Selectivity in the acid catalysed reduction of carbonyl compounds to alcohols by bis(triphenylphosphine)copper(I) tetrahydroborate: Reduction of aldehydes in the presence of ketones-Reference-Cited by-同舟云学术

Selectivity in the acid catalysed reduction of carbonyl compounds to alcohols by bis(triphenylphosphine)copper(I) tetrahydroborate: Reduction of aldehydes in the presence of ketones

Published:1981-01 Issue:7 Volume:22 Page:675-678
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Fleet G.W.J.,Harding P.J.C.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference12 articles.

1. Selective reduction of aldehydes

2. Stereochemistry and mechanism of ketone reductions by hydride reagents

3. Quantitative prediction of stereochemistry in the reduction of cyclohexanones by sodium borohydride

4. Reduction of Cyclic and Bicyclicc Ketones by Complex Metal Hydrides

5. μ-Bis(cyanotrihydroborato)-tetrakis(triphenylphosphine) dicopper(I). A new, selective, pH dependent reducing agent

Cited by 53 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Preparation, reactivity and photoluminescence of copper(I) borohydride complexes with bis[(2-diphenylphosphino)phenyl] ether as chelating ligand;Journal of Organometallic Chemistry;2022-01

2. Synthesis, crystal and structural characterization, Hirshfeld surface analysis and DFT calculations of three symmetrical and asymmetrical phosphonium salts;Journal of Molecular Structure;2021-10

3. Formation of Alcohols and Phenols by Reduction of Carbonyl Compounds;Comprehensive Organic Transformations;2018-02-28

4. Binuclear Copper(I) Borohydride Complex Containing Bridging Bis(diphenylphosphino) Methane Ligands: Polymorphic Structures of [(µ2-dppm)2Cu2(η2-BH4)2] Dichloromethane Solvate;Crystals;2017-10-20

5. Poly(vinylpyrrolidone)-Grafted Silica as Polymeric Cosolvent Catalyst for Chemoselective Reduction of Aldehydes and Ketones to Alcohols;Iranian Journal of Science and Technology, Transactions A: Science;2017-09