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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 |
|---|---|---|---|
| BARBITURIC ACID | Preparation of BARBITURIC ACID. Submitted by J. B. Dickey and A. R. Gray. DOI: 10.15227/orgsyn.018.0008. | Organic Syntheses | |
| Bargellini reaction | The Bargellini reaction is a chemical reaction discovered in 1906 by Italian chemist Guido Bargellini. The original reaction was a mixture of the reagents phenol, chloroform, and acetone in the presen… | Wikipedia: Category:Name reactions | |
| Bartoli indole synthesis | The Bartoli indole synthesis (also called the Bartoli reaction) is the chemical reaction of ortho-substituted nitroarenes and nitrosoarenes with vinyl Grignard reagents to form substituted indoles. | Wikipedia: Category:Name reactions | |
| Barton decarboxylation | The Barton decarboxylation is a radical reaction in which a carboxylic acid is converted to a thiohydroxamate ester (commonly referred to as a Barton ester). The product is then heated in the presenc… | Wikipedia: Category:Name reactions | |
| Barton–Kellogg reaction | The Barton–Kellogg reaction is a coupling reaction between a diazo compound and a thioketone, giving an alkene by way of an episulfide intermediate.[1][2][3] The Barton–Kellogg reaction is also known… | Wikipedia: Category:Name reactions | |
| Barton–McCombie deoxygenation | The Barton–McCombie deoxygenation is an organic reaction in which a hydroxy functional group in an organic compound is replaced by a hydrogen to give an alkyl group. It is named after British chemists… | Wikipedia: Category:Name reactions | |
| Barton nitrite ester reaction | The Barton reaction, also known as the Barton nitrite ester reaction, is a photochemical reaction that involves the photolysis of an alkyl nitrite to form a δ-nitroso alcohol. | Wikipedia: Category:Name reactions | |
| Barton–Zard reaction | The Barton–Zard reaction is a route to pyrrole derivatives via the reaction of a nitroalkene with an α-isocyanide under basic conditions. It is named after Derek Barton and Samir Zard who first report… | Wikipedia: Category:Name reactions | |
| BASE-INDUCED REARRANGEMENT OF EPOXIDES TO ALLYLIC ALCOHOLS: trans-PINOCARVEOL (Bicyclo[3.3.1]heptan-3-ol, 6,6-dimethyl-2-methylene-, (1α,3α,5α-) Rearrangement | Preparation of Bicyclo[3.3.1]heptan-3-ol, 6,6-dimethyl-2-methylene-, (1α,3α,5α-. Submitted by J. K. Crandall1 and L. C. Crawley. DOI: 10.15227/orgsyn.053.0017. | Organic Syntheses | |
| Baudisch reaction | In organic chemistry, the Baudisch reaction is a process for the synthesis of nitrosophenols using metal ions. Although the products are of limited value, the reaction is of historical interest as an … | Wikipedia: Category:Name reactions | |
| Baylis–Hillman reaction | In organic chemistry, the Baylis–Hillman, Morita–Baylis–Hillman, or MBH reaction is a carbon–carbon bond-forming reaction between an activated alkene and a carbon electrophile in the presence of a nuc… | Wikipedia: Category:Name reactions | |
| Bechamp reaction | In organic synthesis the Béchamp reaction is used for producing arsonic acids from activated aromatic substrates. The reaction is an electrophilic aromatic substitution, using arsenic acid as the elec… | Wikipedia: Category:Name reactions | |
| Béchamp reduction Reduction | The Béchamp reduction (or Béchamp process) is a chemical reaction that converts aromatic nitro compounds to their corresponding anilines using iron as the reductant: | Wikipedia: Category:Name reactions | |
