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In organic chemistry, organocatalysis is a form of catalysis in which the rate of a chemical reaction is increased by an organic catalyst. This "organocatalyst" consists of carbon , hydrogen , sulfur and other nonmetal elements found in organic compounds.
Organocatalysis is a subfield of catalysis that explores the potential of organic small molecules as catalysts, particularly for the enantioselective creation of chiral molecules. One strategy in this subfield is the use of chiral secondary amines to activate carbonyl compounds.
[13] [14] He is the editor-in-chief of the scientific journal Synlett. [15] As of 2021, he has an h-index of 95 according to Google Scholar [16] and of 86 according to Scopus. [17] Catalyst for asymmetric reactions, L-proline. List is considered to be one of the founders of organocatalysis, which uses non-metal and non-enzyme catalysts. [18]
Hydrogen-bond catalysis is a type of organocatalysis that relies on use of hydrogen bonding interactions to accelerate and control organic reactions. In biological systems, hydrogen bonding plays a key role in many enzymatic reactions, both in orienting the substrate molecules and lowering barriers to reaction. [1]
Proline organocatalysis is the use of proline as an organocatalyst in organic chemistry. This theme is often considered the starting point for the area of organocatalysis, even though early discoveries went unappreciated. [1] Modifications, such as MacMillan’s catalyst and Jorgensen's catalysts, proceed with excellent stereocontrol. [2]: 5574 [3]
Schreiner's thiourea, N,N'-bis3,5-bis(trifluormethyl)phenyl thiourea, combines all structural features for double H-bonding mediated organocatalysis: electron-poor; rigid structure; non-coordinating, electron withdrawing substituents in 3,4, and/or 5 position of a phenyl ring; the 3,5-bis(trifluoromethyl)phenyl-group is the preferred substituent
Unsaturated NHO. An N-heterocyclic olefin (NHO) is a neutral heterocyclic compound with a highly polarized, electron-rich C=C olefin attached to a heterocycle made up of two nitrogen atoms.
The Hajos–Parrish–Eder–Sauer–Wiechert and Barbas-List [1] reactions in organic chemistry are a family of proline-catalysed asymmetric aldol reactions.. In the 1970s, two research groups discovered (and published) almost simultaneously their discoveries of two related intramolecular reactions: Zoltan Hajos and David Parrish at Hoffmann-La Roche [2] [3] and Rudolf Wiechert et al at ...