Synthesis and reactivities of a novel flavoenzyme model, 5-deazaflavin with C2-symmetry

DOI: 10.1016/S0957-4166(97)00269-3

Source and publish data:

Tetrahedron Asymmetry p. 2319 - 2323 (1997)

Update date:2022-08-04

Topics:

Authors:

Yanada, Reiko

Yoneda, Yoshiyuki

Yazaki, Mikako

Mimura, Norio

Taga, Tooru

Yoneda, Fumio

Yanada, Kazuo

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Article abstract of DOI:10.1016/S0957-4166(97)00269-3

The title model compound represents a redox property of the active site of flavoenzymes and an environmental effect of the apoproteins. Its stereostructure was elucidated by ¹H-NMR spectra and energy minimum calculations. The stereoselectivity of this model was observed during the reaction with Me₂PNPH, as NAD(P)H model.

Full text of DOI:10.1016/S0957-4166(97)00269-3

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