3349-69-7Relevant academic research and scientific papers
HYDRAZONOPYRROLIDINE DERIVATIVES FOR USE IN PREVENTING AND/OR TREATING DISORDERS ASSOCIATED TO ACINETOBACTER BAUMANNII
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Page/Page column 18; 43-45, (2020/09/08)
The present invention relates to compounds of the following general formula (I): or a pharmaceutically acceptable salt and/or solvate thereof, for use for preventing and/or treating disorders associated to Acinetobacter baumannii. The present invention al
In situ alcohol oxidation-protection reactions
Kiasat,Kazemi,Nourbakhsh
, p. 1555 - 1558 (2007/10/03)
The one-pot conversion of primary and secondary alcohols into phenylhydrazones and 2,4-dintrophenylhydrazones is reported using chromium trioxide supported on silica gel and phenylhydrazines or 2,4- dintrophenylhydrazines under solvent-free conditions. This oxidation arylhydrazone formation reaction has been applied to a range of aliphatic and benzylic alcohols. Copyright Taylor & Francis, Inc.
Rearrangement of 3,3-Disubstituted 1-Aryl-4,5-dihydro-5-oxo-3H-1,2,4-triazolium Tetrafluoroborates; Part 2. A Convenient Synthesis of 1,5-Annulated 1,2-Dihydro-2-phenyl-3H-1,2,4-triazol-3-ones
Gstach, Hubert,Seil, Patrick
, p. 808 - 815 (2007/10/02)
1-Isocyanato-1-(phenylazo)cycloalkanes 3 react with tetrafluoroboric acid to yield 3-spiro substituted 4,5-dihydro-5-oxo-1-phenyl-3H-1,2,4-triazolium tetrafluoroborates 4.Compounds 4 rearrange with ring expansion in good yield to give, after basic workup,
Rearrangement of the N-(3-Oxo-1-butenyl) Derivatives of Hexahydrocycloheptindole and Hexahydrocyclooctindole
Teuber, Hans-Joachim,Gholami, Abbas,Reinehr, Ulrich
, p. 152 - 164 (2007/10/02)
The N-(3-oxo-1-butenyl) derivatives 1,2 of hexahydrocyclohept- and -octindole are rearranged by methanolic hydrochloric acid to give 3a and 4a.Additionally, 3b, 4b, and 5 result. 3a and 4a are transformed into typical derivatives (6,7) and stereoselect
