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Volumn 68, Issue 14, 2003, Pages 5754-5757

The sulfinyl moiety as an internal nucleophile. 2. Stereoselective synthesis of (-)-galantinic acid via 1,3-asymmetric induction

Author keywords

[No Author keywords available]

Indexed keywords

RACEMIC EPOXIDE;

EID: 0037999777     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo026892y     Document Type: Article
Times cited : (28)

References (28)
  • 13
    • 0038061844 scopus 로고    scopus 로고
    • note
    • 3CN. (equation presented)
  • 14
    • 0038738273 scopus 로고    scopus 로고
    • note
    • The alcohol 9 was transformed into its mandelate ester by reaction with -α-methoxy mandelic acid and found to be homogeneous by comparing it with the ester prepared from racemic 9. The absolute configurations of the product were determined by application of the models for the HKR reaction and by total synthesis.
  • 15
    • 0038061845 scopus 로고    scopus 로고
    • note
    • Attempted kinetic resolution of the epoxide 6, using 0.55 equiv of PhSH in the presence of (R,R)-salen Co(III)OAc catalyst, afforded only racemic product 9.
  • 26
    • 0038738271 scopus 로고    scopus 로고
    • note
    • 1H NMR, which revealed a multiplet at 6 5.1.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.