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Tetrahedron Letters

Volumn 43, Issue 27, 2002, Pages 4805-4808

Electrolytic partial fluorination of organic compounds. Part 61: The first example of direct α-fluorination of protected α-amino acids

(2) Baba, Daisuke a Fuchigami, Toshio a

a Tokyo Institute of Technology ^* (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA AMINO ACID; N (CARBOETHOXY)METHYLPHTHALIMIDE; ORGANIC COMPOUND; OXAZOLIDINE DERIVATIVE; PYROGLUTAMIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

AMINO ACID ANALYSIS; ARTICLE; CHEMICAL REACTION; CHEMICAL REACTION KINETICS; ELECTROLYSIS; FLUORINATION; PROTECTION;

EID: 0036644138 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(02)00924-3 Document Type: Article

Times cited : (26)

References (20)

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- 2) was passed until the starting material was consumed. After the electrolysis, the resulting electrolytic solution was passed through a short column chromatography on silica gel using ethyl acetate to remove the fluoride salt. The eluent was evaporated under vacuum and the residue was purified by column chromatography on silica gel (hexane to hexane/AcOEt).

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.