Process for chemical reaction of amino acids and amides yielding selective conversion products
Abstract
The invention relates to processes for converting amino acids and amides to desirable conversion products including pyrrolidines, pyrrolidinones, and other N-substituted products. L-glutamic acid and L-pyroglutamic acid provide general reaction pathways to numerous and valuable selective conversion products with varied potential industrial uses.
- Inventors:
-
- Kennewick, WA
- Issue Date:
- Research Org.:
- Pacific Northwest National Laboratory (PNNL), Richland, WA (United States)
- Sponsoring Org.:
- USDOE
- OSTI Identifier:
- 908427
- Patent Number(s):
- 7049446
- Application Number:
- 10/841,687
- Assignee:
- Battelle Memorial Institute (Richland, WA)
- Patent Classifications (CPCs):
-
C - CHEMISTRY C07 - ORGANIC CHEMISTRY C07D - HETEROCYCLIC COMPOUNDS
- DOE Contract Number:
- AC06-76RL01830
- Resource Type:
- Patent
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
Citation Formats
Holladay, Jonathan E. Process for chemical reaction of amino acids and amides yielding selective conversion products. United States: N. p., 2006.
Web.
Holladay, Jonathan E. Process for chemical reaction of amino acids and amides yielding selective conversion products. United States.
Holladay, Jonathan E. Tue .
"Process for chemical reaction of amino acids and amides yielding selective conversion products". United States. https://www.osti.gov/servlets/purl/908427.
@article{osti_908427,
title = {Process for chemical reaction of amino acids and amides yielding selective conversion products},
author = {Holladay, Jonathan E},
abstractNote = {The invention relates to processes for converting amino acids and amides to desirable conversion products including pyrrolidines, pyrrolidinones, and other N-substituted products. L-glutamic acid and L-pyroglutamic acid provide general reaction pathways to numerous and valuable selective conversion products with varied potential industrial uses.},
doi = {},
journal = {},
number = ,
volume = ,
place = {United States},
year = {2006},
month = {5}
}
Works referenced in this record:
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journal, February 1938
- Sauer, John C.; Adkins, Homer
- Journal of the American Chemical Society, Vol. 60, Issue 2
Stereoretentive C−H Bond Activation in the Aqueous Phase Catalytic Hydrogenation of Amino Acids to Amino Alcohols
journal, February 2003
- Jere, Frank T.; Miller, Dennis J.; Jackson, James E.
- Organic Letters, Vol. 5, Issue 4
Hydrogenation of Optically Active Compounds over Nickel and Copper—Chromium Oxide
journal, March 1934
- Bowden, Everett; Adkins, Homer
- Journal of the American Chemical Society, Vol. 56, Issue 3
Ruthenium-catalyzed Hydrogenation of Acids to Alcohols
journal, July 1955
- Carnahan, J. E.; Ford, T. A.; Gresham, W. F.
- Journal of the American Chemical Society, Vol. 77, Issue 14
Rhenium and Its Compounds as Hydrogenation Catalysts. III. Rhenium Heptoxide 1,2,3
journal, December 1959
- Broadbent, H. Smith; Campbell, Graham C.; Bartley, William J.
- The Journal of Organic Chemistry, Vol. 24, Issue 12