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Volumn 15, Issue 21, 2004, Pages 3467-3476

Axially chiral P,S-heterodonor ligands with a binaphthalene framework for palladium-catalyzed asymmetric allylic substitutions: Experimental investigation on the reversal of enantioselectivity between different alkyl groups on sulfur atom

Author keywords

[No Author keywords available]

Indexed keywords

ACETIC ACID DERIVATIVE; ALKYL GROUP; LIGAND; MALONIC ACID DERIVATIVE; METAL; NAPHTHALENE DERIVATIVE; PALLADIUM; SULFUR;

EID: 7444262096     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetasy.2004.09.027     Document Type: Article
Times cited : (34)

References (55)
  • 9
    • 7444267725 scopus 로고    scopus 로고
    • note
    • (a) MOP (X = OMe) was developed by Hayashi and co-workers, see Ref. 2c:
  • 12
    • 7444266601 scopus 로고    scopus 로고
    • note
    • (c) BINAPS (X = SMe). See Ref. 8
  • 40
    • 7444266598 scopus 로고    scopus 로고
    • note
    • 000 = 752, crystal size: 0.338 × 0.317 × 0.196 mm, data/restraints/parameters = 6723/1/371, final R indices [I > 2σ(I)]: R1 = 0.0562, wR2 = 0.1208, R indices (all data): R1 = 0.0765; wR2 = 0.1400. The crystal structure has been deposited at the Cambridge Crystallographic Data Center and has been allocated the deposition number: CCDC 213071
  • 45
    • 7444255270 scopus 로고    scopus 로고
    • note
    • 000 = 2096; diffractometer: Rigaku AFC7R; residuals: R; Rw: 0.0629, 0.0882. Its crystal structure has been deposited at the Cambridge Crystallographic Data Center and has been allocated the deposition numbers: CCDC 222735
  • 48
    • 1542554559 scopus 로고
    • For a review on Curtin-Hammett kinetics with numerous examples, see: J.I. Seeman Chem. Rev. 83 1983 83
    • (1983) Chem. Rev. , vol.83 , pp. 83
    • Seeman, J.I.1
  • 50
    • 7444250554 scopus 로고    scopus 로고
    • note
    • 3 showed only one signal at 25.22 (ppm) within 1 h, after 2 h later, a new signal at 28.77 appeared besides signal at 25.22


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.