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Chemoselective reductions with sodium borohydride

Canadian Journal of Chemistry, 1989
Under the appropriate reaction conditions, sodium borohydride is a highly chemoselective reducing agent. The order of reactivity among carbonyl groups is conjugated enones < ketones < conjugated aldehydes < aldehydes. In general, a carbonyl group of one type can be selectively reduced in the presence of a carbonyl group of a less reactive ...
Dale E. Ward, Chung K. Rhee
openaire   +1 more source

Advances in catalysts for hydrogen production by methanolysis of sodium borohydride

International journal of hydrogen energy, 2022
Tianhao Wang   +3 more
semanticscholar   +1 more source

Sodium Borohydride–Mediated Transesterification

Synthetic Communications, 2010
In the presence of sodium borohydride, esters react with alcohols with formation of the corresponding esters. The reaction is sensitive to the solvent, structure of the ester, and is often concurrent with reduction. Thioesters containing an ester group can be selectively cleaved by the reagent.
Grigoriy Sereda   +2 more
openaire   +1 more source

Sodium borohydride regeneration via direct hydrogen transformation of sodium metaborate tetrahydrate

Journal of Power Sources, 2018
Irreversibility negatively impacts the application of NaBH4 hydrolysis for hydrogen generation. Byproduct regeneration is key to solving this issue. In this work, the direct byproduct of aqueous NaBH4 hydrolysis, NaBO2·4H2O, is reacted with Mg2Si to ...
H. Zhong   +7 more
semanticscholar   +1 more source

Research progress on catalysts for hydrogen generation through sodium borohydride alcoholysis

International journal of hydrogen energy, 2021
Dongyan Xu, Yan Zhang, Qingjie Guo
semanticscholar   +1 more source

Hindered rotation of the borohydride ion in potassium and sodium borohydride

The Journal of Chemical Physics, 1974
The hindered rotational energy levels of the borohydride ion in the high temperature phases of NaBH4 and KBH4 have been computed. The Hamiltonian which describes the motion of the borohydride ion in NaBH4 is invariant under the direct product group Ō × O, while the Hamiltonian for the borohydride ion in KBH4 is invariant under the direct product group ...
openaire   +1 more source

Sodium borohydride reduction of iodopsin

Vision Research, 1975
R S, Fager   +3 more
openaire   +2 more sources

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