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Volumn 74, Issue 8, 2006, Pages 645-648

Electrochemical oxidation of L-prolinol derivative protected with 1-alkoxy-2,2,2-trifluoroethyl group

Author keywords

Electrochemical Oxidation; Enantiomerically Pure Amino Compound; New Protecting Group; Prolinol

Indexed keywords

DERIVATIVES; ELECTROCHEMISTRY; OXIDATION; REACTION KINETICS;

EID: 33749005924     PISSN: 13443542     EISSN: None     Source Type: Journal    
DOI: 10.5796/electrochemistry.74.645     Document Type: Article
Times cited : (12)

References (14)
  • 6
    • 0000705321 scopus 로고
    • Org. Synth. Coll. Vol. VII, 307 (1990).
    • (1990) Org. Synth. Coll. , vol.7 , pp. 307
  • 7
    • 85039330028 scopus 로고    scopus 로고
    • note
    • It was difficult to isolate 5a since a small amount of unidentified impurities always contaminated 5a. A pos sibility that the impurities involved isomers 5a' and 5a" can not be denied.
  • 8
    • 85039329306 scopus 로고    scopus 로고
    • note
    • Differences of heat of formation calculated by MOPAC PM3 between cis and trans isomers 5a and 5a' and between cis and trans isomers 5b and 5b' were 1.97 and 3.43 kcal/mol, respectively.
  • 11
    • 85039342109 scopus 로고    scopus 로고
    • note
    • The regioselectivity in electrochemical α-methoxylation of bicyclic amine derivatives is on an interesting subject to be explored.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.