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Volumn 12, Issue 8, 2010, Pages 1660-1663

Asymmetric acid-catalyzed meerwein-ponndorf-verley-aldol reactions of enolizable aldehydes

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; TRIFLUOROACETIC ACID;

EID: 77951200630     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol100093u     Document Type: Article
Times cited : (16)

References (52)
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    • For reviews, see
    • For reviews, see
  • 44
    • 0035926307 scopus 로고    scopus 로고
    • 4 but without any stereoselectivity, see
    • 4 but without any stereoselectivity, see: Aremo, N.; Hase, T. Tetrahedron Lett. 2001, 42, 3637
    • (2001) Tetrahedron Lett. , vol.42 , pp. 3637
    • Aremo, N.1    Hase, T.2
  • 45
    • 33846117174 scopus 로고    scopus 로고
    • For a Meewein-Ponndorf-etherification process, see
    • For a Meewein-Ponndorf-etherification process, see: Corma, A.; Renz, M. Angew. Chem. Int. Ed 2007, 46, 298
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 298
    • Corma, A.1    Renz, M.2
  • 46
    • 0005228367 scopus 로고
    • For rate enhancement of MVP reactions in the presence of protonic acids, see
    • For rate enhancement of MVP reactions in the presence of protonic acids, see: Kow, R.; Nygren, R.; Rathke, M. W. J. Org. Chem. 1977, 42, 826
    • (1977) J. Org. Chem. , vol.42 , pp. 826
    • Kow, R.1    Nygren, R.2    Rathke, M.W.3
  • 48
    • 77951195342 scopus 로고    scopus 로고
    • For optimization of deployment of protonic acids in these reactions see ref 16.
    • For optimization of deployment of protonic acids in these reactions see ref 16.
  • 50
    • 33845693536 scopus 로고    scopus 로고
    • For similar experiments but without any stereoselection, see
    • For similar experiments but without any stereoselection, see: Kamitanaka, T.; Matsuda, T.; Harada, T. Tetrahedron 2007, 63, 1429
    • (2007) Tetrahedron , vol.63 , pp. 1429
    • Kamitanaka, T.1    Matsuda, T.2    Harada, T.3
  • 51
    • 77951160350 scopus 로고    scopus 로고
    • See the Supporting Information.
    • See the Supporting Information.
  • 52
    • 77951173891 scopus 로고    scopus 로고
    • Application of other primary alcohols such as propanol or benzylic alcohol yielded a more complex reaction mixture.
    • Application of other primary alcohols such as propanol or benzylic alcohol yielded a more complex reaction mixture.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.