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Volumn 346, Issue 9-10, 2004, Pages 1111-1115

Catalysis of the Hajos-Parrish-Eder-Sauer-Wiechert reaction by cis- and trans-4,5-methanoprolines: Sensitivity of proline catalysis to pyrrolidine ring conformation

Author keywords

Aldol; Asymmetric catalysis; Cyclization; Hybrid density functional theory; Organic catalysis; Proline

Indexed keywords

AMINE; PROLINE DERIVATIVE; PYRROLIDINE DERIVATIVE;

EID: 5144225978     PISSN: 16154150     EISSN: None     Source Type: Journal    
DOI: 10.1002/adsc.200404127     Document Type: Article
Times cited : (66)

References (48)
  • 1
    • 5144229644 scopus 로고    scopus 로고
    • German Patent DE 2,102,623, 1971
    • a) Z. G. Hajos, D. R. Parrish, German Patent DE 2,102,623, 1971;
    • Hajos, Z.G.1    Parrish, D.R.2
  • 37
    • 5144230434 scopus 로고    scopus 로고
    • note
    • 298, were computed at the same level of theory for the gas phase. The electronic energies were taken from a single point at the B3LYP/6-311+G(2df, p) level of theory. Stereoselectivities were predicted using transition state theory;
  • 43
    • 5144225743 scopus 로고    scopus 로고
    • note
    • σ.
  • 45
    • 5144231987 scopus 로고    scopus 로고
    • note
    • δ- electrostatic interactions, as described in reference for the Hajos-Parrish-Eder-Sauer-Wiechert reaction;
  • 47
    • 5144224092 scopus 로고    scopus 로고
    • [6]
    • [6];
  • 48
    • 1942437543 scopus 로고    scopus 로고
    • New mechanistic studies on the proline-catalyzed aldol reaction
    • b) "New mechanistic studies on the proline-catalyzed aldol reaction", B. List, L. Hoang, H. J. Martin. PNAS 2004, 101, 5839.
    • (2004) PNAS , vol.101 , pp. 5839
    • List, B.1    Hoang, L.2    Martin, H.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.