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- Nitroaldol_reaction abstract "The Henry Reaction (also referred to as the nitro-aldol reaction) is a classic carbon–carbon bond formation reaction in organic chemistry. Discovered in 1895 by L. Henry, it is the combination of a nitroalkane and an aldehyde or ketone in the presence of a base to form β-Nitro alcohols. This type of reaction is commonly referred to as a "nitro-aldol" reaction (nitroalkane, aldehyde, and alcohol) It is nearly analogous to the aldol reaction that had been discovered 23 years prior that couples two carbonyl compounds to form β-hydroxy carbonyl compounds known as "aldols" (aldehyde and alcohol). The Henry reaction is a useful technique in the area organic chemistry due to the synthetic utility of its corresponding products, as they can be easily converted to other useful synthetic intermediates. These conversions include subsequent dehydration to yield nitroalkenes, oxidation of the secondary alcohol to yield α-nitro ketones, or reduction of the nitro group to yield β-amino alcohols.Many of these uses have been exemplified in the syntheses of various pharmaceuticals including the β-blocker (S)-propranolol, the HIV protease inhibitor Amprenavir (Vertex 478), and construction of the carbohydrate subunit of the anthracycline class of antibiotics, L-Acosamine. The synthetic scheme of the L-Acosamine synthesis can be found in the Examples section of this article.".
- Nitroaldol_reaction thumbnail HenryScheme1.png?width=300.
- Nitroaldol_reaction wikiPageExternalLink Henry_startAnimGif.gif.
- Nitroaldol_reaction wikiPageID "2038911".
- Nitroaldol_reaction wikiPageLength "14071".
- Nitroaldol_reaction wikiPageOutDegree "43".
- Nitroaldol_reaction wikiPageRevisionID "667316333".
- Nitroaldol_reaction wikiPageWikiLink (S)-hydroxynitrile_lyase.
- Nitroaldol_reaction wikiPageWikiLink Acosamine.
- Nitroaldol_reaction wikiPageWikiLink Aldehyde.
- Nitroaldol_reaction wikiPageWikiLink Aldol_reaction.
- Nitroaldol_reaction wikiPageWikiLink Amprenavir.
- Nitroaldol_reaction wikiPageWikiLink Arabidopsis_thaliana.
- Nitroaldol_reaction wikiPageWikiLink Asymmetric_synthesis.
- Nitroaldol_reaction wikiPageWikiLink Cannizaro_reaction.
- Nitroaldol_reaction wikiPageWikiLink Cannizzaro_reaction.
- Nitroaldol_reaction wikiPageWikiLink Catalysis.
- Nitroaldol_reaction wikiPageWikiLink Catalyst.
- Nitroaldol_reaction wikiPageWikiLink Category:Carbon-carbon_bond_forming_reactions.
- Nitroaldol_reaction wikiPageWikiLink Chiral_ligand.
- Nitroaldol_reaction wikiPageWikiLink Diastereomer.
- Nitroaldol_reaction wikiPageWikiLink Diastereomers.
- Nitroaldol_reaction wikiPageWikiLink Diastereoselective.
- Nitroaldol_reaction wikiPageWikiLink Diisopropylethylamine.
- Nitroaldol_reaction wikiPageWikiLink Dipole.
- Nitroaldol_reaction wikiPageWikiLink Enantiomer.
- Nitroaldol_reaction wikiPageWikiLink Enantiomers.
- Nitroaldol_reaction wikiPageWikiLink Enantioselective.
- Nitroaldol_reaction wikiPageWikiLink Enantioselective_synthesis.
- Nitroaldol_reaction wikiPageWikiLink Ephedrine.
- Nitroaldol_reaction wikiPageWikiLink Hevea_brasiliensis.
- Nitroaldol_reaction wikiPageWikiLink Ketone.
- Nitroaldol_reaction wikiPageWikiLink N,N-Diisopropylethylamine.
- Nitroaldol_reaction wikiPageWikiLink Nitro_compound.
