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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1447468Generated: November 2, 2026

(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal → HCID 13018026, compound

https://huagongshe.com/reaction/1447468

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 107526—
ReactantHCID 131712426HCID 131712426—
ProductHCID 13018026HCID 13018026—

Reaction Steps

Clostridium acetobutylicum IFO 3346 is inoculated in 100 ml of Potato Dextrose Broth (product of DIFCO Lab.). Air in the fermentor is replaced with sterilized nitrogen gas and the fermentor is sealed. Culturing is carried out at a temperature of 30° C. for 48 hours. After the cultivation, cells are recovered, washed with physiological saline solution and suspended in 2 ml of 1/30 M potassium phosphate buffer (pH 7.0). 0.5 ml of the substrate solution prepared as in Example 5 and the cell suspension are combined and allowed to react at a temperature of 30° C. for 20 hours. The reaction is monitored as in Example 5. (-)-cis-7-[(R)-2-phenyl-2-aminoacetamido]-1-azabicyclo[4,2,0]oct-2-en-8-on-2-carboxylic acid is remained unchanged and only (+)-cis-7-[(R)-2-phenyl-2-aminoacetamido]-1-azabicyclo[4,2,0]oct-2-en-8-on-2-carboxylic acid is decreased. The amount of the decrease is 1.0 mg, producing 0.2 mg of (+)-7-amino-1-azabicyclo[4,2,0]oct-2-en-8-on-2-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04316958
Source datasetuspto-grants-1982_02
ORD IDord-053bfaa978394d2dafa438a4eafdffa9
Source noteuspto-grants-1982_02