24398-55-8Relevant academic research and scientific papers
Synthesis of isoquinolines via Rh(III)-catalyzed C-H activation using hydrazone as a new oxidizing directing group
Chuang, Sheng-Chieh,Gandeepan, Parthasarathy,Cheng, Chien-Hong
supporting information, p. 5750 - 5753 (2013/12/04)
An efficient and mechanistically interesting method for the synthesis of highly substituted isoquinolines by a Rh(III)-catalyzed hydrazone directed ortho C-H bond activation and annulation without an external oxidant is described. This reaction is accomplished via a C-C and C-N bond formation along with N-N bond cleavage.
Cu(OAc)2-mediated cross-coupling reaction of benzophenone N,N,N-trimethylhydrazonium salts and aryl boronic acids
Kitamura, Mitsuru,Tokuda, Yu,Tashiro, Norifumi,Okauchi, Tatsuo
, p. 1687 - 1690 (2013/03/13)
Cu(OAc)2-mediated coupling of benzophenone N,N,N- trimethylhydrazonium salts and aryl boronic acids proceeded to afford N-aryl imines.
Synthesis of β-lactams via cycloaddition of hydrazones with phenoxyketene
Sharma,Pandhi
, p. 2196 - 2200 (2007/10/02)
Phenoxyketene is capable of annelating the disubstituted hydrazones to afford stereoselectivity cis-monocyclic β-lactams with a 1-amino functionality. The ease of cycloaddition is governed by substitutents on the azomethine carbon as well as on the hydraz
