119892-46-5Relevant academic research and scientific papers
Use of an iodonium ylide in the synthesis of p-nitrobenzyl (6R, 7S) 3-hydroxy-8-oxo-7-phenoxyacetamido-1-azabicyclo[4.2.0] octa-2-ene-2-carboxylate
Vaid, Radhe K.,Hopkins, Thomas E.
, p. 6981 - 6984 (1997)
p-Nitrobenzyl (6R,7S)-3-hydroxy-8-oxo-7-phenoxyacetamido-1-azabicyclo [4.2.0]octa-2-ene-2-carboxyate (6) was synthesized utilizing rhodium(II)- or acid-catalyzed cyclization of iodonium ylide (5). The iodonium ylide (5) was easily prepared from the corres
Halide-terminated N-acyliminium ion-alkyne cyclizations: A new construction of carbacephem antibiotics
Metais, Eric,Overman, Larry E.,Rodriguez, Maria Ines,Stearns, Brian A.
, p. 9210 - 9216 (2007/10/03)
A series of 4-(3-alkynyl)azetidinones 13 was prepared from 4- (phenylsulfonyl)azetidine-2-one (9) and isopropyl glyoxylate hydrate. The 3- pentynyl (13a) and 4-phenyl-3-butynyl (13b) azetidinone acetates underwent 6- exo cyclization when treated with 3 equity of SnCl4 at 0 °C to provide 3- (1-chloroalkylidene)carbacephems 15a (65%) and 15b (33%) respectively. In contrast, the 3-butynyl (13d) and 4-(trimethylsilyl)-3-butynyl (13c) azetidinone acetates underwent 7-endo cyclization under similar conditions to give 1-azabicyclo[5.2.0]nonenes 14a (11%) and 14b (71%), respectively. Beginning with penicillin degradation product 18, the more elaborate 3- pentynyl azetidinone cyclization substrate 27 was prepared in seven steps. Exposure to 27 to 3 equiv of SnCl4 in CH2Cl2 at 0 °C for 6 h, followed by allowing the reaction mixture to warm to rt, provided the desired 3-(1- chloroethylidene)carbacephem 28 in 60% yield and high (>99%) enantiometric purity. Cleavage of the chloroethylidene group of 28 with ozone gave 3- hydroxy carbacephem 29 in 77% yield. Since this intermediate has been converted in three steps to loracarbef (3), a new formal total synthesis of this carbacephem antibiotic was concluded.
Synthesis of carbacephem antibiotics: Synthesis via Dieckmann reaction using phenyl esters to direct the regioselectivity of the cyclization
Jackson, Bill G.,Gardner, John P.,Heath, Perry C.
, p. 6317 - 6320 (2007/10/02)
β-Ketoesters useful for elaboration to carbacephems were synthesized from a variety of enantiomerically pure diesters. Use of phenyl esters to direct the regioselectivity was demonstrated.
AN ENANTIOSELECTIVE SYNTHESIS OF LORACARBEF (LY163892/KT3777)
Bodurow, C. C.,Boyer, B. D.,Brennan, J.,Bunnell, C. A.,Burks, J. E.,et al.
, p. 2321 - 2324 (2007/10/02)
An enantioselective synthesis of the new, orally absorbable, totally synthetic β-lactam antibiotic, loracarbef(LY163892/KT3777) is described.
