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- {{r|Amine gas treating}}247 bytes (29 words) - 09:39, 6 March 2024
- {{r|Amine}}171 bytes (19 words) - 10:33, 3 October 2009
- ...o activate [[carboxylic acid]]s for coupling with either [[alcohol]]s or [[amine]]s to form [[ester]] or [[amide]] products. It is similar to [[N,N'-dicycl453 bytes (63 words) - 11:31, 3 October 2009
- {{r|Amine gas treating}}290 bytes (33 words) - 09:52, 6 March 2024
- {{r|amine}}178 bytes (23 words) - 16:09, 4 November 2010
- {{r|Amine gas treating}}295 bytes (35 words) - 09:39, 6 March 2024
- {{r|Amine gas treating}}295 bytes (35 words) - 09:39, 6 March 2024
- {{r|Amine gas treating}}473 bytes (56 words) - 17:48, 16 June 2010
- ...ylic acid]]s for subsequent coupling with either [[alcohol]]s or primary [[amine]]s to form [[ester]]s or [[amide]]s. It is a [[carbodiimide]] type of reag480 bytes (68 words) - 10:12, 13 March 2024
- {{r|Amine gas treating}}354 bytes (43 words) - 09:39, 6 March 2024
- {{r|Amine gas treating}}462 bytes (56 words) - 12:12, 18 March 2012
- {{r|Amine gas treating}}456 bytes (53 words) - 09:39, 6 March 2024
- {{r|Amine gas treating}}449 bytes (56 words) - 03:48, 1 March 2011
- {{r|Amine gas treating}}379 bytes (49 words) - 09:27, 6 March 2024
- {{r|Amine gas treating}}555 bytes (69 words) - 09:39, 6 March 2024
- {{r|Amine}}319 bytes (34 words) - 10:40, 3 October 2009
- ...ed to activate [[carboxylic acid]]s for subsequent coupling with primary [[amine]]s, producing an [[amide]] compound. The carboxyl group is often converted ....png|left|350px|'''Scheme 2''':Coupling of a carboxylic acid and a primary amine via O-acylisourea ester and NHS ester intermediates.}}3 KB (480 words) - 12:22, 27 August 2010
- {{r|Amine gas treating}}532 bytes (68 words) - 09:39, 6 March 2024
- ...queous solutions of various [[alkanol]]s (commonly referred to as simply [[amine]]s) to remove [[hydrogen sulphide]] (H<sub>2</sub>S) and [[carbon dioxide]] ==Description of a typical amine treater==9 KB (1,476 words) - 09:37, 6 March 2024
- ...queous solutions of various [[alkanol]]s (commonly referred to as simply [[amine]]s) to remove [[hydrogen sulphide]] (H<sub>2</sub>S) and [[carbon dioxide]] ==Description of a typical amine treater==9 KB (1,470 words) - 09:37, 6 March 2024
- {{r|Biogenic amine receptor}}491 bytes (62 words) - 10:50, 11 January 2010
- *HN3: Tris(2-chloroethyl)amine (555-77-1)647 bytes (77 words) - 17:05, 22 June 2009
- {{r|Amine}}575 bytes (73 words) - 10:33, 23 March 2024
- {{r|Biogenic amine receptor}}549 bytes (69 words) - 16:47, 11 January 2010
- {{r|Amine}}581 bytes (75 words) - 19:42, 11 January 2010
- {{r|Biogenic amine receptor}}615 bytes (78 words) - 14:03, 1 April 2024
- {{r|Amine}}597 bytes (78 words) - 18:28, 11 January 2010
- {{r|Amine}}549 bytes (72 words) - 19:15, 11 January 2010
- {{r|Biogenic amine receptor}}608 bytes (77 words) - 19:26, 11 January 2010
- {{r|Biogenic amine receptor}}586 bytes (73 words) - 20:18, 11 January 2010
- {{r|Biogenic amine receptor}}639 bytes (81 words) - 19:45, 11 January 2010
- ...mistry]], '''methylenetetrahydrofolate reductase''' is a "[[flavoprotein]] amine oxidoreductase that catalyzes the reversible conversion of [[5-methyltetrah846 bytes (93 words) - 23:50, 16 November 2008
- ===Tertiary amine tricyclics=== ...include [[amitriptyline]], [[doxepin]], and [[imipramine]] have a tertiary-amine side chain block both [[serotonin]] and [[norepinephrine]] and increase [[p5 KB (622 words) - 14:32, 2 February 2023
- {{r|Biogenic amine receptor}}657 bytes (82 words) - 18:58, 11 January 2010
- {{r|Amine}}850 bytes (113 words) - 04:59, 4 August 2009
- {{r|Amine}}602 bytes (81 words) - 19:38, 11 January 2010
- {{r|Amine gas treating}}837 bytes (108 words) - 09:39, 6 March 2024
- ...s''' are "a group of membrane transport proteins that transport [[biogenic amine]] derivatives of catechol across the plasma membrane. Catecholamine plasma706 bytes (82 words) - 05:29, 30 September 2009
- {{r|Biogenic amine receptor}}885 bytes (112 words) - 17:13, 11 January 2010
- {{r|Biogenic amine receptor}}918 bytes (116 words) - 14:21, 8 March 2024
- {{r|Amine gas treating}} {{r|Amine}}3 KB (351 words) - 21:51, 16 August 2010
- In [[pharmacology]], '''tiotropium''' is a derivative of the quaternary amine [[scopolamine]] and is classified as a [[parasympatholytic]], [[cholinergic878 bytes (104 words) - 14:51, 23 June 2011
- {{r|amine}}738 bytes (114 words) - 20:53, 18 March 2011
- {{r|Amine gas treating}}809 bytes (98 words) - 00:31, 31 January 2010
- *Nitriles are reduced to [[amine|amines]] by [[hydrogen]] and a [[nickel]] catalyst827 bytes (113 words) - 17:46, 28 October 2010
- {{r|Biogenic amine receptor}}1,006 bytes (130 words) - 10:50, 11 January 2010
- ...those impurities to acceptable levels, commonly by an [[Amine gas treating|amine gas treater]] or similar process.<ref name=NatGasOrg/><ref>[http://www.eia.3 KB (430 words) - 09:44, 6 March 2024
- {{r|Biogenic amine receptor}}1 KB (148 words) - 16:03, 11 January 2010
- {{r|Biogenic amine receptor}}1 KB (148 words) - 16:21, 11 January 2010
- ...st, a copper(I) cocatalyst, and an excess of a secondary or tertiary alkyl amine. This reaction has proven to be extremely valuable for many multi-component1 KB (156 words) - 18:22, 20 December 2007