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Eric R Evitt

from Mountain View, CA
Age ~71
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Also known as:
Eric Te Evitt
Phone and address:
1913 Jardin Dr, Mountain View, CA 94040
(650) 949-2220
Related to:
Marie Evitt, 90M Evitt, 71Gisela C Evitt, 96Emily F Evitt, 41William R EvittMark W Evitt, 42David P Evitt, 39Mark Evitt, 39Marie F Evipp, 71Gisela C Evitt
Connected to:
Joel O Evitt, 63Sandra K Evitt, 63Scott W Evitt, 72Betty L Evitts, 97Daniel W Evitts, 51Dorothy H Evitts, 106Margo P Evitts, 78Nadine Evitts, 97Paul E Evitts, 72Eric T Evje, 57

Eric Evitt Phones & Addresses

  • 1913 Jardin Dr, Mountain View, CA 94040 (650) 949-2220 (650) 949-2271
  • Saratoga, CA
  • Walnut Creek, CA
  • Palo Alto, CA

Work

Company: Wilson sonsini goodrich & rosati May 2017 Position: Patent agent

Education

School / High School: Stanford University 1979 to 1981 Specialities: Chemistry

Skills

Chemistry • Catalysis • Organic Chemistry • R&D • Organometallic Chemistry • Patents • Inorganic Chemistry • Commercialization • Due Diligence • Biofuels • Intellectual Property • Renewable Energy • Nanotechnology • Materials Science • Technology Transfer • Strategy • Patent Prosecution • Alternative Fuels • Inorganic Materials • Technical Writing • Research and Development • Intellectual Property Strategy • Patent Analysis • Process Chemistry • Biorenewables

Ranks

Certificate: Registered U.s. Patent Agent

Industries

Chemicals

Resumes

Resumes

Eric Evitt Photo 1

Patent Agent

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Location:
San Francisco, CA
Industry:
Chemicals
Work:
Wilson Sonsini Goodrich & Rosati
Patent Agent
Ere Consulting
President and Principal
Catalytica Jun 1996 - Mar 2002
Director, R and D
Catalytica Associates Jan 1982 - May 1996
Research Fellow; Senior Research Fellow; Program Group Director; Director Business Development
Education:
Stanford University 1979 - 1981
Caltech 1975 - 1980
Doctorates, Doctor of Philosophy, Chemistry University of Rochester 1971 - 1975
Bachelors, Bachelor of Science, Chemistry Palo Alto Senior High School
Skills:
Chemistry
Catalysis
Organic Chemistry
R&D
Organometallic Chemistry
Patents
Inorganic Chemistry
Commercialization
Due Diligence
Biofuels
Intellectual Property
Renewable Energy
Nanotechnology
Materials Science
Technology Transfer
Strategy
Patent Prosecution
Alternative Fuels
Inorganic Materials
Technical Writing
Research and Development
Intellectual Property Strategy
Patent Analysis
Process Chemistry
Biorenewables
Certifications:
Registered U.s. Patent Agent
United States Patent and Trademark Office, License 68609

Publications

Us Patents

Catalytic Process For Converting Lower Alkanes To Esters, Alcohols, And To Hydrocarbons

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US Patent:
53068556, Apr 26, 1994
Filed:
Nov 27, 1991
Appl. No.:
7/799446
Inventors:
Roy A. Periana - San Jose CA
Douglas J. Taube - Hayward CA
Henry Taube - Stanford CA
Eric R. Evitt - Mountain View CA
Assignee:
Catalytica, Inc. - Mountain View CA
International Classification:
C07C 200
US Classification:
585500
Abstract:
This invention is a process for converting lower alkanes into their corresponding esters and optionally into various intermediates (such as alcohols) and other liquid hydrocarbons. The alkanes are oxidatively converted to oxy-esters at high selectivity and conversion and at practical reaction rates using at least catalytic amounts of certain class "B" metals and/or metal ions defined by the Pearson definition as "soft" or "borderline". Desirable catalysts comprise such metals as Pd, Tl, Pt, Hg, and Au. If so desired, the alkyl oxy-esters may be converted to alcohols or other intermediates such as alkyl halides. The oxy-esters, alcohols, and other intermediates may optionally be converted to liquid hydrocarbons such as gasoline.

Process For Converting Lower Alkanes To Esters

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US Patent:
52331130, Aug 3, 1993
Filed:
Feb 15, 1991
Appl. No.:
7/656910
Inventors:
Roy A. Periana - San Jose CA
Eric R. Evitt - Mountain View CA
Henry Taube - Stanford CA
Assignee:
Catalytica, Inc. - Mountain View CA
International Classification:
C07C 200
US Classification:
585500
Abstract:
This invention is a process for converting lower alkanes into their corresponding esters and optionally into various intermediates (such as methanol) and other liquid hydrocarbons. The alkanes are oxidatively converted to oxy-esters at high selectivity using catalytic amounts of a Group VIII noble metal. If so desired, the alkyl oxy-esters may be converted to alcohols or other intermediates such as alkyl halides. The oxy-esters, alcohols, and other intermediates may optionally be converted to liquid hydrocarbons such as gasoline.

Palladium-Nitrile Ligand Catalyst System And Oxidation Process

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US Patent:
47389435, Apr 19, 1988
Filed:
Aug 21, 1987
Appl. No.:
7/089008
Inventors:
Janis Vasilevskis - Los Gatos CA
Paul L. Ridgway - Mountain View CA
Eric R. Evitt - Mountain View CA
Assignee:
Catalytica Associates - Mountain View CA
International Classification:
B01J 3128
B01J 3130
US Classification:
502165
Abstract:
A substantially chloride-free palladium oxidation system, comprising a palladium component, a copper component, and a ligand is described. The Wacker system, consisting of palladium and copper chlorides is also improved by the addition of a ligand. The palladium and copper counterion are independently selected from BF. sub. 4. sup. -, CF. sub. 3 COO. sup. -, SO. sub. 4. sup. =, and NO. sub. 3. sup. -. The ligand is preferably a nitrile-containing compound.

Palladium-Nitrile Ligand Catalyst System And Oxidation Processes

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US Patent:
48474215, Jul 11, 1989
Filed:
Jan 29, 1988
Appl. No.:
7/149839
Inventors:
Janis Vasilevskis - Los Gatos CA
Paul L. Ridgway - Mountain View CA
Eric R. Evitt - Mountain View CA
Assignee:
Catalytica, Associates - Mountain View CA
International Classification:
C07C 4534
US Classification:
568401
Abstract:
A substantially chloride-free palladium oxidation system, comprising a palladium component, a copper component, and a ligand is described. The Wacker system, consisting of palladium and copper chlorides is also improved by the addition of a ligand. The palladium and copper counterion are independently selected from BF. sub. 4. sup. --, CF. sub. 3 COO. sup. --, CH. sub. 3 COO. sup. --, SO. sub. 4. sup. dbd. , and NO. sub. 3. sup. --. The ligand is preferably a nitrile-containing compound.
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Eric R Evitt from Mountain View, CA, age ~71 Get Report