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Volumn 14, Issue 30, 2008, Pages 9131-9134

Unprecedented consecutive, competitive nucleophilic addition to construct densely functionalized propargylic alcohols

Author keywords

Cyclopropanone; Nucleophilic addition; Propargylic alcohol; Tandem reactions

Indexed keywords

ACETYLENE; ALDEHYDES; HEXANE; HYDROCARBONS; LITHIUM; PORT TERMINALS;

EID: 55049138291     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200801452     Document Type: Article
Times cited : (10)

References (30)
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    • Some reports on the organo- or enzymatic-catalyzed reactions of acetaldehyde: a) S. E. Denmark T. Bui. J. Org. Chem. 2005, 70, 10190;
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    • A review for tandem reaction: P. J. Parsons, C. S. Penkett, A. J. Shell, Chem. Rev. 1996, 96, 195.
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    • a = 26-28); F. G. Bordwell. Acc. Chem. Res. 1988, 21, 456.
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    • Some examples to determine the relationship between the basicity and the nucleophilicity of the carbonions: a D. Farah, T. J. Karol, H. G. Kuivila, Organometallics 1985, 4, 662;
    • Some examples to determine the relationship between the basicity and the nucleophilicity of the carbonions: a) D. Farah, T. J. Karol, H. G. Kuivila, Organometallics 1985, 4, 662;
  • 24
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    • Optimization of the reaction conditions is summarized in the Supporting Information
    • Optimization of the reaction conditions is summarized in the Supporting Information.
  • 25
    • 55049112244 scopus 로고    scopus 로고
    • The 1.3-syn dihydroxy stereochemistry of the product 9aa (major isomer in 9a) were deduced from the NOE correlation spectrum of 1,3-dioxane derivative of 9aa, see the Supporting Information for the details.
    • The "1.3-syn dihydroxy" stereochemistry of the product 9aa (major isomer in 9a) were deduced from the NOE correlation spectrum of 1,3-dioxane derivative of 9aa, see the Supporting Information for the details.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.