Optically active aminoalcohol derivatives and method of producing same
USRE36718E · kind E · reissue
Assignee
Inventors
Key dates
| Filing date | Mar 30, 1999 |
| Grant date | May 30, 2000 |
| Priority date | — |
| Expiry date | Mar 30, 2019 |
Classification
- Technology area (CPC —)General
Abstract
An object of the present invention is to provide a safe method of commercially producing optically active aminoalcohol derivatives, which serve as intermediates for the synthesis of medicinal chemicals such as the immunopotentiating anticancer agent bestatin, in a simple and easy manner in high yields and with high levels of selectivity. The present invention consists in a method of producing 3-amino-1-nitro-4-phenyl-2-butanol derivatives of the general formula (1) ##STR1## wherein R.sup.1 and R.sup.2 each independently represents a hydrogen atom or an amino group protecting group, and a method of producing 3-amino-2-hydroxy-4-phenylbutyric acid derivatives derivable therefrom.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.