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Volumn 8, Issue 20, 2006, Pages 4509-4511

Asymmetric multicomponent reactions: Diastereoselective synthesis of substituted pyrrolidines and prolines

Author keywords

[No Author keywords available]

Indexed keywords

PROLINE; PYRROLIDINE DERIVATIVE;

EID: 33750060464     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol061672i     Document Type: Article
Times cited : (19)

References (28)
  • 22
    • 0026600531 scopus 로고
    • Phenyldihydrofuran was prepared using asymmetric Heck reactions in optically enriched form, see: (a) Ozawa, F.; Kubo, A.; Hayashi, T. Tetrahedron Lett. 1992, 33, 1485.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 1485
    • Ozawa, F.1    Kubo, A.2    Hayashi, T.3
  • 24
    • 33750056571 scopus 로고    scopus 로고
    • note
    • Optical purity of 5-phenyl dihydrofuran was 88% ee.
  • 25
    • 33750076553 scopus 로고    scopus 로고
    • note
    • 3, Z = 4; Mo Kα radiation (λ = 0.71073 Å, T = 150 K), R1 = 0.045, wR2 = 0.076 (I > 2σ(I)); R1 = 0.081, wR2 = 0.089 (all data). Crystallographic data has been deposited with the Cambridge Crystallographic Data Center (deposition no. 611303). These data can be obtained free of charge via the Internet at www.ccdc.cam.ac.uk/data_request/cif, by email to data_request@ccdc.cam.ac.uk, or by contacting The Cambridge Crystallographic Data Centre, 12, Union Road, Cambridge CB2 1EZ, U.K.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.