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Reactions
3374 reactions imported from Wikipedia named-reactions and Organic Syntheses archives. Filter by source or search by name + summary.
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| Equation | Name | Summary | Source |
|---|---|---|---|
| HEXAHYDRO-1,3,5-TRIPROPIONYL-s-TRIAZINE (s-Triazine, hexahydro-1,3,5-tripropionyl) | Preparation of s-Triazine, hexahydro-1,3,5-tripropionyl. Submitted by W. O. Teeters and M. A. Gradsten1. DOI: 10.15227/orgsyn.030.0051. | Organic Syntheses | |
| HEXAHYDRO-2-(1H)-AZOCINONE (2(1H)-Azocinone, hexahydro-) | Preparation of 2(1H)-Azocinone, hexahydro-. Submitted by George A. Olah and Alexander P. Fung1. DOI: 10.15227/orgsyn.063.0188. | Organic Syntheses | |
| HEXAHYDROGALLIC ACID AND HEXAHYDROGALLIC ACID TRIACETATE (Cyclohexanecarboxylic acid, 3,4,5-triol and triacetate) | Preparation of Cyclohexanecarboxylic acid, 3,4,5-triol and triacetate. Submitted by Albert W. Burgstahler and Zoe J. Bithos1. DOI: 10.15227/orgsyn.042.0062. | Organic Syntheses | |
| HEXAHYDROXYBENZENE (Benzenehexol) | Preparation of Benzenehexol. Submitted by A. J. Fatiadi and W. F. Sager1. DOI: 10.15227/orgsyn.042.0066. | Organic Syntheses | |
| HEXAMETHYLBENZENE (Benzene, hexamethyl-) | Preparation of Benzene, hexamethyl-. Submitted by N. M. Cullinane, S. J. Chard, and C. W. C. Dawkins1. DOI: 10.15227/orgsyn.035.0073. | Organic Syntheses | |
| HEXAMETHYL DEWAR BENZENE (Bicyclo[2.2.0]hexa-2,5-diene, 1,2,3,4,5,6-hexamethyl-) | Preparation of Bicyclo[2.2.0]hexa-2,5-diene, 1,2,3,4,5,6-hexamethyl-. Submitted by Sami A. Shama and Carl C. Wamser1. DOI: 10.15227/orgsyn.061.0062. | Organic Syntheses | |
| HEXAMETHYLENE CHLOROHYDRIN (1-Hexanol, 6-chloro-) | Preparation of 1-Hexanol, 6-chloro-. Submitted by Kenneth N. Campbell and Armiger H. Sommers1. DOI: 10.15227/orgsyn.028.0065. | Organic Syntheses | |
| HEXAMETHYLENE DIISOCYANATE (Isocyanic acid, hexamethylene ester) | Preparation of Isocyanic acid, hexamethylene ester. Submitted by Mark W. Farlow1. DOI: 10.15227/orgsyn.031.0062. | Organic Syntheses | |
| HEXAMETHYLENE GLYCOL (1,6-Hexanediol) | Preparation of 1,6-Hexanediol. Submitted by W. A. Lazier, J. W. Hill, and W. J. Amend. DOI: 10.15227/orgsyn.019.0048. | Organic Syntheses | |
| HEXAMETHYLPHOSPHOROUS TRIAMIDE (Phosphorous triamide, hexamethyl-) | Preparation of Phosphorous triamide, hexamethyl-. Submitted by V. Mark1. DOI: 10.15227/orgsyn.046.0042. | Organic Syntheses | |
| HEXAPHENYLBENZENE (Benzene, hexaphenyl-) | Preparation of Benzene, hexaphenyl-. Submitted by Louis F. Fieser1. DOI: 10.15227/orgsyn.046.0044. | Organic Syntheses | |
| HIGHLY EFFICIENT ADDITION OF ACTIVATED METHYLENE COMPOUNDS TO ALKENES CATALYZED BY GOLD AND SILVER Addition | Preparation of HIGHLY EFFICIENT ADDITION OF ACTIVATED METHYLENE COMPOUNDS TO ALKENES CATALYZED BY GOLD AND SILVER. Submitted by Chao-Jun Li1 and Xiaoquan Yao. DOI: 10.15227/orgsyn.084.0222. | Organic Syntheses | |
| HIGHLY REACTIVE CALCIUM FOR THE PREPARATION OF ORGANOCALCIUM REAGENTS: 1-ADAMANTYL CALCIUM HALIDES AND THEIR ADDITION TO KETONES: 1-(1-ADAMANTYL)CYCLOHEXANOL (Cyclohexanol, 1-tricyclo[3.3.1.13,7]dec-1-yl) Addition | Preparation of Cyclohexanol, 1-tricyclo[3.3.1.13,7]dec-1-yl. Submitted by Reuben D. Rieke, Tse-Chong Wu, and Loretta I. Rieke1. DOI: 10.15227/orgsyn.072.0147. | Organic Syntheses | |
