118972-96-6Relevant academic research and scientific papers
Acylative dealkylation of N-tert-butyl-3-substituted azetidines: Facile access to [1.1.0]azabicyclobutane, 3-hydroxyazetidinium hydrochloride, and 3-azetidinones
Dave, Paritosh R.
, p. 5453 - 5455 (1996)
A novel acylative dealkylation of N-tert-butylazetidines and its application to the facile high-yield syntheses of [1.1.0]azabicyclobutane, 3-hydroxyazetidinium hydrochloride, and 3-azetidinones is described.
Photodimerization of N-acetyl-2-azetine: Synthesis of syn- diazatricyclooctane and anti-diazatricyclooctane (diaza-3-ladderane)
Dave, Paritosh R.,Duddu, Rajagopal,Li, Jianchang,Surapaneni, Rao,Gilardi, Richard
, p. 5481 - 5484 (1998)
Photodimerization of N-acetyl-2-azetine to yield both possible head to head dimers with syn and anti geometries is described.
6,5-HETEROCYCLIC PROPARGYLIC ALCOHOL COMPOUNDS AND USES THEREFOR
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Page/Page column 169, (2015/05/06)
The invention relates to novel compounds of Formula I: wherein A, Y, R1, R2 and the subscript b each has the meaning as described herein and compounds of Formula I, and stereoisomers, geometric isomers, tautomers, solvates, metabolites, isotopes, pharmaceutically acceptable salts, or prodrugs thereof. Compounds of Formula I and pharmaceutical compositions thereof are useful in the treatment of disease and disorders in which undesired or over-activation of NF-kB signaling is observed.
Aryloxy and aryloxyalklazetidines as antiarrhythmic and anticonvulsant agents
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, (2008/06/13)
Methods of treating cardiac arrhythmias and convulsions in warm-blooded animas and pharmaceutical compositions therefor are disclosed. The compounds useful in the methods of treatment and compositions are represented by the formula STR1 where n is 0 to 3 and R is H, C1 -C4 alkyl or arylalkyl and Ar is phenyl or substituted phenyl.
Preparation of 3-Oxo- and 3-Ethylideneazetidine Derivatives
Baumann, Hans,Duthaler, Rudolf O.
, p. 1035 - 1041 (2007/10/02)
The preparation of 3-azetidinones with different N-substituents and their transformation to 3-ethylideneazetidines has been studied in relation with a projected synthesis of 3-ethylideneazetidine-2-carboxylic acid (= polyoximic acid; 1).The stable crystal
