Electrooxidative N-halogenation of 2-azetidinone derivatives

Electrochemistry

Volumn 74, Issue 8, 2006, Pages 656-658

  Tanaka, Hideo ^a   Arai, Shin Ya ^a   Ishitobi, Yoshinori ^a   Kuroboshi, Manabu ^a   Torii, Sigeru ^b  

^a OKAYAMA UNIVERSITY   (Japan)

^b Institute of Creative Chemistry Co   (Japan)

Author keywords

Azetidinone; Electrooxidation; N Halogenation; Lactam Antibiotics

Indexed keywords

DERIVATIVES; ELECTROCHEMISTRY; ELECTROLYSIS; HALOGENATION; METHANOL; OXIDATION; SUBSTITUTION REACTIONS;

AZETIDINONE; ELECTROOXIDATION; N-HALOGENATION; Β-LACTAM ANTIBIOTICS;

KETONES;

EID: 33748990293     PISSN: 13443542     EISSN: None     Source Type: Journal    
DOI: 10.5796/electrochemistry.74.656     Document Type: Article

References (7)

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5. G. Cainelli, P. Galletti, and D. Giacomini, Tetrahedron Lett., 39, 7779 (1998).
6. A similar electrolysis system was employed for C(4)-acetoxylation of non-substituted 2-azetidinone. M. Mori, K. Kagechika, K. Tohjima, and M. Shibasaki, Tetrahedron Lett., 29, 1409 (1988).
7. - would remain in the electrolysis media to shift the equilibrium to the left hand side.