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Volumn 53, Issue 10, 1997, Pages 3513-3526

Asymmetric allylation of aromatic aldehydes catalyzed by chiral phosphoramides prepared from (S)-proline

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE; ALLYL COMPOUND; PHOSPHORAMIDIC ACID DERIVATIVE;

EID: 0031562483     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(97)00084-7     Document Type: Article
Times cited : (107)

References (45)
  • 28
    • 0029122961 scopus 로고
    • 8. Asymmetric allylations of aldehydes mediated by chiral diamines: Kobayashi, S.; Nishio, K. Tetrahedron Lett. 1995, 36, 6729-6732.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 6729-6732
    • Kobayashi, S.1    Nishio, K.2
  • 32
    • 0011432795 scopus 로고    scopus 로고
    • note
    • w = 0.036).
  • 38
    • 0011473607 scopus 로고
    • Colorado Springs, CO, USA and Fujitsu, Ltd., Tokyo, Japan, note
    • 17. MOPAC 93 Rev. 2 (JCPE P081): Stewart, J.J.P. Stewart Computational Chemistry, Colorado Springs, CO, USA and Fujitsu, Ltd., Tokyo, Japan, 1993. 18. The geometry optimized structures of 4d and 4m, based on X-ray crystallography, were used for the PM-3 calculations.
    • (1993) Stewart Computational Chemistry , vol.18
    • Stewart, J.J.P.1
  • 39
    • 0011477081 scopus 로고    scopus 로고
    • note
    • 19. Conformer A was calculated to account for 69% of all conformer concentrations from 4d at -60°C.
  • 40
    • 0011431580 scopus 로고    scopus 로고
    • note
    • 20. The ratio of conformer B and the stablest conformer at -60°C was calculated to be approximately 49:51.
  • 41
    • 0011439548 scopus 로고    scopus 로고
    • note
    • 21. The stablest conformer obtained from 4m appears not to have sufficient space to form a cyclic chair transition structure with benzaldehyde.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.