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William Joseph Dubay, 581761 Summer Cloud Ct, Folsom, CA 95630

William Dubay Phones & Addresses

1761 Summer Cloud Ct, Folsom, CA 95630    916-2938667   

314 Eagle St, South Haven, MI 49090    269-6391829    616-6391829   

Troy, MI   

Bloomington, IN   

Lexington, SC   

Sacramento, CA   

PO Box 6192, Folsom, CA 95763    269-6391829   

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William Joseph Dubay

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Work

Company: Ampac fine chemicals Sep 2006 Position: Vp, research and development

Education

Degree: Doctorates School / High School: Indiana University Bloomington 1994 to 1995 Specialities: Organic Chemistry

Skills

R&D • Technology Transfer • Chemistry • Organic Synthesis • Organic Chemistry • Pharmaceutical Industry • Gmp • Chromatography • Validation • Biotechnology • Process Simulation • Program Management • Research and Development • Purification • Manufacturing • Lifesciences • Polymers

Industries

Pharmaceuticals

Mentions for William Joseph Dubay

William Dubay resumes & CV records

Resumes

William Dubay Photo 20

Vp, Research And Development

Location:
Sacramento, CA
Industry:
Pharmaceuticals
Work:
Ampac Fine Chemicals
Vp, Research and Development
Dsm Aug 2002 - Sep 2006
R and D Manager, Custom Manufacturing Fermentation
Catalytica Pharmaceuticals Sep 2000 - Dec 2002
Project Manager
Education:
Indiana University Bloomington 1994 - 1995
Doctorates, Organic Chemistry
University of South Carolina 1989 - 1994
Doctorates, Doctor of Philosophy, Organic Chemistry
Skills:
R&D, Technology Transfer, Chemistry, Organic Synthesis, Organic Chemistry, Pharmaceutical Industry, Gmp, Chromatography, Validation, Biotechnology, Process Simulation, Program Management, Research and Development, Purification, Manufacturing, Lifesciences, Polymers

Publications & IP owners

Wikipedia

William Dubay Photo 21

William Dubay

William DuBay (born 1934) was a U.S. Catholic priest and social activist whose reform activities and suspension from the priesthood created controversy in the
William Dubay Photo 22

Bill Dubay

William Bryan "Bill" DuBay (January 11, 1948 April 15, 2010), whose work sometimes appeared under the pseudonyms Will Richardson and Dube, was an

Us Patents

Reduction Of Aldehydes And Ketones To Alcohols

US Patent:
2013009, Apr 18, 2013
Filed:
Nov 12, 2010
Appl. No.:
13/509580
Inventors:
Charles L. Liotta - Atlanta GA, US
Pamela Pollet - Atlanta GA, US
Kristen Kitagawa Fisher - Sammamish WA, US
William Dubay - Folsom CA, US
Joy Stringer - Folsom CA, US
Assignee:
GEORGIA TECH RESEARCH CORPORATION - Atlanta GA
AMERICAN PACIFIC CORPORATION - Las Vegas NV
International Classification:
C07C 269/06
C07C 29/14
C07C 29/143
C07D 209/48
C07C 231/12
US Classification:
548479, 560 29, 548478, 564213, 564212, 568814
Abstract:
The embodiments described herein provide a reduction of an aldehyde or a ketone, such as a Meerwein-Ponnorf-Verley (MPV) reaction of an aldehyde or ketone. In some embodiments, the reaction occurs in the presence of Al[OC(CH)]. In some embodiments, the reaction occurs in the presence of an aprotic solvent. In some embodiments, the aldehyde or ketone is an amino aldehyde or an amino ketone wherein the amine is group is protected such that the nitrogen of the amine has no proton. Other embodiments related to compositions and compounds related to the reduction reaction, or to the preparation or use of the aldehyde, the ketone, or the resulting alcohol.

Compounds And Methods For Preparing Substituted 3-(1-Amino-2-Methylpentane-3-Yl)Phenyl Compounds

US Patent:
2014035, Nov 27, 2014
Filed:
May 24, 2013
Appl. No.:
13/902296
Inventors:
- Rancho Cordova CA, US
Olivier DAPREMONT - Cameron Park CA, US
Patrick BERGET - Sacramento CA, US
Ali SULEMAN - Folsom CA, US
William DUBAY - Folsom CA, US
Jeffrey D. BUTLER - Folsom CA, US
International Classification:
C07C 253/30
C07C 215/54
C07C 213/02
C07C 255/36
C07C 255/37
US Classification:
558375, 558401, 564374, 564383
Abstract:
Compounds and methods for preparing substituted 3-(1-amino-2-methylpentane-3-yl)phenyl compounds from an isomerically pure starting material are described. In particular, methods of preparing a 3-(1-(dimethylamino)-2-methylpentane-3-yl)phenol as a substantially optically pure (R,R) stereoisomer are described. Using a method of the present invention, only the (R,R) and (S,S) stereoisomers of the target compound are produced, increasing the yield and stereoselectivity of the desired (R,R) stereoisomer.

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