| Beckmann rearrangement Rearrangement | The Beckmann rearrangement, named after the German chemist Ernst Otto Beckmann (1853–1923), is a rearrangement of an oxime functional group to an amide functional group. The rearrangement has also bee… | Wikipedia: Category:Name reactions | |
| Belousov–Zhabotinsky reaction | A Belousov–Zhabotinsky reaction, or BZ reaction, is one of a class of reactions that serve as a classical example of non-equilibrium thermodynamics, resulting in the establishment of a nonlinear chemi… | Wikipedia: Category:Name reactions | |
| Benary reaction | The Benary reaction is an organic reaction. In 1931 Erich Bénary discovered that β-(N,N-dialkylamino)-vinyl ketones reacted with Grignard reagents in a 1,4-addition to give α,β-unsaturated ketones, α,… | Wikipedia: Category:Name reactions | |
| BENZALACETONE (3-Buten-2-one, 4-phenyl-) | Preparation of 3-Buten-2-one, 4-phenyl-. Submitted by N. L. Drake and P. Allen, Jr. DOI: 10.15227/orgsyn.003.0017. | Organic Syntheses | |
| BENZALACETONE DIBROMIDE (2-Butanone, 3,4-dibromo-4-phenyl-) | Preparation of 2-Butanone, 3,4-dibromo-4-phenyl-. Submitted by Norman H. Cromwell and Richard Benson. DOI: 10.15227/orgsyn.027.0005. | Organic Syntheses | |
| BENZALACETOPHENONE (Chalcone) | Preparation of Chalcone. Submitted by E. P. Kohler and H. M. Chadwell. DOI: 10.15227/orgsyn.002.0001. | Organic Syntheses | |
| BENZALANILINE (Aniline, N-benzylidene-) | Preparation of Aniline, N-benzylidene-. Submitted by Lucius A. Bigelow and Harry Eatough. DOI: 10.15227/orgsyn.008.0022. | Organic Syntheses | |
| BENZALPHTHALIDE (Phthalide, 3-benzylidene-) | Preparation of Phthalide, 3-benzylidene-. Submitted by Richard Weiss. DOI: 10.15227/orgsyn.013.0010. | Organic Syntheses | |
| BENZALPINACOLONE (1-Penten-3-one, 4,4-dimethyl-1-phenyl-) Rearrangement | Preparation of 1-Penten-3-one, 4,4-dimethyl-1-phenyl-. Submitted by G. A. Hill and G. M. Bramann. DOI: 10.15227/orgsyn.005.0015. | Organic Syntheses | |
| BENZANILIDE | Preparation of BENZANILIDE. Submitted by Carl N. Webb. DOI: 10.15227/orgsyn.007.0006. | Organic Syntheses | |
| BENZANTHRONE (7-Benz[de]anthracene-7-one) | Preparation of 7-Benz[de]anthracene-7-one. Submitted by L. C. Macleod and C. F. H. Allen. DOI: 10.15227/orgsyn.014.0004. | Organic Syntheses | |
| BENZENEBORONIC ANHYDRIDE (Boroxin, triphenyl-) | Preparation of Boroxin, triphenyl-. Submitted by Robert M. Washburn, Ernest Levens, Charles F. Albright, and Franklin A. Billig1. DOI: 10.15227/orgsyn.039.0003. | Organic Syntheses | |
| BENZENEDIAZONIUM-2-CARBOXYLATE AND BIPHENYLENE (Benzenediazonium, o-carboxy-, hydroxide, inner salt) | Preparation of Benzenediazonium, o-carboxy-, hydroxide, inner salt. Submitted by Francis M. Logullo, Arnold H. Seitz, and Lester Friedman1. DOI: 10.15227/orgsyn.048.0012. | Organic Syntheses | |
| BENZENESULFONYL CHLORIDE ((A) and (B) (from Sodium Benzenesulfonate)) | Preparation of (A) and (B) (from Sodium Benzenesulfonate). Submitted by Roger Adams and C. S. Marvel. DOI: 10.15227/orgsyn.001.0021. | Organic Syntheses | |
| BENZHYDRYL β-CHLOROETHYL ETHER (Ether, benzohydryl 2-chloroethyl) | Preparation of Ether, benzohydryl 2-chloroethyl. Submitted by Shigehiko Sugasawa and Kunio Fujiwara1. DOI: 10.15227/orgsyn.033.0011. | Organic Syntheses | |
| BENZIL | Preparation of BENZIL. Submitted by H. T. Clarke and E. E. Dreger. DOI: 10.15227/orgsyn.006.0006. | Organic Syntheses | |
| BENZILIC ACID | Preparation of BENZILIC ACID. Submitted by Donald A. Ballard and William M. Dehn. DOI: 10.15227/orgsyn.001.0029. | Organic Syntheses | |
| BENZIMIDAZOLE | Preparation of BENZIMIDAZOLE. Submitted by E. C. Wagner and W. H. Millett. DOI: 10.15227/orgsyn.019.0012. | Organic Syntheses | |
