-3

Source and publish data:

Tetrahedron Letters p. 5671 - 5674 (1998)

Update date:2022-08-03

Topics: Derivatives Three-Step Sequence Lysine

Authors:

Nevill Jr., C. Richard

Angell, Paul T.

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Article abstract of DOI:10.1016/S0040-4039(98)01142-3

Oxidation of carbamates with catalytic RuO₄, generated from RuO₂ and NaBrO₃, provides the corresponding acyl carbamates, which can be reduced with NaBH₄ to provide alcohols. Application of this methodology to L-lysine provides (S)-6-hydroxynorleucine derivatives.

Full text of DOI:10.1016/S0040-4039(98)01142-3

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