Reaktion #546917

ord-6f3cfee9981d4a8d933484091f6148f7

Reaktionsgleichung

NC(=O)c1ccc[n+]([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)OC[C@H]3O[C@@H](n4cnc5c(N)ncnc54)[C@H](O)[C@@H]3O)[C@@H](O)[C@H]2O)c1
NAD+
O=P([O-])([O-])[O-]
phosphate
[Na+].[OH-]
NaOH
NC(=O)C1=CN([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)OC[C@H]3O[C@@H](n4cnc5c(N)ncnc54)[C@H](O)[C@@H]3O)[C@@H](O)[C@H]2O)C=CC1
NADH
Ausbeute 24.2%

Reaktionsbedingungen

Temperatur
23°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe Fisher-Porter bottle was evacuated
  2. 2
    workup.ADDITIONrefilled with argon three times
  3. 3
    SonstigeThe Fisher-Porter bottle was evacuated
  4. 4
    workup.ADDITIONfilled with 70 psi of H2
  5. 5
    SonstigeThe volatiles were removed under reduced pressure
  6. 6
    workup.DISSOLUTIONa sample dissolved in D2O To
  7. 7
    workup.ADDITIONthis was added 20 μl of trimethylsilylpropionate standard solution

Vorschrift

NAD+ (34.0 mg, 38.0 μmol) was placed in 2 mL of a 0.1 M phosphate buffer. The pH of this solution was adjusted to 8.1 with NaOH and then placed in an 80 mL Fisher-Porter bottle. The Fisher-Porter bottle was evacuated and refilled with argon three times then [Cl2Ru(TPPTS)2]2 (6.9 mg, 2.6 μmol) was added under a flow of argon. The Fisher-Porter bottle was evacuated and filled with 70 psi of H2 and stirred to 23° C. for 17.0 hr. The volatiles were removed under reduced pressure and a sample dissolved in D2O To this was added 20 μl of trimethylsilylpropionate standard solution. 1H NMR integration shows that 9.2 μmole of NADH have been produced under these conditions.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07195889B2uspto-grants-2007_03