Organocapture - Revision history

Dragos: Fixed a formatting mistake.

2024-08-05T10:36:41Z

Fixed a formatting mistake.

← Older revision		Revision as of 12:36, 5 August 2024
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	=== Organocatalysis ===		=== Organocatalysis ===

			[1] B. List, R. A. Lerner, C. F. Barbas III. Proline-catalyzed direct asymmetric aldol reactions. ''J. Am. Chem. Soc.'' '''2000''', ''122'', 2395–2396. https://doi.org/10.1021/ja994280y

	~~[1] B. List, R. A. Lerner, C. F. Barbas III. Proline-catalyzed direct asymmetric aldol reactions. ''J. Am. Chem. Soc.'' '''2000''', ''122'', 2395–2396. https://doi.org/10.1021/ja994280y~~[2] D. W. C. MacMillan, The advent and development of organocatalysis. ''Nature'' '''2008''', ''455'', 304–308. https://doi.org/10.1038/nature07367		[2] D. W. C. MacMillan, The advent and development of organocatalysis. ''Nature'' '''2008''', ''455'', 304–308. https://doi.org/10.1038/nature07367

	=== Reference Organocapture ===		=== Reference Organocapture ===


	[3] P. Tremmel, H. Griesser, U. E. Steiner, C. Richert, How small heterocycles make a reaction network of amino acids and nucleotides efficient in water. ''Angew. Chem. Int. Ed.'' '''2019''', ''58'', 13087-13092. https://doi.org/10.1002/anie.201905427		[3] P. Tremmel, H. Griesser, U. E. Steiner, C. Richert, How small heterocycles make a reaction network of amino acids and nucleotides efficient in water. ''Angew. Chem. Int. Ed.'' '''2019''', ''58'', 13087-13092. https://doi.org/10.1002/anie.201905427

Dragos: Cleaned up the page formatting, redid the numbering of the references and added links to the cited papers.

2024-08-05T10:36:13Z

Cleaned up the page formatting, redid the numbering of the references and added links to the cited papers.

← Older revision		Revision as of 12:36, 5 August 2024
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			== Organocapture ==

	~~'''~~Organocapture~~'''~~


	When small organic molecules, rather than transition metal complexes, enzymes or mere acids/bases, catalyze a reaction, the term "organocatalysis" is used. Sometimes the "catalyst" increases the yield of a reaction without accelerating the reaction leading to the desired product by reducing the rate of competing reactions more than that of the desired reaction. When this happens and a covalent intermediate is involved, the term "organocapture" may be used.		When small organic molecules, rather than transition metal complexes, enzymes or mere acids/bases, catalyze a reaction, the term "organocatalysis" is used. Sometimes the "catalyst" increases the yield of a reaction without accelerating the reaction leading to the desired product by reducing the rate of competing reactions more than that of the desired reaction. When this happens and a covalent intermediate is involved, the term "organocapture" may be used.

			== References ==

			=== Organocatalysis ===
	~~'''References~~ Organocatalysis~~'''~~


	~~B. List, R. A. Lerner, C. F.Barbas III. Proline-catalyzed direct asymmetric aldol reactions. ''J. Am. Chem. Soc.'' '''2000''', ''122'', 2395–2396.~~


	~~D. W. C. MacMillan, The advent and development of organocatalysis. ''Nature'' '''2008''', ''455'', 304–308.~~


			[1] B. List, R. A. Lerner, C. F. Barbas III. Proline-catalyzed direct asymmetric aldol reactions. ''J. Am. Chem. Soc.'' '''2000''', ''122'', 2395–2396. https://doi.org/10.1021/ja994280y[2] D. W. C. MacMillan, The advent and development of organocatalysis. ''Nature'' '''2008''', ''455'', 304–308. https://doi.org/10.1038/nature07367

	~~'''~~Reference Organocapture~~'''~~		=== Reference Organocapture ===


	P. Tremmel, H. Griesser, U. E. Steiner, C. Richert, How small heterocycles make a reaction network of amino acids and nucleotides efficient in water. ''Angew. Chem. Int. Ed.'' '''2019''', ''58'', 13087-13092.		[3] P. Tremmel, H. Griesser, U. E. Steiner, C. Richert, How small heterocycles make a reaction network of amino acids and nucleotides efficient in water. ''Angew. Chem. Int. Ed.'' '''2019''', ''58'', 13087-13092. https://doi.org/10.1002/anie.201905427

Richert: Created page with " '''Organocapture''' When small organic molecules, rather than transition metal complexes, enzymes or mere acids/bases, catalyze a reaction, the term "organocatalysis" is used. Sometimes the "catalyst" increases the yield of a reaction without accelerating the reaction leading to the desired product by reducing the rate of competing reactions more than that of the desired reaction. When this happens and a covalent intermediate is involved, the term "organocapture" may..."

2024-07-31T09:33:03Z

Created page with " '''Organocapture''' When small organic molecules, rather than transition metal complexes, enzymes or mere acids/bases, catalyze a reaction, the term "organocatalysis" is used. Sometimes the "catalyst" increases the yield of a reaction without accelerating the reaction leading to the desired product by reducing the rate of competing reactions more than that of the desired reaction. When this happens and a covalent intermediate is involved, the term "organocapture" may..."

New page

'''Organocapture'''

When small organic molecules, rather than transition metal complexes, enzymes or mere acids/bases, catalyze a reaction, the term "organocatalysis" is used. Sometimes the "catalyst" increases the yield of a reaction without accelerating the reaction leading to the desired product by reducing the rate of competing reactions more than that of the desired reaction. When this happens and a covalent intermediate is involved, the term "organocapture" may be used.

'''References Organocatalysis'''

B. List, R. A. Lerner, C. F.Barbas III. Proline-catalyzed direct asymmetric aldol reactions. ''J. Am. Chem. Soc.'' '''2000''', ''122'', 2395–2396.

D. W. C. MacMillan, The advent and development of organocatalysis. ''Nature'' '''2008''', ''455'', 304–308.

'''Reference Organocapture'''

P. Tremmel, H. Griesser, U. E. Steiner, C. Richert, How small heterocycles make a reaction network of amino acids and nucleotides efficient in water. ''Angew. Chem. Int. Ed.'' '''2019''', ''58'', 13087-13092.