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  2. Michael addition reaction - Wikipedia

    en.wikipedia.org/wiki/Michael_Addition_Reaction

    Others, however, insist that such a usage is an abuse of terminology, and limit the Michael addition to the formation of carbon–carbon bonds through the addition of carbon nucleophiles. The terms oxa-Michael reaction and aza-Michael reaction [2] have been used to refer to the 1,4-addition of oxygen and nitrogen nucleophiles, respectively. The ...

  3. Polyaspartic esters - Wikipedia

    en.wikipedia.org/wiki/Polyaspartic_esters

    To manufacture a polyaspartic ester, an amine is reacted with dialkyl maleate by the aza-Michael reaction. [8]Diethyl maleate is the usual maleate used. This converts the primary amines to secondary amines and also introduces bulky groups to the molecule which causes steric hindrance, slowing the reaction down.

  4. Knorr pyrrole synthesis - Wikipedia

    en.wikipedia.org/wiki/Knorr_pyrrole_synthesis

    The Knorr pyrrole synthesis is a widely used chemical reaction that synthesizes substituted pyrroles (3). [1] [2] [3] The method involves the reaction of an α-amino-ketone (1) and a compound containing an electron-withdrawing group (e.g. an ester as shown) α to a carbonyl group (2). [4] The Knorr pyrrole synthesis

  5. Lewis acid catalysis - Wikipedia

    en.wikipedia.org/wiki/Lewis_Acid_Catalysis

    Two common modes of Lewis acid catalysis in reactions with polar mechanisms. In reactions with polar mechanisms, Lewis acid catalysis often involves binding of the catalyst to Lewis basic heteroatoms and withdrawing electron density, which in turn facilitates heterolytic bond cleavage (in the case of Friedel-Crafts reaction) or directly activates the substrate toward nucleophilic attack (in ...

  6. Thiourea organocatalysis - Wikipedia

    en.wikipedia.org/wiki/Thiourea_organocatalysis

    Unlike classical catalysts, these organocatalysts interact by non-covalent interactions, especially hydrogen bonding ("partial protonation"). The scope of these small-molecule H-bond donors termed (thio)urea organocatalysis covers both non-stereoselective and stereoselective reactions.

  7. Henry reaction - Wikipedia

    en.wikipedia.org/wiki/Henry_reaction

    The aza-Henry reaction is also used to produce nitroamines and can be a reliable synthetic route for the synthesis of vicinal diamines. [13] Perhaps one of the most synthetically useful modifications to the Henry reaction is the use of an organocatalyst. [2] [12] [14] The catalytic cycle is shown below. Henry reaction synthetic scheme

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  9. Hydrogen-bond catalysis - Wikipedia

    en.wikipedia.org/wiki/Hydrogen-bond_catalysis

    Using a chiral BINOL catalyst, for instance, the Morita-Baylis-Hillman reaction involving the addition of enones to aldehydes can be effected with high enantioselectivity. [5] The nucleophile is an enolate-type species generated from the conjugate addition of PEt 3 to the enone, and adds enantioselectively to the aldehyde coordinated to catalyst.

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