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Volumn 35, Issue 25, 1994, Pages 4419-4422

Asymmetric 13-dipolar cycloaddition of nitrones with ketene acetals catalyzed by chiral oxazaborolidines

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID DERIVATIVE; ESTER DERIVATIVE; ISOQUINOLINE DERIVATIVE;

EID: 0028361611     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)73373-9     Document Type: Article
Times cited : (111)

References (39)
  • 7
    • 0002562810 scopus 로고
    • Asymmetric 1,3-Dipolar Cycloaddition of Cyclic Nitrones to Crotonic Acid Derivatives Bearing Chiral Auxiliaries. Synthesis of Optically Active β-Amino Acids, (+)-Sedridine, and (+)-Hygroline
    • (ref. 2 and 3 cited therein)
    • (1993) Synlett , pp. 395-396
    • Murahashi1    Imada2    Kohno3    Kawakami4
  • 12
    • 0027398063 scopus 로고
    • 2) in the 13-dipolar cycloaddition of nitrones with electron-poor (chiral) dipolarophiles has been reported recently : ref. 2a
    • (1993) Tetrahedron Lett. , vol.34 , pp. 87-90
    • Kanemasa1    Tsuruoka2    Wada3
  • 19
    • 0002555866 scopus 로고
    • Carbon-carbon bond forming reaction assisted by silicon transfer. The reaction between nitrones and ketene silyl acetals.
    • Silyl ketene acetals are known to give silyl group-transfer 1,3-addition reactions with nitrones instead of ordinary 1,3-dipolar cycloadditions
    • (1982) Chemistry Letters , pp. 1787-1790
    • Tomoda1    Takeuchi2    Nomura3
  • 21
    • 37049082002 scopus 로고
    • Ketene silyl acetal chemistry; diastereofacial selectivity of 1,3-addition of chiral nitrones
    • preliminary results on the 1,3-dipolar cycloaddition of several nitrones with enol ethers show that this reaction is strongly catalyzed by chiral oxazaborolidines at room temperature yielding 5-alkoxy-isoxazolidines in high yield (to be published).
    • (1988) Journal of the Chemical Society, Chemical Communications , pp. 761-763
    • Kita1    Tamura2    Itoh3    Kishino4    Miki5    Kohno6    Tamura7
  • 28
    • 84912949041 scopus 로고    scopus 로고
    • 3N). Yields: ca. 80–99%.
  • 39
    • 84912900488 scopus 로고    scopus 로고
    • Financial support by the Innovation Oriented Research Program (IOP) on Catalysis (no.90034) of the Netherlands Ministry of Economic Affairs is gratefully acknowledged.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.