Allyl Alcohol → HCID 70635701, compound
Reaction equation
C(OCC=C)C=C.[K].[CH2:9]([OH:12])[CH:10]=[CH2:11].[CH3:13][C:14]1[CH2:15][S:16][C@@H:17]2[CH:37]([NH:38][C:39](=[O:46])[CH2:40][C:41]3[S:42][CH:43]=[CH:44][CH:45]=3)[C:36](=[O:47])[N:18]2[C:19]=1[C:20]([O:22]C(C1C=CC=CC=1)C1C=CC=CC=1)=[O:21]>>[CH2:9]([O:12][C:37]1([NH:38][C:39](=[O:46])[CH2:40][C:41]2[S:42][CH:43]=[CH:44][CH:45]=2)[C:36](=[O:47])[N:18]2[C:19]([C:20]([OH:22])=[O:21])=[C:14]([CH3:13])[CH2:15][S:16][C@H:17]12)[CH:10]=[CH2:11]Participants
4
Procedure
potassium allyloxide; allyl alcohol; benzhydryl 3-methyl-7-[2-(2-thienyl)acetamido]-3-cephem-4-carboxylate.
Sources & evidence
- ORD record
- ord-e93320e8d6ac48fabb129d72aee2a10f
- Source dataset
- uspto-grants-1976_11
- Patent number
- US03994885
Reaction notes
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