HuagongsheHuagongshe Chemistry Print Report · For research reference only
L-Isoleucine → Alloisoleucine, D-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | L-Isoleucine | HCID 6306 | — |
| Reactant | Hydantoin | HCID 10006 | — |
| Reactant | HCID 854211 | HCID 854211 | — |
| Reactant | HCID 86590268 | HCID 86590268 | — |
| Product | Alloisoleucine, D- | HCID 94206 | — |
Reaction Steps
A method for producing D-allo-isoleucine is provided. The method comprises converting L-isoleucine to the corresponding hydantoin. A mixture containing the hydantoin is contacted with a D-hydantoinase to stereoselectively hydrolyze any D-allo-isoleucine hydantoin in the mixture to the corresponding N-carbamoyl-D-allo-isoleucine. The N-carbamoyl-D-allo-isoleucine is decarbamoylated to produce D-allo-isoleucine. Preferably the contacting of the hydantoin with a D-hydantoinase is carried out under conditions permitting the simultaneous epimerization of the chiral center at C-5 of the hydantoin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06822116B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-0b78521188b54b54a72b7c0dbb8e2ea2 |
| Source note | uspto-grants-2004_11 |