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Dive into the research topics where Carl Deamicis is active.

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Featured researches published by Carl Deamicis.


Journal of Computer-aided Molecular Design | 2008

Neural network-based QSAR and insecticide discovery: spinetoram

Thomas C. Sparks; Gary D. Crouse; James Edwin Dripps; Peter Biagio Anzeveno; Jacek G. Martynow; Carl Deamicis; James M. Gifford

Improvements in the efficacy and spectrum of the spinosyns, novel fermentation derived insecticide, has long been a goal within Dow AgroSciences. As large and complex fermentation products identifying specific modifications to the spinosyns likely to result in improved activity was a difficult process, since most modifications decreased the activity. A variety of approaches were investigated to identify new synthetic directions for the spinosyn chemistry including several explorations of the quantitative structure activity relationships (QSAR) of spinosyns, which initially were unsuccessful. However, application of artificial neural networks (ANN) to the spinosyn QSAR problem identified new directions for improved activity in the chemistry, which subsequent synthesis and testing confirmed. The ANN-based analogs coupled with other information on substitution effects resulting from spinosyn structure activity relationships lead to the discovery of spinetoram (XDE-175). Launched in late 2007, spinetoram provides both improved efficacy and an expanded spectrum while maintaining the exceptional environmental and toxicological profile already established for the spinosyn chemistry.


Journal of Chromatography A | 2011

Comparison of preparative reversed phase liquid chromatography and countercurrent chromatography for the kilogram scale purification of crude spinetoram insecticide

Carl Deamicis; Neil A. Edwards; Michael B. Giles; Guy Harris; Peter Hewitson; Lee Janaway; Svetlana Ignatova

Reversed phase HPLC (RP-HPLC) and high performance countercurrent chromatography (HPCCC) were compared for the pilot scale purification of two semi-synthetic spinosyns, spinetoram-J and spinetoram-L, the major components of the commercial insecticide spinetoram. Two, independently performed, 1 kg, purification campaigns were compared. Each method resulted in the isolation of both components at a purity of >97% and yields for spinetoram-J and spinetoram-L of >93% and ≥ 63% of theoretical, respectively. The HPCCC process produced a 2-fold higher throughput and consumed approximately 70% less solvent than preparative scale RP-HPLC, the volume of product containing fractions from HPCCC amounted to 7% of that produced by HPLC and so required much less post-run processing.


Pest Management Science | 2011

Synthesis of new compounds related to the commercial fungicide tricyclazole.

Jesse L. Balcer; Carl Deamicis; Peter L. Johnson; Jerzy Klosin; Gregory T. Whiteker; C Srinivas Rao; Donghua Dai

BACKGROUND Tricyclazole is a commercial fungicide used to control rice blast. As part of re-registration activities, samples of metabolites and process impurities are required. In addition, isotopically labeled tricyclazole samples are also required. RESULTS Four new compounds related to tricyclazole are reported. An isotopically labeled sample of tricyclazole was prepared that contained two (15)N atoms and one (13)C atom. Radiolabeled tricyclazole with (14)C at the triazole C3 position was also synthesized. A new process impurity in technical tricyclazole was identified and synthesized. A new metabolite of tricyclazole was identified, independently synthesized and characterized by X-ray crystallography. CONCLUSION A previously unreported metabolite of tricyclazole has been identified and structurally characterized. In addition, a new process impurity has been identified by independent synthesis. Identification of these new compounds has facilitated the continued registration of this important fungicide.


Archive | 2014

Pesticidal compositions and processes related thereto

Maurice C. H. Yap; Ann M. Buysse; Daniel Knueppel; Yu Zhang; Negar Garizi; Noormohamed M. Niyaz; Christian T. Lowe; Ricky Hunter; Tony K. Trullinger; David A. Demeter; Dan Pernich; Carl Deamicis; Ronald Ross; Timothy C. Johnson


Archive | 1996

Synthetic modification of Spinosyn compounds

Carl Deamicis; Peter Biagio Anzeveno; Jacek G. Martynow; Kevin L. McLaren; Frederick Richard Green; Thomas C. Sparks; Herbert A. Kirst; Lawrence Camillo Creemer; Thomas V. Worden; Joe Raymond Schoonover; James M. Gifford; Christopher J. Hatton; Vidyadhar B. Hegde; Gary D. Crouse; Brian R. Thoreen; Michael John Ricks


Archive | 1997

Physical and Biological Properties of the Spinosyns: Novel Macrolide Pest-Control Agents from Fermentation

Carl Deamicis; James Edwin Dripps; Christopher J. Hatton; Laura L. Karr


Pesticide Chemistry and Bioscience#R##N#The Food-Environment Challenge | 1999

Chemistry and Insecticidal Activity of the Spinosyns

Gary D. Crouse; Tom Sparks; Carl Deamicis; Herbert A. Kirst; Jacek G. Martynow; Lawrence Camillo Creemer; Thomas V. Worden; Peter Biagio Anzeveno


Archive | 2002

Reductive cleavage of the exocyclic ester of uk-2a or its derivatives and products formed therefrom

Kevin G. Meyer; Normohammed Mohamed Niyaz; Carl Deamicis; Richard B. Rogers


Archive | 2002

Process to produce derivatives from uk-2a derivatives

Noormohamed M. Niyaz; Carl Deamicis; Richard B. Rogers; Kevin G. Meyer; William H. Dent; Peter Biagio Anzeveno


Archive | 2014

Processes for the preparation of pesticidal compounds

Qiang Yang; Beth Lorsbach; Gary A. Roth; Noormohamed M. Niyaz; Jeffrey Nissen; Ronald Ross; Gregory T. Whiteker; Carl Deamicis; Kaitlyn Gray; Yu Zhang

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