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Volumn 16, Issue 29, 2010, Pages 8605-8609

Concise asymmetric synthesis of fully substituted isoxazoline-N-Oxide through lewis base catalyzed nitroalkene activation

Author keywords

Asymmetric synthesis; Clausenamide; Enantioselectivity; Isoxazoline N oxides; Lewis bases

Indexed keywords

ASYMMETRIC SYNTHESIS; GRAM-SCALE SYNTHESIS; INTERMOLECULAR CONDENSATION; ISOXAZOLINES; LEWIS BASE; LEWIS BASIS; N-OXIDES; SECONDARY AMINES; SULFUR YLIDES;

EID: 77955124333     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201001237     Document Type: Article
Times cited : (58)

References (65)
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    • See the Supporting Information for the detailed screening conditions
    • See the Supporting Information for the detailed screening conditions.
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    • The detailed mechanistic study of the interaction between chiral secondary amine Lewis base and the nitro alkene or the intermediate is currently under investigation
    • The detailed mechanistic study of the interaction between chiral secondary amine Lewis base and the nitro alkene or the intermediate is currently under investigation.
  • 51
    • 51649105642 scopus 로고    scopus 로고
    • for related studies in asymmetric chiral sulfur ylide auxiliaries, see: b) X.-L. Sun, Y. Tang, Acc. Chem Res. 2008, 41, 937-948;
    • (2008) Acc. Chem Res. , vol.41 , pp. 937-948
    • Sun, X.-L.1    Tang, Y.2
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    • The single-crystal X-ray structure of 6a revealed the formation of a hydrogen bond for improved stereochemistry control. (Figure Presented)
    • The single-crystal X-ray structure of 6a revealed the formation of a hydrogen bond for improved stereochemistry control. (Figure Presented)
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    • For the synthesis of Clausenamide
    • c) L. Xu, S.L. Liu, J. T. Zhang, Chirality 2005, 17, 239-244. For the synthesis of Clausenamide:
    • (2005) Chirality , vol.17 , pp. 239-244
    • Xu, L.1    Liu, S.L.2    Zhang, J.T.3
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    • 2D NMR studies and the X-ray structure for 8e are provided in the Supporting Information, and indicated the all-cis configuration of the γ-lectam
    • 2D NMR studies and the X-ray structure for 8e are provided in the Supporting Information, and indicated the all-cis configuration of the γ-lectam.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.