| HIGHLY REACTIVE MAGNESIUM FOR THE PREPARATION OF GRIGNARD REAGENTS: 1-NORBORNANECARBOXYLIC ACID (Bicyclo[2.2.1]heptane-1-carboxylic acid) Organometallic addition | Preparation of Bicyclo[2.2.1]heptane-1-carboxylic acid. Submitted by Reuben D. Rieke1, Stephen E. Bales, Phillip M. Hudnall, Timothy P. Burns, and Graham S. Poindexter. DOI: 10.15227/orgsyn.059.0085. | Organic Syntheses | |
| HIGH-YIELDING, LARGE-SCALE SYNTHESIS OF N-PROTECTED-β-AMINONITRILES: TERT-BUTYL (1R)-2-CYANO-1-PHENYLETHYLCARBAMATE | Preparation of HIGH-YIELDING, LARGE-SCALE SYNTHESIS OF N-PROTECTED-β-AMINONITRILES: TERT-BUTYL (1R)-2-CYANO-1-PHENYLETHYLCARBAMATE. Submitted by Fathia Mosa1, Carl Thirsk1, Michel Vaultier2, Graham Ma… | Organic Syntheses | |
| Hill reaction | The Hill reaction is the light-driven transfer of electrons from water to Hill reagents (non-physiological oxidants) in a direction against the chemical potential gradient as part of photosynthesis. R… | Wikipedia: Category:Name reactions | |
| Hinsberg oxindole synthesis | The Hinsberg oxindole synthesis is a method of preparing oxindoles from the bisulfite additions of glyoxal. It is named after its inventor Oscar Hinsberg. | Wikipedia: Category:Name reactions | |
| HIPPURIC ACID | Preparation of HIPPURIC ACID. Submitted by A. W. Ingersoll and S. H. Babcock. DOI: 10.15227/orgsyn.012.0040. | Organic Syntheses | |
| Hirao coupling Cross-coupling | In organic chemistry, Hirao coupling is a chemical reaction for the formation of carbon-phosphorus bonds using palladium cross-coupling. Hirao coupling expands the scope of carbon-phosphorus bond form… | Wikipedia: Category:Name reactions | |
| Hiyama coupling Cross-coupling | The Hiyama coupling is a palladium-catalyzed cross-coupling reaction of organosilanes with organic halides used in organic chemistry to form carbon–carbon bonds (C-C bonds). This reaction was discover… | Wikipedia: Category:Name reactions | |
| Hoesch reaction | The Hoesch reaction or Houben–Hoesch reaction is an organic reaction in which a nitrile reacts with an arene compound to form an aryl ketone. The reaction is a type of Friedel–Crafts acylation with hy… | Wikipedia: Category:Name reactions | |
| Hofmann elimination Rearrangement | Hofmann elimination is an elimination reaction of an amine to form alkenes. The least stable alkene (the one with the fewest substituents on the carbons of the double bond), called the Hofmann product… | Wikipedia: Category:Name reactions | |
| Hofmann–Löffler reaction Rearrangement | In organic chemistry, the Hofmann–Löffler reaction (also referred to as Hofmann–Löffler–Freytag reaction, Löffler–Freytag reaction, Löffler–Hofmann reaction, as well as Löffler's method) is a radical … | Wikipedia: Category:Name reactions | |
| Hofmann rearrangement Rearrangement | The Hofmann rearrangement (Hofmann degradation) is the organic reaction of a primary amide to a primary amine with one less carbon atom. The reaction involves oxidation of the nitrogen followed by rea… | Wikipedia: Category:Name reactions | |
