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Volumn , Issue 19, 2000, Pages 3325-3334

Dihydroisoquinolinium salts: Catalysts for asymmetric epoxidation

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSTS; HYDROGEN PEROXIDE; OLEFINS; OXIDATION; PORPHYRINS; REACTION KINETICS; SYNTHESIS (CHEMICAL);

EID: 0034619273     PISSN: 14704358     EISSN: None     Source Type: Journal    
DOI: 10.1039/b002156n     Document Type: Article
Times cited : (60)

References (124)
  • 109
    • 33645920774 scopus 로고    scopus 로고
    • Amines for entries c and j were kindly provided by Glaxo-Wellcome
    • Amines for entries c and j were kindly provided by Glaxo-Wellcome.
  • 110
    • 33645938412 scopus 로고    scopus 로고
    • note
    • 3).
  • 111
    • 33645954702 scopus 로고    scopus 로고
    • Absolute configuration of major enantiomer of product. Absolute configurations were assigned by comparison of the sign of optical rotation with literature values
    • Absolute configuration of major enantiomer of product. Absolute configurations were assigned by comparison of the sign of optical rotation with literature values.
  • 112
    • 33645907326 scopus 로고    scopus 로고
    • This figure differs from that reported in our communication (see ref. 31)
    • This figure differs from that reported in our communication (see ref. 31).
  • 113
    • 33645930764 scopus 로고    scopus 로고
    • In contrast to our earlier report (see rEf. 31) the epoxide is in this case formed in the reaction mixture with 20% ee; a fractional crystallization occurs when using our standard work-up, resulting in isolation of the epoxide with up to 63% ee
    • In contrast to our earlier report (see rEf. 31) the epoxide is in this case formed in the reaction mixture with 20% ee; a fractional crystallization occurs when using our standard work-up, resulting in isolation of the epoxide with up to 63% ee.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.