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Volumn , Issue 11, 1997, Pages 2215-2220

Mukaiyama reactions of a silyl enol ether with heteroatom-substituted β-formyl esters

Author keywords

Aldol reactions; Chelates; Silyl enol ethers; Formyl esters; Lactones

Indexed keywords


EID: 0005215092     PISSN: 09473440     EISSN: None     Source Type: Journal    
DOI: 10.1002/jlac.199719971107     Document Type: Article
Times cited : (14)

References (42)
  • 1
    • 33748739637 scopus 로고
    • Dissertation, Technische Universität Dresden
    • H. Angert, Dissertation, Technische Universität Dresden, 1995.
    • (1995)
    • Angert, H.1
  • 18
    • 33748735481 scopus 로고    scopus 로고
    • note
    • 1H-NMR spectroscopy.
  • 28
    • 33748726902 scopus 로고    scopus 로고
    • note
    • The configurational assignment of 11 is based on NMR arguments as presented in our earlier papers (see ref. [2-5]).
  • 33
    • 33748716001 scopus 로고    scopus 로고
    • note
    • The configurational assignment of the isomers was unequivocally possible by 2D-NOESY-NMR spectra.
  • 34
    • 0001316868 scopus 로고
    • (Eds.: B. M. Trost, I. Fleming), Pergamon Press, Oxford, Chapt. 2.4
    • For Mukaiyama reactions of other benzyloxy substituted aldehydes, see: C. Gennari in Comprehensive Organic Synthesis (Eds.: B. M. Trost, I. Fleming), Pergamon Press, Oxford, 1991, Vol. 2, Chapt. 2.4.
    • (1991) Comprehensive Organic Synthesis , vol.2
    • Gennari, C.1
  • 41
    • 33748735609 scopus 로고    scopus 로고
    • note
    • Unfortunately, we were not able to prepare the corresponding dibenzylamino-protected aldehyde which is a highly promising candidate for stereoselective reactions.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.