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Volumn 52, Issue 11, 1996, Pages 4079-4094

Asymmetric Diels-Alder reactions employing modified camphor-derived oxazolidin-2-one chiral auxiliaries

Author keywords

[No Author keywords available]

Indexed keywords

2 OXAZOLIDINONE DERIVATIVE; CAMPHOR DERIVATIVE;

EID: 0029881993     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(96)00070-1     Document Type: Article
Times cited : (29)

References (16)
  • 7
    • 0000318952 scopus 로고
    • M. P.
    • We prepared compound 2 from exo-borneol [prepared by L-Selectride reduction of (1R)-camphor] using our nitreno-mediated route (ref. 4) to construct the oxazolidin-2-one ring (G.B. patent application No. 901268.0, filing date 7th July 1990); see Bonner also M. P. and Thornton E. R., J. Am. Chem. Soc., 1991, 113, 1299-1308 for an alternative synthesis from (1R)-(-)-camphorquinone by conversion into the corresponding exo, exo-aminoalcohol followed by cyclocarbamation.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 1299-1308
    • Bonner1    Thornton, E.R.2
  • 11
    • 0028116319 scopus 로고
    • Jauch J, Tetrahedron, 1994, 50, 12903-12912.
    • (1994) Tetrahedron , vol.50 , pp. 12903-12912
    • Jauch, J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.