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Volumn 36, Issue 7, 2007, Pages 826-827

Lewis acid mediated reactions of allyl chalcogenides with ethyl glyoxylate

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EID: 34547230602     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.2007.826     Document Type: Article
Times cited : (5)

References (28)
  • 14
    • 0343778881 scopus 로고    scopus 로고
    • For reviews of [3 + 2] cycloaddition reactions of allylsilanes: a C. E. Masse, J. S. Panek, Chem. Rev. 1995, 95, 1293.
    • For reviews of [3 + 2] cycloaddition reactions of allylsilanes: a) C. E. Masse, J. S. Panek, Chem. Rev. 1995, 95, 1293.
  • 16
    • 34547161216 scopus 로고    scopus 로고
    • For hydrolysis and stereochemistry of 3c and 5a, see Supporting Information, which is available electronically on the CSJ-Journal Web site, http://www.csj.jp/joumals/chem-lett/index.html.
    • For hydrolysis and stereochemistry of 3c and 5a, see Supporting Information, which is available electronically on the CSJ-Journal Web site, http://www.csj.jp/joumals/chem-lett/index.html.
  • 17
    • 0034707974 scopus 로고    scopus 로고
    • Similar stereoselectivities were shown in the reactions of allylic silanes. a G. C. Micalizio, W. R. Roush, Org. Lett. 2000, 2, 461.
    • Similar stereoselectivities were shown in the reactions of allylic silanes. a) G. C. Micalizio, W. R. Roush, Org. Lett. 2000, 2, 461.
  • 26
    • 0342908106 scopus 로고    scopus 로고
    • The cycloaddition reactions of allylic silanes proceeded via synclinal transition states, a J. S. Panek, R. Beresis, J. Org. Chem. 1993, 58, 809.
    • The cycloaddition reactions of allylic silanes proceeded via synclinal transition states, a) J. S. Panek, R. Beresis, J. Org. Chem. 1993, 58, 809.
  • 27
    • 34547152640 scopus 로고    scopus 로고
    • T. Akiyama, K. Ishikawa, S. Ozaki, Chem. Lett. 1994, 627. See also:
    • b) T. Akiyama, K. Ishikawa, S. Ozaki, Chem. Lett. 1994, 627. See also:


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.