Reduction of Some Functional Groups with Zirconium Tetrachloride/Sodium Borohydride

DOI: 10.1055/s-1988-27782

Source and publish data:

Synthesis p. 995 - 996 (1988)

Update date:2022-08-31

Topics:

Authors:

Itsuno, Shinichi

Sakurai, Yoshiki

Ito, Koichi

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1055/s-1988-27782

Novel reducing agent prepared from zirconium tetrachloride and sodium borohydride reduces various functional groups including C=O double bonds, C=N double bonds and CN triple bonds in excellent yield (85-96percent) under mild condition.

Full text of DOI:10.1055/s-1988-27782

Products guided by the article

Product name:Benzyl alcohol

Cas No:100-51-6

Relevant to this article

Engineering of phenylalanine ammonia lyase from Rhodotorula graminis for the enhanced synthesis of unnatural L-amino acids

Doi:10.1016/j.tet.2016.06.026
(2016)
Efficient synthesis of chiral β-seleno amides via ring-opening reaction of 2-oxazolines and their application in the palladium-catalyzed asymmetric allylic alkylation

Doi:10.1021/jo051451a
(2005)
Soluble polyacetylene derivatives by chain-growth polymerization of dienes

Doi:10.1021/ma2004713
(2011)
Nickel-catalyzed cycloaddition of alkynes and isocyanates

Doi:10.1021/ja046477i
(2004)
Synthesis of 3α,6β,7a,12β- And 3α,6β,7β,12β-tetrahydroxy-5β-cholanoic acids

Doi:10.1016/0039-128X(92)90067-J
(1992)
A persubstituted cationic β-cyclodextrin for chiral separations

Doi:10.1021/ac970370e
(1997)

Article Doi

Reduction of Some Functional Groups with Zirconium Tetrachloride/Sodium Borohydride

DOI: 10.1055/s-1988-27782

Source and publish data:

Authors:

Article abstract of DOI:10.1055/s-1988-27782

Full text of DOI:10.1055/s-1988-27782

Products guided by the article

Relevant to this article

Hot Product