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Volumn 37, Issue 46, 1996, Pages 8341-8344

Ylide-mediated bis-cyclopropane formation: A reversal in substrate-mediated facial selectivity

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPROPANE DERIVATIVE;

EID: 0030580306     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)01907-7     Document Type: Article
Times cited : (15)

References (40)
  • 27
    • 0011873383 scopus 로고
    • Undergraduate Senior Thesis, University of New Hampshire
    • 10 Hanna, M. R.; Undergraduate Senior Thesis, University of New Hampshire, 1993. The most likely reason for the greater yields when using the t-butyl ester is the lability of the methyl and ethyl ester to residual sodium hydroxide.
    • (1993)
    • Hanna, M.R.1
  • 30
    • 0011884264 scopus 로고    scopus 로고
    • note
    • 4, filtered, and concentrated. The crude product was stirred in THF at -78 °C while 6 equiv. of DIBAL-H in toluene was added. The reaction was quenched at room temperature by the addition of 2N NaOH, dried with MgSO4, filtered, and concentrated. The crude oil was purified by chromatography on silica.
  • 31
    • 85136568202 scopus 로고    scopus 로고
    • manuscript submitted for publication
    • 13C resonances. No evidence was observed for the formation of ciscyclopropanes. Theberge, C. R.; Verbicky, C. A.; Zercher, C. K., manuscript submitted for publication;
    • Theberge, C.R.1    Verbicky, C.A.2    Zercher, C.K.3
  • 35
    • 0011834805 scopus 로고
    • Z. Rappaport, Ed., John Wiley & Sons; New York
    • d) W. Runge in "The Chemistry of the Cyclopropyl Group", Part 1; Z. Rappaport, Ed., John Wiley & Sons; New York, 1987, p 66.
    • (1987) The Chemistry of the Cyclopropyl Group , vol.66 , Issue.PART 1
    • Runge, W.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.