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Volumn 36, Issue 34, 1995, Pages 6079-6082

Diastereoselective synthesis of trans-1,2-disubstituted cyclopropanols from homoallyl or bis-homoallyl esters via tandem intramolecular nucleophilic acyl substitution and intramolecular carbonyl addition reactions mediated by Ti(OPr-i)4 / 2 i-PrMgBr reagent

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPROPANE DERIVATIVE; CYCLOPROPANOL DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0029161631     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(95)01208-Y     Document Type: Article
Times cited : (92)

References (19)
  • 7
    • 84914019723 scopus 로고    scopus 로고
    • Urabe, H.; Hata, T.; Sato, F. Tetrahedron Lett. in press.
  • 15
    • 84914019722 scopus 로고    scopus 로고
    • Kasatkin, A.; Okamoto, S.; Sato, F. Tetrahedron Lett. submitted for publication.
  • 16
    • 84914019721 scopus 로고    scopus 로고
    • Allyl esters react with 1 to afford allyltitanium compounds, see ref. 3a.
  • 17
    • 84989132147 scopus 로고
    • Etudes par la RMN du carbone-13 de quelques dérivés cyclopropaniques: Déplacements chimiques et paramètres structuraux
    • 2- or CH-fragments attached to C-1 position were observed 5–6 ppm upfield compared to those of corresponding trans-isomers, see:
    • (1976) Organic Magnetic Resonance , vol.8 , pp. 611
    • Monti1    Faure2    Vincent3
  • 19
    • 84914019720 scopus 로고    scopus 로고
    • f 0.17) in 93% total yield.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.