| HOFMANN REARRANGEMENT UNDER MILDLY ACIDIC CONDITIONS USING [I,I-BIS(TRIFLUOROACETOXY)]IODOBENZENE: CYCLOBUTYLAMINE HYDROCHLORIDE FROM CYCLOBUTANECARBOXAMIDE (Cyclobutanamine hydrochloride) Rearrangement | Preparation of Cyclobutanamine hydrochloride. Submitted by Merrick R. Almond, Julie B. Stimmel, E. Alan Thompson, and G. Marc Loudon1. DOI: 10.15227/orgsyn.066.0132. | Organic Syntheses | |
| HOMOCONJUGATE ADDITION OF NUCLEOPHILES TO CYCLOPROPANE-1,1-DICARBOXYLATE DERIVATIVES: 2-OXO-1-PHENYL-3-PYRROLIDINECARBOXYLIC ACID (3-Pyrrolidinecarboxylic acid, 2-oxo-1-phenyl-) Addition | Preparation of 3-Pyrrolidinecarboxylic acid, 2-oxo-1-phenyl-. Submitted by Rajendra K. Singh and Samuel Danishefsky1. DOI: 10.15227/orgsyn.060.0066. | Organic Syntheses | |
| Homo-Favorskii rearrangement Rearrangement | The homo Favorskii rearrangement is the rearrangement of β-halo ketones and cyclobutanones, which in ring systems may yield ring contraction. This rearrangement takes place in the presence of a base, … | Wikipedia: Category:Name reactions | |
| HOMOGENEOUS CATALYTIC HYDROGENATION: DIHYDROCARVONE (2-Cyclohexen-1-one, 2-methyl-5-(1-methylethyl)-) Reduction | Preparation of 2-Cyclohexen-1-one, 2-methyl-5-(1-methylethyl)-. Submitted by Robert E. Ireland1 and P. Bey2. DOI: 10.15227/orgsyn.053.0063. | Organic Syntheses | |
| HOMOPHTHALIC ACID | Preparation of HOMOPHTHALIC ACID. Submitted by P. A. S. Smith and R. O. Kan1. DOI: 10.15227/orgsyn.044.0062. | Organic Syntheses | |
| HOMOPHTHALIC ACID AND ANHYDRIDE (Phenylacetic acid, o-carboxy-, and 1,3-Isochromandione) | Preparation of Phenylacetic acid, o-carboxy-, and 1,3-Isochromandione. Submitted by Oliver Grummitt, Richard Egan, and Allen Buck. DOI: 10.15227/orgsyn.029.0049. | Organic Syntheses | |
| HOMOVERATRIC ACID | Preparation of HOMOVERATRIC ACID. Submitted by H. R. Snyder, J. S. Buck, and W. S. Ide. DOI: 10.15227/orgsyn.015.0031. | Organic Syntheses | |
| Hooker reaction | In the Hooker reaction (1936) an alkyl chain in a certain naphthoquinone (phenomenon first observed in the compound lapachol) is reduced by one methylene unit as carbon dioxide in each potassium perma… | Wikipedia: Category:Name reactions | |
| Horner–Wadsworth–Emmons reaction | The Horner–Wadsworth–Emmons (HWE) reaction is a chemical reaction used in organic chemistry of stabilized phosphonate carbanions with aldehydes (or ketones) to produce predominantly E-alkenes. | Wikipedia: Category:Name reactions | |
| Hummers' method | Hummers' method is a chemical process that can be used to generate graphite oxide through the addition of potassium permanganate to a solution of graphite, sodium nitrate, and sulfuric acid. It is com… | Wikipedia: Category:Name reactions | |
| Hunsdiecker reaction | The Hunsdiecker reaction (also called the Borodin reaction or the Hunsdiecker–Borodin reaction) is a name reaction in organic chemistry whereby silver salts of carboxylic acids react with a halogen to… | Wikipedia: Category:Name reactions | |
| Hurd–Mori 1,2,3-thiadiazole synthesis | The Hurd–Mori 1,2,3-thiadiazole synthesis is a name reaction in organic chemistry that allows for the generation of 1,2,3-thiadiazoles through the reaction of hydrazone derivatives with an N-acyl or N… | Wikipedia: Category:Name reactions | |
