BIOMAT Database Logo BIOMAT Database Logo

O-and N-substituted hydroxylamines. VII. Synthesis of O- and N-benzydrylhydroxylamine and derivatives. 1968

E Bellasio, and F Parravicini, and T La Noce, and E Testa

UI MeSH Term Description Entries
D008722 Methods A series of steps taken in order to conduct research. Techniques,Methodological Studies,Methodological Study,Procedures,Studies, Methodological,Study, Methodological,Method,Procedure,Technique
D001965 Bromides Salts of hydrobromic acid, HBr, with the bromine atom in the 1- oxidation state. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed) Bromide
D002219 Carbamates Derivatives of carbamic acid, H2NC( Carbamate,Aminoformic Acids,Carbamic Acids,Acids, Aminoformic,Acids, Carbamic
D002625 Chemistry, Organic The study of the structure, preparation, properties, and reactions of carbon compounds. (McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed) Organic Chemistry
D006898 Hydroxylamines Organic compounds that contain the (-NH2OH) radical.
D000447 Aldehydes Organic compounds containing a carbonyl group in the form -CHO. Aldehyde
D000478 Alkylation The covalent bonding of an alkyl group to an organic compound. It can occur by a simple addition reaction or by substitution of another functional group. Alkylations
D055601 Organic Chemistry Phenomena The conformation, properties, reaction processes, and the properties of the reactions of organic carbon compounds. Organic Chemistry Concepts,Organic Chemistry Processes,Organic Chemistry Phenomenon,Organic Chemistry Process,Chemistry Process, Organic,Chemistry Processes, Organic,Concept, Organic Chemistry,Concepts, Organic Chemistry,Organic Chemistry Concept,Phenomena, Organic Chemistry,Phenomenon, Organic Chemistry,Process, Organic Chemistry,Processes, Organic Chemistry

Related Publications

E Bellasio, and F Parravicini, and T La Noce, and E Testa
[Synthesis of substituted o-hydroxylamines].
September 1974, Il Farmaco; edizione scientifica,
E Bellasio, and F Parravicini, and T La Noce, and E Testa
[Synthesis of compounds with expected effect on circulatory system. II. New O- and N-substituted derivatives of hydroxylamines].
January 1970, Acta poloniae pharmaceutica,
E Bellasio, and F Parravicini, and T La Noce, and E Testa
Synthesis of N,N,O-Trisubstituted Hydroxylamines by Stepwise Reduction and Substitution of O-Acyl N,N-Disubstituted Hydroxylamines.
April 2016, Organic letters,
E Bellasio, and F Parravicini, and T La Noce, and E Testa
Convenient preparation of O-linked polymer-bound N-substituted hydroxylamines, intermediates for synthesis of N-substituted hydroxamic acids.
September 2000, Organic letters,
E Bellasio, and F Parravicini, and T La Noce, and E Testa
[N-unsubstituted O-acyl-hydroxylamines. 41. Hydroxylamine derivatives].
April 1970, Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft,
E Bellasio, and F Parravicini, and T La Noce, and E Testa
Synthesis of O-tert-Butyl-N,N-disubstituted Hydroxylamines by N-O Bond Formation.
August 2021, Organic letters,
E Bellasio, and F Parravicini, and T La Noce, and E Testa
[Studies on the synthesis of antipyretic analgesics. VII. Synthesis of (N-substituted aminoacyl)urea derivatives].
May 1963, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
E Bellasio, and F Parravicini, and T La Noce, and E Testa
Diversity-Oriented Synthesis of N,N,O-Trisubstituted Hydroxylamines from Alcohols and Amines by N-O Bond Formation.
September 2020, Journal of the American Chemical Society,
E Bellasio, and F Parravicini, and T La Noce, and E Testa
Reactions of cytosine and cytidine with O-substituted hydroxylamines.
January 1975, Journal of the Chemical Society. Perkin transactions 1,
E Bellasio, and F Parravicini, and T La Noce, and E Testa
Pd-Catalyzed C-O Bond Formation Enabling the Synthesis of Congested N,N,O-Trisubstituted Hydroxylamines.
November 2022, Organic letters,
Copied contents to your clipboard!