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Venkatram R Mereddy

age ~56

from Duluth, MN

Also known as:
  • Venkatram Reddy Mereddy
  • Venkatram Venkatram Mereddy
  • Venkatrdam R Mereddy
  • Venkatram Reddy
Phone and address:
1936 Chinook Dr, Duluth, MN 55811
2187282780

Venkatram Mereddy Phones & Addresses

  • 1936 Chinook Dr, Duluth, MN 55811 • 2187282780
  • Lafayette, IN
  • St Louis Pk, MN
  • W Lafayette, IN
  • 1869 Shoshone Dr APT 14, Lafayette, IN 47909

Work

  • Position:
    Food Preparation and Serving Related Occupations

Us Patents

  • Method Of Controlled Alcoholysis And Regeneration Of A Borohydride

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  • US Patent:
    7601797, Oct 13, 2009
  • Filed:
    May 10, 2005
  • Appl. No.:
    11/125796
  • Inventors:
    P. Veeraraghavan Ramachandran - West Lafayette IN, US
    Debasis Hazra - West Lafayette IN, US
    Venkatram Reddy Mereddy - Duluth MN, US
    Annyt Bhattacharyya - West Lafayette IN, US
  • Assignee:
    Purdue Research Foundation - West Lafayette IN
  • International Classification:
    C08G 78/08
    C01B 35/10
  • US Classification:
    528394, 423277
  • Abstract:
    Methods of controlled hydrolysis/alcoholysis and regeneration of a borohydride are disclosed. Examples of the present invention show that hydrolysis of sodium borohydride or lithium borohydride with dilute acid provides simultaneous generation of Hand boric acid for recycling. Other examples of the present invention show methods for regenerating a borohydride by reacting an aluminum hydride to a borate compound to provide a regenerated borohydride.
  • Stable Borane Reagents And Methods For Their Use

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  • US Patent:
    8263810, Sep 11, 2012
  • Filed:
    May 19, 2008
  • Appl. No.:
    12/123307
  • Inventors:
    Venkatram R. MeReddy - Duluth MN, US
    Kanth V. B. Josyula - Germantown WI, US
  • Assignee:
    Regents of the University of Minnesota - St. Paul MN
    Sigma-Aldrich Co. LLC - St. Louis MO
  • International Classification:
    C07F 5/02
  • US Classification:
    568 1
  • Abstract:
    The invention provides methods for storing boranes (e. g. B-allyldiisopinocampheylborane). The invention also provides stable compositions comprising boranes, as well as methods for carrying out allylboration at high temperature and/or in the presence of water.
  • Methods For Preparing Halohydrins And Methods For Preparing Epoxides

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  • US Patent:
    20070282137, Dec 6, 2007
  • Filed:
    Jun 1, 2007
  • Appl. No.:
    11/809821
  • Inventors:
    P. V. Ramachandran - West Lafayette IN, US
    Kamlesh J. Padiya - Maharashtra, IN
    Venkatram R. Mereddy - Duluth MN, US
  • International Classification:
    C07C 31/18
  • US Classification:
    568861
  • Abstract:
    The invention includes methods for preparing halohydrins and epoxides. A method of preparing halohydrins can include exposing (RCHXCHO—)SOto RCOOH to produce RCHXCHCOORand hydrolyzing the RCHXCHCOORto produce the halohydrin RCHXCHOH. Rand Rcan be the same or different single elements and/or organic groups and X can be a halogen. A method of preparing an epoxide can include combining a sulfuric acid containing solution with a halogen to produce a first mixture and exposing the first mixture to trifluoropropene to produce a second mixture. The second mixture can be combined with acetic acid to produce an acetyl halohydrin of trifluoropropene and the acetyl halohydrin can be hydrolyzed to form a halohydrin of trifluoropropene. The halohydrin can be converted to a trifluoropropyl epoxide.
  • Methods For Preparing Epoxides

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  • US Patent:
    20080114193, May 15, 2008
  • Filed:
    Nov 15, 2007
  • Appl. No.:
    11/985381
  • Inventors:
    P.V. Ramachandran - West Lafayette IN, US
    Kamlesh Padiya - Maharashtra, IN
    Venkatram Mereddy - Duluth MN, US
  • International Classification:
    C07C 31/34
  • US Classification:
    568841000
  • Abstract:
    The invention includes methods for preparing halohydrins and epoxides. A method of preparing halohydrins can include exposing (RCHXCHO—)SOto RCOOH to produce RCOOCHCHXRand hydrolyzing the RCOOCHCHXRto produce the halohydrin RCHXCHOH. Rand Rcan be the same or different single elements and/or organic groups and X can be a halogen. A method of preparing an epoxide can include combining a sulfuric acid containing solution with a halogen to produce a first mixture and exposing the first mixture to trifluoropropene to produce a second mixture. The second mixture can be combined with acetic acid to produce an acetyl halohydrin of trifluoropropene and the acetyl halohydrin can be hydrolyzed to form a halohydrin of trifluoropropene. The halohydrin can be converted to a trifluoropropyl epoxide.
  • Therapeutic Compound And Methods

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  • US Patent:
    20210114975, Apr 22, 2021
  • Filed:
    Oct 21, 2020
  • Appl. No.:
    17/076527
  • Inventors:
    - Minneapolis MN, US
    Venkatram R. Mereddy - Minneapolis MN, US
  • Assignee:
    Regents of the University of Minnesota - Minneapolis MN
  • International Classification:
    C07C 255/23
    A61P 35/00
  • Abstract:
    The invention provide a compound of formula I:or a salt thereof. The invention also provides pharmaceutical compositions comprising a compound of formula I or a pharmaceutically acceptable salt thereof, processes for preparing a compound of formula I or a pharmaceutically acceptable salt thereof, intermediates useful for preparing a compound of formula I or a pharmaceutically acceptable salt thereof, and therapeutic methods comprising the administration of a compound of formula I or a pharmaceutically acceptable salt thereof. The compounds and salts are useful for inhibiting glycolysis and mitochondrial function and are useful for treating cancer, autoimmune diseases, NASH, CGvHD, and obesity. The compounds and salts are are useful for treating transplant rejection.
  • Indole And Indazole Compounds And Therapeutic Uses Thereof

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  • US Patent:
    20190040016, Feb 7, 2019
  • Filed:
    Mar 20, 2017
  • Appl. No.:
    16/087069
  • Inventors:
    - Minneapolis MN, US
    Venkatram R. MEREDDY - Minneapolis MN, US
  • International Classification:
    C07D 231/56
    A61P 35/00
  • Abstract:
    Disclosed are Indole and Indazole derivatives, method for preparing these compounds, and methods for treating cancers.

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