- Nitroaldol_reaction wikiPageWikiLink Nitroalkane.
- Nitroaldol_reaction wikiPageWikiLink Nitroalkene.
- Nitroaldol_reaction wikiPageWikiLink Nitromethane.
- Nitroaldol_reaction wikiPageWikiLink Organic_chemistry.
- Nitroaldol_reaction wikiPageWikiLink Organocatalysis.
- Nitroaldol_reaction wikiPageWikiLink Organocatalyst.
- Nitroaldol_reaction wikiPageWikiLink Propranolol.
- Nitroaldol_reaction wikiPageWikiLink Quinine.
- Nitroaldol_reaction wikiPageWikiLink Stereoselectivity.
- Nitroaldol_reaction wikiPageWikiLink Steric_effects.
- Nitroaldol_reaction wikiPageWikiLink Triflate_salt.
- Nitroaldol_reaction wikiPageWikiLink Trifluoromethanesulfonate.
- Nitroaldol_reaction wikiPageWikiLink Zinc.
- Nitroaldol_reaction wikiPageWikiLink File:Best1.png.
- Nitroaldol_reaction wikiPageWikiLink File:Canz.png.
- Nitroaldol_reaction wikiPageWikiLink File:Chinchura.png.
- Nitroaldol_reaction wikiPageWikiLink File:HenryRReactionApplication.png.
- Nitroaldol_reaction wikiPageWikiLink File:HenryScheme1.png.
- Nitroaldol_reaction wikiPageWikiLink File:Henry_Reaction_Mechanism_V.1.png.
- Nitroaldol_reaction wikiPageWikiLink File:Newman5.png.
- Nitroaldol_reaction wikiPageWikiLink File:OrganocatalysisScheme.png.
- Nitroaldol_reaction wikiPageWikiLink File:Selectivity3.png.
- Nitroaldol_reaction wikiPageWikiLink File:Synthesis_of_L-acosamine.svg.
- Nitroaldol_reaction wikiPageWikiLinkText "Nitroaldol reaction".
- Nitroaldol_reaction wikiPageWikiLinkText "nitroaldol reaction".
- Nitroaldol_reaction wikiPageWikiLinkText "nitroaldol".
- Nitroaldol_reaction hasPhotoCollection Nitroaldol_reaction.
- Nitroaldol_reaction wikiPageUsesTemplate Template:Reflist.
- Nitroaldol_reaction subject Category:Carbon-carbon_bond_forming_reactions.
- Nitroaldol_reaction hypernym Reaction.
- Nitroaldol_reaction type Disease.
- Nitroaldol_reaction type Reaction.
- Nitroaldol_reaction comment "The Henry Reaction (also referred to as the nitro-aldol reaction) is a classic carbon–carbon bond formation reaction in organic chemistry. Discovered in 1895 by L. Henry, it is the combination of a nitroalkane and an aldehyde or ketone in the presence of a base to form β-Nitro alcohols.".
- Nitroaldol_reaction label "Nitroaldol reaction".
- Nitroaldol_reaction sameAs Henry-Reaktion.
- Nitroaldol_reaction sameAs Reacción_de_Henry.
- Nitroaldol_reaction sameAs Réaction_de_Henry.
- Nitroaldol_reaction sameAs ヘンリー反応.
- Nitroaldol_reaction sameAs Henry-reactie.
- Nitroaldol_reaction sameAs Reação_de_Henry.
- Nitroaldol_reaction sameAs m.06gxbf.
- Nitroaldol_reaction sameAs Реакция_Анри.
- Nitroaldol_reaction sameAs Q903747.
- Nitroaldol_reaction sameAs Q903747.
- Nitroaldol_reaction wasDerivedFrom Nitroaldol_reaction?oldid=667316333.
- Nitroaldol_reaction depiction HenryScheme1.png.
- Nitroaldol_reaction isPrimaryTopicOf Nitroaldol_reaction.