HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methyl-4-Prop-1-En-2-Ylcyclohexene → N-CBZ-S-(1-(4-methylcyclohex-3-enyl)isopropyl)-L-cysteine methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methyl-4-Prop-1-En-2-Ylcyclohexene | HCID 22311 | — |
| Reactant | Methyl (2R)-2-{[(benzyloxy)carbonyl]amino}-3-sulfanylpropanoate | HCID 11391550 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-CBZ-S-(1-(4-methylcyclohex-3-enyl)isopropyl)-L-cysteine methyl ester | HCID 131715037 | — |
Reaction Steps
The ether is prepared from N-CBZ-L-cysteine methyl ester and α-limonene in a manner similar to that described in Example 1B. The product can be characterized by NMR spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04676989 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-1a9b5d3ea53e4527a40b117876aec43d |
| Source note | uspto-grants-1987_06 |