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Dive into the research topics where Michael J. Castaldi is active.

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Featured researches published by Michael J. Castaldi.


Diagnostic Microbiology and Infectious Disease | 1994

In vitro activity of CP-99,219, a novel 7-(3-azabicyclo[3.1.0]hexyl) naphthyridone antimicrobial

Thomas D. Gootz; Katherine E. Brighty; Marge R. Anderson; Brenda J. Schmieder; Suzanne L. Haskell; Joyce A. Sutcliffe; Michael J. Castaldi; Paul Robert Mcguirk

The in vitro activity of CP-99,219 was compared with that of ciprofloxacin and sparfloxacin against 814 clinical bacterial isolates using a microdilution method with brain-heart infusion broth. CP-99,219 was the most potent agent tested against methicillin-resistant, ciprofloxacin-susceptible staphylocci (minimum inhibitory concentration [MIC]90 < or = 0.25 microgram/ml). CP-99,219 was 32-fold and fourfold more potent than ciprofloxacin and sparfloxacin, respectively, against Streptococcus pneumoniae, including strains resistant to penicillin G and erythromycin (MIC90 < or = 0.25 microgram/ml). CP-99,219 was also the most potent agent tested against S. pyogenes and Enterococcus faecalis (MIC90 < or = 0.5 microgram/ml). The activity of CP-99,219 against Enterobacteriaceae was comparable to that of sparfloxacin, with 90% of Escherichia coli, Enterobacter cloacae, Enterobacter aerogenes, Klebsiella pneumoniae, Citrobacter freundii, C. diversus, Helicobacter pylori, and K. oxytoca being inhibited by < or = 0.5 microgram/ml. Serratia marcescens, Morganella morganii, and Pseudomonas aeruginosa were less susceptible, with MIC90 values to CP-99,219 of 4, 2, and 2 micrograms/ml, respectively. The MIC90 for Bacteroides fragilis was 0.39 microgram/ml for CP-99,219 compared with 12.5 micrograms/ml for ciprofloxacin. CP-99,219 was highly bactericidal at 1 x to 4 x MIC against both Gram-positive and Gram-negative organisms; its activity was similar in nutrient, trypticase soy, and cation-supplemented Mueller-Hinton broths. The spectrum and potency observed with CP-99,219 warrant further testing with this novel quinolone.


Synthetic Communications | 2006

Scalable Process for 4‐(2‐Hydroxy‐2‐methyl)‐ethyl‐benzylamine

John L. Tucker; Michel Couturier; Michael J. Castaldi; Charles K.-F. Chiu; Detlef Gestmann

Abstract The preparation of the title compound has been revisited and improved. Starting from inexpensive cuminonitrile, 4‐(2‐hydroxy‐2‐methyl)‐ethyl‐benzylamine is obtained in a scalable two‐step process with an overall yield of 55%.


Organic Process Research & Development | 2005

Evaluation of kilogram-scale Sonagashira, Suzuki, and Heck coupling routes to oncology candidate CP-724,714

David H. Brown Ripin; Dennis E. Bourassa; Thomas A. Brandt; Michael J. Castaldi; Heather N. Frost; Joel M. Hawkins; Phillip J. Johnson; Stephen S. Massett; Karin Neumann; James Phillips; Jeffery W. Raggon; Peter Robert Rose; Jennifer L. Rutherford; Barbara J. Sitter; A. Morgan Stewart; Michael G. Vetelino; Lulin Wei


Synlett | 2000

Synthesis of (1α,5α,6α)-6-Amino-3-azabicyclo[3.1.0]hexane, a Novel Achiral Diamine

Katherine E. Brighty; Michael J. Castaldi


Archive | 2003

Novel processes and intermediates for preparing triazolo-pyridines

Richard A. Buzon; Michael J. Castaldi; Zhengong Bryan Li; David H. Brown Ripin; Yong Tao


Organic Process Research & Development | 2001

Investigation of Methods for Seven-Membered Ring Synthesis: A Practical Synthesis of 4-Oxo-5,6,7,8-tetrahydro-4H-cyclohepta[b]furan-3-carboxylic Acid

John A. Ragan; Jerry Anthony Murry; Michael J. Castaldi; Alyson Kay Conrad; Brian P. Jones; Bryan Li; Teresa W. Makowski; Ruth E. McDermott; Barb J. Sitter; and Timothy D. White; Gregory R. Young


Organic Process Research & Development | 2003

Synthesis and purification of 6-ethoxy-4-oxo-1,4-dihydro-[1,5]naphthyridine-3-carboxylic acid benzylamide

Justin Beaudin; Dennis E. Bourassa; Paul Bowles; Michael J. Castaldi; Ronald J. Clay; Michel Couturier; Gregory L. Karrick; Teresa W. Makowski; Ruth E. McDermott; Clifford N. Meltz; Morgan Meltz; James Phillips; John A. Ragan; David H. Brown Ripin; Robert A. Singer; John L. Tucker; Lulin Wei


Synthesis | 1998

2,5-Dimethylpyrrole Protection Facilitates Copper(I)-Mediated Methoxylations of Aryl Iodides in the Presence of Anilines

John A. Ragan; Teresa W. Makowski; Michael J. Castaldi; Paul D. Hill


Archive | 2004

Crystal forms of 2-(3-difluoromethyl-5-phenyl-pyrazol-1-yl)-5-methanesulfonyl pyridine

Zheng J. Li; Robert J. Rafka; David H. Brown Ripin; Michael J. Castaldi


Archive | 2000

Polymorphs of a crystalline azo-bicyclo (2,2,2) octan-3-amine citrate and their pharmaceutical compositions

George J. Quallich; Lewin Theophilus Wint; Michael J. Castaldi

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