4-Aminobenzoic Acid → (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal

HRID 1936538Notes

Reaction equation

HRID 1936538 reaction equation
NC1C=CC([C:6](O)=[O:7])=CC=1.N1C=CC(=O)NC1=[O:13].[C@@H:19]1(N2C=CC(=O)NC2=O)[O:27][C@H:24]([CH2:25][OH:26])[C@@H:22]([OH:23])[C@H:20]1[OH:21].[Na+].[Cl-]>>[O:7]=[CH:6][C@@H:25]([C@H:24]([C@@H:22]([C@@H:20]([CH2:19][OH:27])[OH:21])[OH:23])[OH:13])[OH:26]

Participants

5

Reactant 4

HCID 9784-Aminobenzoic Acid2×HCID 1174UracilHCID 5234Sodium ChlorideHCID 6029Uridine

Product 1

HCID 107526(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal

Procedure

For strains which required para-aminobenzoic acid (PABA) for growth, PABA was added to a final concentration of 1 μg/ml. For strains which required uracil and uridine these were added at 20 mM and 10 mM, respectively. Spores were suspended in Tween 80—saline solution (0.025% Tween 80, 0.8% NaCl) and stored at 4° C.

Workup

  1. customstored at 4° C.

Sources & evidence

ORD record
ord-3092d2cc86f342468e49c78c7f659474
Source dataset
uspto-grants-2002_05
Patent number
US06391583B1

Reaction notes

Loading…