BIOMAT Database Logo BIOMAT Database Logo

[Reduction of cyclic imides. II. Reduction of alpha-substituted succinimides and glutarimides by sodium borohydride and their reaction mechanisms]. 1973

T Watanabe, and F Hamaguchi, and S Oki

UI MeSH Term Description Entries
D007094 Imides Organic compounds containing two acyl groups bound to NITROGEN. Imide
D010084 Oxidation-Reduction A chemical reaction in which an electron is transferred from one molecule to another. The electron-donating molecule is the reducing agent or reductant; the electron-accepting molecule is the oxidizing agent or oxidant. Reducing and oxidizing agents function as conjugate reductant-oxidant pairs or redox pairs (Lehninger, Principles of Biochemistry, 1982, p471). Redox,Oxidation Reduction
D011760 Pyrrolidinones A group of compounds that are derivatives of oxo-pyrrolidines. A member of this group is 2-oxo pyrrolidine, which is an intermediate in the manufacture of polyvinylpyrrolidone. (From Merck Index, 11th ed) Pyrrolidinone,Pyrrolidone,Pyrrolidones
D001894 Borohydrides A class of inorganic or organic compounds that contain the borohydride (BH4-) anion. Borohydride
D002621 Chemistry A basic science concerned with the composition, structure, and properties of matter; and the reactions that occur between substances and the associated energy exchange.
D005977 Glutarates Derivatives of glutaric acid (the structural formula (COO-)2C3H6), including its salts and esters. Glutarate
D013388 Succinimides A subclass of IMIDES with the general structure of pyrrolidinedione. They are prepared by the distillation of ammonium succinate. They are sweet-tasting compounds that are used as chemical intermediates and plant growth stimulants. Butanimides,Pyrrolidinediones
D055598 Chemical Phenomena The composition, structure, conformation, and properties of atoms and molecules, and their reaction and interaction processes. Chemical Concepts,Chemical Processes,Physical Chemistry Concepts,Physical Chemistry Processes,Physicochemical Concepts,Physicochemical Phenomena,Physicochemical Processes,Chemical Phenomenon,Chemical Process,Physical Chemistry Phenomena,Physical Chemistry Process,Physicochemical Phenomenon,Physicochemical Process,Chemical Concept,Chemistry Process, Physical,Chemistry Processes, Physical,Concept, Chemical,Concept, Physical Chemistry,Concept, Physicochemical,Concepts, Chemical,Concepts, Physical Chemistry,Concepts, Physicochemical,Phenomena, Chemical,Phenomena, Physical Chemistry,Phenomena, Physicochemical,Phenomenon, Chemical,Phenomenon, Physicochemical,Physical Chemistry Concept,Physicochemical Concept,Process, Chemical,Process, Physical Chemistry,Process, Physicochemical,Processes, Chemical,Processes, Physical Chemistry,Processes, Physicochemical

Related Publications

T Watanabe, and F Hamaguchi, and S Oki
[Reaction of sodium borohydride. II. Reduction of carboxylic acids and esters with sodium borohydride (author's transl)].
December 1976, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
T Watanabe, and F Hamaguchi, and S Oki
Reductive ring openings of glutarimides and barbiturates with sodium borohydride.
January 1968, The Journal of organic chemistry,
T Watanabe, and F Hamaguchi, and S Oki
[Reaction of sodium borohydride. III. Reduction of aromatic nitro compounds with sodium borohydride (author's transl)].
January 1977, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
T Watanabe, and F Hamaguchi, and S Oki
The reaction of substituted ureas with sodium borohydride in pyridine.
February 1969, Tetrahedron letters,
T Watanabe, and F Hamaguchi, and S Oki
[Reduction of cyclic carboxylic anhydrides with sodium borohydride (author's transl)].
November 1975, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
T Watanabe, and F Hamaguchi, and S Oki
[Glutarimides substituted at alpha and beta. Study by spectroscopy and chromatography].
January 1968, Journal de pharmacie de Belgique,
T Watanabe, and F Hamaguchi, and S Oki
The reduction of cozymase by sodium borohydride.
October 1948, The Journal of biological chemistry,
T Watanabe, and F Hamaguchi, and S Oki
Highly enantioselective and regioselective carbonyl reduction of cyclic alpha,beta-unsaturated ketones using TarB-NO2 and sodium borohydride.
October 2009, Organic letters,
T Watanabe, and F Hamaguchi, and S Oki
[Experimental studies with cyclic imides. II. Modification of some somatotropin-dependent processes by cyclic imides].
July 1968, Arzneimittel-Forschung,
T Watanabe, and F Hamaguchi, and S Oki
Sodium borohydride reduction of iodopsin.
June 1975, Vision research,
Copied contents to your clipboard!