HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydantoin → Alloisoleucine, D-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydantoin | HCID 10006 | — |
| Reactant | HCID 854211 | HCID 854211 | — |
| Reactant | HCID 69816793 | HCID 69816793 | — |
| Product | Alloisoleucine, D- | HCID 94206 | — |
Reaction Steps
Preferably in the claimed method 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. As discussed further below, the simultaneous epimerization permits the reaction to be carried out to substantial completion so that L-isoleucine hydantoin is converted to N-carbamoyl-D-allo-isoleucine. The N-carbamoyl-D-allo-isoleucine is then decarbamoylated to produce D-allo-isoleucine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06822116B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-8c09f882d44348ec9d94062ff274fe60 |
| Source note | uspto-grants-2004_11 |