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Volumn 131, Issue 9, 2009, Pages 3122-3123

Catalytic enantioselective synthesis of tetrahydrofurans: A dynamic kinetic asymmetric [3 + 2] cycloaddition of racemic cyclopropanes and aldehydes

Author keywords

[No Author keywords available]

Indexed keywords

CHELATION; MAGNESIUM COMPOUNDS; ORGANIC SOLVENTS; PROPANE;

EID: 67749106330     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja809873u     Document Type: Article
Times cited : (267)

References (36)
  • 2
    • 0001796781 scopus 로고
    • For D-A cyclopropane reviews, see: a
    • For D-A cyclopropane reviews, see: (a) Reissig, H.-U. Top. Curr. Chem. 1988, 144, 73-135.
    • (1988) Top. Curr. Chem. , vol.144 , pp. 73-135
    • Reissig, H.-U.1
  • 27
    • 17744393466 scopus 로고    scopus 로고
    • Sibi and coworkers reported an enantioselective synthesis of cis-and trans-tetrahydro-1, 2-oxazines via cycloaddition of racemic D-A cyclopropanes and nitrones, perhaps resulting from enantiodifferentiation after the first irreversible step. See:, For a definition and discussion, see
    • (a) Sibi and coworkers reported an enantioselective synthesis of cis-and trans-tetrahydro-1, 2-oxazines via cycloaddition of racemic D-A cyclopropanes and nitrones, perhaps resulting from enantiodifferentiation after the first irreversible step. See: Sibi, M. P.; Ma, Z.; Jasperse, C. P. J. Am. Chem. Soc. 2005, 127, 5764-5765. For a definition and discussion, see
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 5764-5765
    • Sibi, M.P.1    Ma, Z.2    Jasperse, C.P.3
  • 29
    • 34250782234 scopus 로고    scopus 로고
    • Tang and co-workers reported a simple kinetic resolution of racemic D - A cyclopropanes to access enantioenriched tetrahydro-1, 2-oxazines and cyclopropanes via cycloaddition with nitrones. See
    • Tang and co-workers reported a simple kinetic resolution of racemic D - A cyclopropanes to access enantioenriched tetrahydro-1, 2-oxazines and cyclopropanes via cycloaddition with nitrones. See: Kang, Y.-B.; Sun, X.-L.; Tang, Y. Angew. Chem., Int. Ed. 2007, 46, 3918-3921.
    • (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 3918-3921
    • Kang, Y.-B.1    Sun, X.-L.2    Tang, Y.3
  • 30
    • 33845238277 scopus 로고    scopus 로고
    • For a review of stereoselective THF synthesis, see
    • For a review of stereoselective THF synthesis, see: Wolfe, J. P.; Hay, M. B. Tetrahedron 2007, 63, 261-290.
    • (2007) Tetrahedron. , vol.63 , pp. 261-290
    • Wolfe, J.P.1    Hay, M.B.2
  • 35
    • 84925561605 scopus 로고    scopus 로고
    • 2 complexes as stoichiometric enantioselective promoters, see
    • 2 complexes as stoichiometric enantioselective promoters, see


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.