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Volumn , Issue 19, 2009, Pages 3668-3670

Controllable synthesis of P-chiral 1,2- and 1,3-diphosphines via asymmetric Diels-Alder reactions involving functionalized allylic phosphines as dienophiles

Author keywords

[No Author keywords available]

Indexed keywords

CONTROLLABLE SYNTHESIS; DIELS-ALDER REACTION; DIENOPHILES; DIPHOSPHINES; FUNCTIONALIZED; ORGANOPALLADIUM COMPLEXES;

EID: 67249141463     PISSN: 14779226     EISSN: 14779234     Source Type: Journal    
DOI: 10.1039/b904090k     Document Type: Article
Times cited : (11)

References (14)
  • 11
    • 35848960807 scopus 로고    scopus 로고
    • 31P NMR signal at δ 31.9 ppm appears in the process, which may be due to the reactive species trans-R- 2. However, trans-R- 2 could not be isolated. Double bond migration in N-allylic systems:
    • M. Ma S. A. Pullarkat Y. Li P. H. Leung Inorg. Chem. 2007 46 9488
    • (2007) Inorg. Chem. , vol.46 , pp. 9488
    • Ma, M.1    Pullarkat, S.A.2    Li, Y.3    Leung, P.H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.