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Volumn 351, Issue 6, 2009, Pages 881-890

Weil-defined regioselective iminopyridine rhodium catalysts for anti-Markovnikov addition of aromatic primary amines to 1-qctyne

Author keywords

Anti Markovnikov addition; Hydroarnina tion reaction; Iminopyridine ligands; Rhodium compounds

Indexed keywords


EID: 65249095666     PISSN: 16154150     EISSN: 15213897     Source Type: Journal    
DOI: 10.1002/adsc.200800786     Document Type: Article
Times cited : (28)

References (57)
  • 54
    • 65249190462 scopus 로고    scopus 로고
    • (E)-2,4,6-Trimethyl-N-octylideneaniline were prepared by combining the aldehyde and 2,4,6-trimethylamine (5 mmol each) in toluene (5 mL) at 23 °C, removing the solvent under vacuum, filtering the toluene solution of the residue through activated silica gel (0.2 g), and concentrating to afford the pure imine.
    • (E)-2,4,6-Trimethyl-N-octylideneaniline were prepared by combining the aldehyde and 2,4,6-trimethylamine (5 mmol each) in toluene (5 mL) at 23 °C, removing the solvent under vacuum, filtering the toluene solution of the residue through activated silica gel (0.2 g), and concentrating to afford the pure imine.
  • 57
    • 65249144146 scopus 로고    scopus 로고
    • SHELXTL-NT version 6.12. Structure Determination Package, Bruker-Nonius AXS. Madison, Wisconsin, USA, 2001
    • SHELXTL-NT version 6.12. Structure Determination Package, Bruker-Nonius AXS. Madison, Wisconsin, USA, 2001.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.