Biomimetic reduction of inacivated carbonyl compounds by an acid-stable NADH analogue plus brönsted acid

Seiji Shinkai, Hisatake Hamada, Osamu Manabe

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

The NADH model reduction of inactivated carbonyl compounds was achieved by he combination of an acid-stable NADH analogue and strong proton sources (HCl or benzenesulfonic acid).

Original languageEnglish
Pages (from-to)1397-1400
Number of pages4
JournalTetrahedron Letters
Volume20
Issue number16
DOIs
Publication statusPublished - Jan 1 1979

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Carbonyl compounds
Biomimetics
NAD
Acids
Protons
benzenesulfonic acid

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Cite this

Biomimetic reduction of inacivated carbonyl compounds by an acid-stable NADH analogue plus brönsted acid. / Shinkai, Seiji; Hamada, Hisatake; Manabe, Osamu.

In: Tetrahedron Letters, Vol. 20, No. 16, 01.01.1979, p. 1397-1400.

Research output: Contribution to journalArticle

Shinkai, Seiji ; Hamada, Hisatake ; Manabe, Osamu. / Biomimetic reduction of inacivated carbonyl compounds by an acid-stable NADH analogue plus brönsted acid. In: Tetrahedron Letters. 1979 ; Vol. 20, No. 16. pp. 1397-1400.
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