| HYDRAZINE SULFATE | Preparation of HYDRAZINE SULFATE. Submitted by Roger Adams and B. K. Brown. DOI: 10.15227/orgsyn.002.0037. | Organic Syntheses | |
| HYDROCINNAMIC ACID | Preparation of HYDROCINNAMIC ACID. Submitted by A. W. Ingersoll. DOI: 10.15227/orgsyn.009.0042. | Organic Syntheses | |
| HYDROGENATION OF AROMATIC NUCLEI: 1-DECALOL Reduction | Preparation of HYDROGENATION OF AROMATIC NUCLEI: 1-DECALOL. Submitted by A. I. Meyers1, W. N. Beverung, and R. Gault2. DOI: 10.15227/orgsyn.051.0103. | Organic Syntheses | |
| HYDROGEN BROMIDE (ANHYDROUS) (Hydrobromic acid) | Preparation of Hydrobromic acid. Submitted by John R. Ruhoff, Robert E. Burnett, and E. Emmet Reid. DOI: 10.15227/orgsyn.015.0035. | Organic Syntheses | |
| HYDROGEN CYANIDE (ANHYDROUS) (Hydrocyanic acid) | Preparation of Hydrocyanic acid. Submitted by K. Ziegler. DOI: 10.15227/orgsyn.007.0050. | Organic Syntheses | |
| HYDROGENOLYSIS OF CARBON-HALOGEN BONDS WITH CHROMIUM(II)-EN PERCHLORATE: NAPHTHALENE FROM 1-BROMONAPHTHALENE | Preparation of HYDROGENOLYSIS OF CARBON-HALOGEN BONDS WITH CHROMIUM(II)-EN PERCHLORATE: NAPHTHALENE FROM 1-BROMONAPHTHALENE. Submitted by Ruth S. Wade and C. E. Castro1. DOI: 10.15227/orgsyn.052.0062. | Organic Syntheses | |
| HYDROMAGNESIATION REACTION OF PROPARGYLIC ALCOHOLS: (E)-3-PENTYL-2-NONENE-1,4-DIOL FROM 2-OCTYN-1-OL | Preparation of HYDROMAGNESIATION REACTION OF PROPARGYLIC ALCOHOLS: (E)-3-PENTYL-2-NONENE-1,4-DIOL FROM 2-OCTYN-1-OL. Submitted by Fumie Sato and Yuichi Kobayashi1. DOI: 10.15227/orgsyn.069.0106. | Organic Syntheses | |
| HYDROQUINONE DIACETATE (Hydroquinone, diacetate) | Preparation of Hydroquinone, diacetate. Submitted by W. W. Prichard. DOI: 10.15227/orgsyn.028.0068. | Organic Syntheses | |
| HYDROXYHYDROQUINONE TRIACETATE (1,2,4-Benzenetriol, triacetate) | Preparation of 1,2,4-Benzenetriol, triacetate. Submitted by E. B. Vliet. DOI: 10.15227/orgsyn.004.0035. | Organic Syntheses | |
| HYDROXYLAMINE HYDROCHLORIDE and ACETOXIME | Preparation of HYDROXYLAMINE HYDROCHLORIDE and ACETOXIME. Submitted by Waldo L. Semon. DOI: 10.15227/orgsyn.003.0061. | Organic Syntheses | |
| HYDROXYLATION OF ENOLATES WITH OXODIPEROXYMOLYBDENUM(PYRIDINE)(HEXAMETHYLPHOSPHORIC TRIAMIDE), MoO5·Py·HMPA(MoOPH): 3-HYDROXY-1,7,7-TRIMETHYLBICYCLO[2.2.1]HEPTAN-2-ONE (Bicyclo[2.2.1]heptan-2-one, 3-hydroxy-1,7,7-trimethyl-) | Preparation of Bicyclo[2.2.1]heptan-2-one, 3-hydroxy-1,7,7-trimethyl-. Submitted by Edwin Vedejs and S. Larsen1. DOI: 10.15227/orgsyn.064.0127. | Organic Syntheses | |
| HYDROXYMETHYLFERROCENE (Iron, cyclopentadienyl[(hydroxymethyl)cyclopentadienyl]-) | Preparation of Iron, cyclopentadienyl[(hydroxymethyl)cyclopentadienyl]-. Submitted by Daniel Lednicer, T. Arthur Mashburn, Jr., and Charles R. Hauser1. DOI: 10.15227/orgsyn.040.0052. | Organic Syntheses | |
| HYDROXYUREA (Urea, hydroxy-) | Preparation of Urea, hydroxy-. Submitted by R. Deghenghi1. DOI: 10.15227/orgsyn.040.0060. | Organic Syntheses | |
| IMIDAZOLE | Preparation of IMIDAZOLE. Submitted by H. R. Snyder, R. G. Handrick, and L. A. Brooks. DOI: 10.15227/orgsyn.022.0065. | Organic Syntheses |
