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Mohammad N Namavari

from Palo Alto, CA
Age ~73

Mohammad Namavari Phones & Addresses

  • 756 Montrose Ave, Palo Alto, CA 94303
  • Menlo Park, CA
  • 832 Antoinette Ln, South San Francisco, CA 94080 (415) 983-1805 (650) 583-1805 (650) 983-1805
  • Forest Hills, NY
  • Los Angeles, CA
  • Santa Clara, CA

Work

Position: Craftsman/Blue Collar

Education

Degree: Associate degree or higher

Publications

Us Patents

Compounds And Methods Of Making Compounds

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US Patent:
20110059014, Mar 10, 2011
Filed:
Sep 3, 2010
Appl. No.:
12/875339
Inventors:
Mohammad Namavari - South San Francisco CA, US
Sanjiv Sam Gambhir - Portola Valley CA, US
Beverly S. Mitchell - Menlo Park CA, US
International Classification:
A61K 51/04
C07H 19/16
US Classification:
424 173, 536 2781
Abstract:
Embodiments of the present disclosure provide for compounds and methods of making compounds such as those shown in FIGS. A and B having formula 2, 3, 4, 5, 11, and 12 and formula 2′, 4′, and 11′, as well as uses for the compounds for imaging, and the like.

Synthesis Of N-Formyl-3,4-Di-T-Butoxycarbonyloxy-6-(Trimethylstannyl)-L-Phenylalanine Ethyl Ester And Its Regioselective Radiofluorodestannylation To 6- .Sup.18 F!Fluoro-1-Dopa

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US Patent:
55105220, Apr 23, 1996
Filed:
Feb 22, 1995
Appl. No.:
8/393428
Inventors:
Jorge R. Barrio - Agoura Hills CA
Allyson J. Bishop - Wahnemuhle, DE
Mohammad Namavari - Los Angeles CA
Gerald T. Bida - Shreveport LA
Assignee:
Regents of the University of California - Oakland CA
International Classification:
C07C22900
US Classification:
562446
Abstract:
A process for forming a 6-fluoro derivative of compounds in the L-Dopa family comprising the steps of protecting the groups attached to the benzene ring in the compound followed by serially reacting the protected compound with (a) iodine and silver trifluoroacetic acid; (b) Bb. sub. 3 ; (c) dit-butyldicarbonate; (d) hexamethyltin; (e) a fluoro compound; (f) hydrobromic acid; and (g) raising the pH to. ltoreq. 7.

Synthesis Of N-Formyl-3,4-Di-T-Butoxycarbonyloxy-6-(Trimethylstannyl)-L-Phenylalanine Ethyl Ester And Its Regioselective Radiofluorodestannylation To 6-[.Sup.18 F]Fluoro-L-Dopa

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US Patent:
53939085, Feb 28, 1995
Filed:
Jun 25, 1992
Appl. No.:
7/903915
Inventors:
Jorge R. Barrio - Agoura Hills CA
Allyson J. Bishop - Los Angeles CA
Mohammad Namavari - Los Angeles CA
International Classification:
C07F 722
C07C22900
US Classification:
556 87
Abstract:
A protected 6-trimethylstannyl dopa derivative has been synthesized for the as a precursor for the preparation of 6-[. sup. 18 F]fluoro-L-dopa. The tin derivative readily reacts with electrophilic radiofluorinating agents such as [. sup. 18 F]F. sub. 2, [. sup. 18 F]OF. sub. 2 and [. sup. 18 F]AcOF. The [. sup. 18 F]fluoro intermediate was easily hydrolyzed with HBr and the product 6-[. sup. 18 F]fluoro-L-dopa was isolated after HPLC purification in a maximum radiochemical yield of 23%, ready for human use.

Process For Producing 8-Fluoropurines

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US Patent:
58615032, Jan 19, 1999
Filed:
Apr 30, 1997
Appl. No.:
8/846424
Inventors:
Jorge R. Barrio - Agoura Hills CA
Mohammad Namavari - Los Angeles CA
Michael E. Phelps - Encino CA
Assignee:
The Regents of the University of California - Oakland CA
International Classification:
C07H 1916
C07D47300
US Classification:
536 2711
Abstract:
An efficient, regiocontrolled approach to the synthesis of 8-fluoropurines by direct fluorination of purines with dilute elemental fluorine, or acetyl hypofluorite, is provided. In a preferred embodiment, a purine compound is dissolved in a polar solvent and reacted with a dilute mixture of F. sub. 2 in He or other inert gas.

8-Fluoropurine Compounds

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US Patent:
62622544, Jul 17, 2001
Filed:
Nov 25, 1998
Appl. No.:
9/199975
Inventors:
Jorge R. Barrio - Agoura Hills CA
Mohammad Namavari - Los Angeles CA
Michael E. Phelps - Encino CA
Assignee:
The Regents of Univ. of California - Oakland CA
International Classification:
C07H 19167
C07H 19173
C07D47300
US Classification:
536 2711
Abstract:
An efficient, regiocontrolled approach to the synthesis of 8-fluoropurines by direct fluorination of purines with dilute elemental fluorine, or acetyl hypofluorite, is provided. In a preferred embodiment, a purine compound is dissolved in a polar solvent and reacted with a dilute mixture of F. sub. 2 in He or other inert gas.
Mohammad N Namavari from Palo Alto, CA, age ~73 Get Report