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Volumn 30, Issue 3, 1989, Pages 309-312

Stereoselective cyclization of α-alkoxyallylstannane alkynals and their Co-complexes. A new route to cyclododecyne-1,2-diol derivatives

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Indexed keywords


EID: 0013532890     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)95187-6     Document Type: Article
Times cited : (29)

References (15)
  • 9
    • 84918596911 scopus 로고    scopus 로고
    • The Multiconformer submode of Clark Still's program MacroModel was used. The five lowest energy conformers of the trans-diol 12 with energies of 16.8, 23.0, 24.8, 25.0 and 25.4 Kj have essentially the identical local conformation at C1-C4. The same is true for the cis-diol 16 with energies of 16.2, 23.5, 23.6, 23.8 and 24.2 Kj. Only the lowest energy conformers are shown in Figure 1. Coupling constants were obtained on the calculated structures through the Analysis submode of MacroModel.
  • 10
    • 85077634689 scopus 로고
    • The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products
    • (1981) Synthesis , pp. 1
    • Mitsunobu1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.