Production Method 1

53-84-9

10021-11-1

Reaction Conditions

1.1R:C:9028-53-9

Reference

α-Secondary Isotope Effects as Probes of "Tunneling-Ready" Configurations in Enzymatic H-Tunneling: Insight from Environmentally Coupled Tunneling Models

By Pudney, Christopher R. et al, Journal of the American Chemical Society, 2006, 128(43), 14053-14058

Production Method 2

53-84-9

10021-11-1

Reaction Conditions

1.1S:H2O, 80 min, 20°C, pH 7.5

Reference

Stereochemical Outcome at Four Stereogenic Centers during Conversion of Prephenate to Tetrahydrotyrosine by BacABGF in the Bacilysin Pathway

By Parker, Jared B. and Walsh, Christopher T., Biochemistry, 2012, 51(28), 5622-5632

Production Method 3

53-84-9

10021-11-1

Reaction Conditions

1.1R:C:9001-40-5, S:H2O, 28 h

Reference

Secoisolariciresinol dehydrogenase: mode of catalysis and stereospecificity of hydride transfer in Podophyllum peltatum

By Moinuddin, Syed G. A. et al, Organic & Biomolecular Chemistry, 2006, 4(5), 808-816

Adenosine 5'-(trihydrogen diphosphate), P'→5'-ester with (4S)-1,4-dihydro-1-β-D-ribofuranosyl-3-pyridine-4-d-carboxamide Raw materials

• b-Nicotinamide Adenine Dinucleotide

Adenosine 5'-(trihydrogen diphosphate), P'→5'-ester with (4S)-1,4-dihydro-1-β-D-ribofuranosyl-3-pyridine-4-d-carboxamide Preparation Products

• Adenosine 5'-(trihydrogen diphosphate), P'→5'-ester with (4S)-1,4-dihydro-1-β-D-ribofuranosyl-3-pyridine-4-d-carboxamide (10021-11-1)

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