133789-00-1Relevant academic research and scientific papers
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.
Stereoselective Synthesis of Cis-Substituted Azetidinones from Penicillin: a Formal Total Synthesis of Loracarbef
Deeter, Jack B.,Hall, David A.,Jordan, Christopher L.,Justice, Richard M.,Kinnick, Michael D.,et al.
, p. 3051 - 3054 (2007/10/02)
A new method for the synthesis of chiral azetidinones bearing a carbon-carbon bond at the 4-position is described.The preparation involves a stereoselective alkylation-reduction of a silylated 4-phenylsulfonyl azetidinone.The utility of this method was demonstrated by a formal total synthesis of loracarbef.
