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Volumn 45, Issue 39, 2004, Pages 7277-7281

Palladium-catalyzed asymmetric tandem allylic substitution using chiral 2-(phosphinophenyl)pyridine ligand

Author keywords

Asymmetric catalysis; P,N ligand; Palladium; Tandem allylic substitution

Indexed keywords

1,2 BIS(BENZYLAMINO)ETHANE; 2 (BENZYLAMINO)PHENOL; 2 (PHOSPHINOPHENYL)PYRIDINE; 2 VINYL 1,4 BENZODIOXANE; 4 BENZYL 2 VINYL 1,4 BENZOXAZINE; ALKANE DERIVATIVE; ALKENE DERIVATIVE; ALLYL COMPOUND; CATECHOL; CHEMICAL COMPOUND; LIGAND; PALLADIUM; PHENOL DERIVATIVE; PYRIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 4444229491     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.08.014     Document Type: Article
Times cited : (51)

References (24)
  • 3
    • 0000687774 scopus 로고    scopus 로고
    • E.N. Jacobsen A. Pfaltz H. Yamamoto Springer Berlin
    • A. Pfaltz, and M. Lautens E.N. Jacobsen A. Pfaltz H. Yamamoto Comprehensive Asymmetric Catalysis Vol. 2 1999 Springer Berlin 833 886
    • (1999) Comprehensive Asymmetric Catalysis , vol.2 , pp. 833-886
    • Pfaltz, A.1    Lautens, M.2
  • 7
  • 20
    • 4444350177 scopus 로고    scopus 로고
    • note
    • 4 and concentrated. Silica gel chromatography of the residue (pentane-diethyl ether = 30:1) gave 2-vinyl-1,4-benzodioxane (20.4 mg, 87%) as an oil. Its ee was determined as described in the footnote to Table 1
  • 21
    • 4444265175 scopus 로고    scopus 로고
    • note
    • α at 20°C. Structural analysis was performed using the teXsan crystallographic software package. The structure was solved by direct methods (SIR92) and expanded using Fourier techniques (DIRDIF94). Some non-hydrogen atoms were refined anisotropically, while the rest were refined isotropically. Hydrogen atoms were refined using the riding model. The Crystallographic data (excluding structure factors) have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication numbers CCDC 244644


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.