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Volumn 10, Issue 28, 2012, Pages 5431-5442

Stereocontrolled synthesis of carbocyclic compounds with a quaternary carbon atom based on SN2′ alkylation of γ,δ-epoxy- α,β-unsaturated ketones

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL MOIETIES; ALDOL CONDENSATION; ALKYLATION REACTIONS; CARBOCYCLIC RINGS; COMPLEX MOLECULES; CYCLIC KETONES; EPOXY ALDEHYDES; QUATERNARY CARBON; STEREO-SELECTIVE; STEREOCONTROLLED SYNTHESIS; STEREOGENIC CENTERS; STEREOSELECTIVE CONSTRUCTION; STEREOSELECTIVE FORMATION; SUBSTITUTION PRODUCTS; UNSATURATED KETONES;

EID: 84863609356     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c2ob25719j     Document Type: Article
Times cited : (4)

References (38)
  • 29
    • 0004219714 scopus 로고    scopus 로고
    • M. Schlosser, John Wiley & Sons Ltd., New York, 2nd edn, 579-664 Optically active epoxide (+)- was prepared from the corresponding optically active epoxy alcohol (+)- 26 (92% ee), which was easily accessible through the Katsuki-Sharpless asymmetric epoxidation.: Enantiomeric excesses of (-)- 17a-anti and (+)- 17a-syn were determined by HPLC analysis with a chiral column (see ESI).
    • E. Nakamura, in Organometallics in Synthesis: A Manual, ed., M. Schlosser, John Wiley & Sons Ltd., New York, 2nd edn, 2002, pp. 579-664
    • (2002) Organometallics in Synthesis: A Manual , vol.16
    • Nakamura, E.1
  • 30
    • 0026016046 scopus 로고
    • 2 and vinylmagnesium bromide and was used directly without removal of magnesium salts; see
    • B. B. Kikani J. R. McKee M. Zanger Synthesis 1991 176
    • (1991) Synthesis , pp. 176
    • Kikani, B.B.1    McKee, J.R.2    Zanger, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.