| BENZOANNELATION OF KETONES: 3,4-CYCLODODECENO-1-METHYLBENZENE (Benzocyclododecene, 5,6,7,8,9,10,11,12,13,14-decahydro-2-methyl-) | Preparation of Benzocyclododecene, 5,6,7,8,9,10,11,12,13,14-decahydro-2-methyl-. Submitted by Marcus A. Tius and G. S. Kamali Kannangara1. DOI: 10.15227/orgsyn.071.0158. | Organic Syntheses | |
| BENZOCYCLOBUTENONE BY FLASH VACUUM PYROLYSIS (Bicyclo[4.2.0]octa-1,3,5-trien-7-one) | Preparation of Bicyclo[4.2.0]octa-1,3,5-trien-7-one. Submitted by Peter Schiess, Ppatibha V. Barve, Franz E. Dussy, and Andreas Pfiffner1. DOI: 10.15227/orgsyn.072.0116. | Organic Syntheses | |
| BENZOCYCLOPROPENE (Bicyclo [4.1.0]hepta-1,3,5-triene) | Preparation of Bicyclo [4.1.0]hepta-1,3,5-triene. Submitted by W. E. Billups1, A. J. Blakeney, and W. Y. Chow1. DOI: 10.15227/orgsyn.055.0012. | Organic Syntheses | |
| BENZOFURAZAN OXIDE (Benzofurazan 1-oxide) | Preparation of Benzofurazan 1-oxide. Submitted by F. B. Mallory1. DOI: 10.15227/orgsyn.037.0001. | Organic Syntheses | |
| BENZOGUANAMINE (s-Triazine, 2,4-diamino-6-phenyl-) | Preparation of s-Triazine, 2,4-diamino-6-phenyl-. Submitted by J. K. Simons and M. R. Saxton1. DOI: 10.15227/orgsyn.033.0013. | Organic Syntheses | |
| BENZOHYDROL | Preparation of BENZOHYDROL. Submitted by F. Y. Wiselogle and H. Sonneborn, III. DOI: 10.15227/orgsyn.008.0024. | Organic Syntheses | |
| BENZOHYDROXAMIC ACID | Preparation of BENZOHYDROXAMIC ACID. Submitted by C. R. Hauser and W. B. Renfrow, Jr. DOI: 10.15227/orgsyn.019.0015. | Organic Syntheses | |
| BENZOIC ANHYDRIDE | Preparation of BENZOIC ANHYDRIDE. Submitted by H. T. Clarke and E. J. Rahrs. DOI: 10.15227/orgsyn.003.0021. | Organic Syntheses | |
| BENZOIN | Preparation of BENZOIN. Submitted by Roger Adams and C. S. Marvel. DOI: 10.15227/orgsyn.001.0033. | Organic Syntheses | |
| BENZOIN ACETATE | Preparation of BENZOIN ACETATE. Submitted by B. B. Corson and N. A. Saliani. DOI: 10.15227/orgsyn.012.0001. | Organic Syntheses | |
| BENZOPHENONE | Preparation of BENZOPHENONE. Submitted by C. S. Marvel and W. M. Sperry. DOI: 10.15227/orgsyn.008.0026. | Organic Syntheses | |
| BENZOPHENONE OXIME | Preparation of BENZOPHENONE OXIME. Submitted by Arthur Lachman. DOI: 10.15227/orgsyn.010.0010. | Organic Syntheses | |
| BENZOPINACOL Rearrangement | Preparation of BENZOPINACOL. Submitted by W. E. Bachmann. DOI: 10.15227/orgsyn.014.0008. | Organic Syntheses | |
| BENZOYLACETANILIDE (Acetanilide, 2-benzoyl-) | Preparation of Acetanilide, 2-benzoyl-. Submitted by C. F. H. Allen and W. J. Humphlett1. DOI: 10.15227/orgsyn.037.0002. | Organic Syntheses | |
| BENZOYLACETANILIDE (Acetanilide, α-benzoyl-) | Preparation of Acetanilide, α-benzoyl-. Submitted by Charles J. Kibler and A. Weissberger. DOI: 10.15227/orgsyn.025.0007. | Organic Syntheses | |
| BENZOYLCHOLINE IODIDE AND CHLORIDE (Choline, chloride benzoate, and Choline, iodide benzoate) | Preparation of Choline, chloride benzoate, and Choline, iodide benzoate. Submitted by A. H. Ford-Moore1. DOI: 10.15227/orgsyn.030.0010. | Organic Syntheses | |
| BENZOYL CYANIDE (Glyoxylonitrile, phenyl-) | Preparation of Glyoxylonitrile, phenyl-. Submitted by T. S. Oakwood and C. A. Weisgerber. DOI: 10.15227/orgsyn.024.0014. | Organic Syntheses | |
| BENZOYL DISULFIDE | Preparation of BENZOYL DISULFIDE. Submitted by Robert L. Frank and James R. Blegen1. DOI: 10.15227/orgsyn.028.0016. | Organic Syntheses | |
| BENZOYLENE UREA (2,4(1,3)-Quinazolinedione) | Preparation of 2,4(1,3)-Quinazolinedione. Submitted by N. A. Lange and F. E. Sheibley. DOI: 10.15227/orgsyn.017.0016. | Organic Syntheses |
