Reactions

3,025–3,048 of 3,374

1. Synthesis of 1,1-dimethylethyl (S)-4-formyl-2,2-dimethyl-3-oxazolidinecarboxylate by oxidation of the alcoholOxidation Org. Synth. Vol. 77, p. 64 · Dondoni and Perrone
2. Synthesis of 1,2:4,5-di-O-isopropylidene-D-erythro-2,3-hexodiulo-2,6-pyranose. A highly enantioselective ketone catalyst for epoxidationOxidation Org. Synth. Vol. 80, p. 1 · Tu et al.
3. Synthesis of 1,2:5,6-dianhydro-3,4-O-isopropylidene-L-mannitol Org. Synth. Vol. 81, p. 140 · Nugiel et al.
4. Synthesis of 1,3-dienes from alkynes and ethylene: acetic acid 2-methylene-3-phenethylbut-3-enyl ester Org. Synth. Vol. 81, p. 1 · Mori et al.
5. Synthesis of 1,3-Dimethyl-3-(p-tolyl)-1H-pyrrolo[3,2-c]pyridin-2(3H)-one by Cu(II)-Mediated Direct Oxidative CouplingCross-coupling Org. Synth. Vol. 91, p. 221 · Dey and Kündig*
6. Synthesis of 1,4-diketones from silyl enol ethers and nitroolefins: 2-(2-oxopropyl)cyclohexanone Org. Synth. Coll. Vol. 7, p. 414; Vol. 60, p. 117 · Miyashita et al.
7. Synthesis of 2-[3,3'-di-(tert-butoxycarbonyl)-aminodipropylamine]-4,6,-dichloro-1,3,5-triazine as a monomer and 1,3,5-[tris-piperazine]-triazine as a core for the large scale synthesis of melamine (triazine) dendrimers Org. Synth. Vol. 86, p. 141 · Chouai et al.
8. Synthesis of 2-aryl pyridines by palladium-catalyzed direct arylation of pyridine N-oxides Org. Synth. Vol. 88, p. 22 · Campeau and Fagnou
9. Synthesis of 2-arylindole-4-carboxylic amides: [2-(4-fluorophenyl)-1H-indol-4-yl]-1-pyrrolidinylmethanone Org. Synth. Vol. 86, p. 92 · Kuethe and Beutner
10. Synthesis of 2-chloroacrolein diethyl acetal Org. Synth. Vol. 83, p. 184 · Kvernenes and Sydnes
11. Synthesis of 2-substituted biaryls via Cu/Pd-catalyzed decarboxylative cross-coupling of 2-substituted potassium benzoates: 4-methyl-2'-nitrobiphenyl and 2-acetyl-4'-methylbiphenylCross-coupling Org. Synth. Vol. 85, p. 196 · Gooßen et al.
12. Synthesis of 2-substituted naphthalenediol derivatives using chromium carbene complexes: 1-acetoxy-2-butyl-4-methoxynaphthalene Org. Synth. Coll. Vol. 9, p. 1; Vol. 71, p. 72 · Timko and Yamashita
13. Synthesis of 2,3-Disubstituted Benzofurans by the Palladium-Catalyzed Coupling of 2-Iodoanisoles and Terminal Alkynes, Followed by Electrophilic Cyclization: 3-Iodo-2-phenylbenzofuranCross-coupling Org. Synth. Vol. 91, p. 283 · Yao et al.
14. Synthesis of 2,3-disubstituted indoles via palladium-catalyzed annulation of internal alk ynes: 3-methyl-2-(trimethylsilyl)indoleCyclization Org. Synth. Vol. 88, p. 377 · Chen et al.
15. Synthesis of 2'-deoxyribonucleosides: β-3',5'-di-O-benzoylthymidine Org. Synth. Vol. 77, p. 162 · Prudhomme et al.
16. Synthesis of 2α-benzyloxy-8-oxabicyclo[3.2.1]oct-6-en-3-one by [4 + 3] cycloadditionCycloaddition Org. Synth. Vol. 83, p. 61 · Vidal-Pascual et al.
17. Synthesis of 3-pyridylboronic acid and its pinacol ester. Application of 3-pyridylboronic acid in Suzuki coupling to prepare 3-pyridin-3-ylquinolineCross-coupling Org. Synth. Vol. 81, p. 89 · Li et al.
18. Synthesis of 4-, 5-, and 6-methyl-2,2'-bipyridine by a Negishi cross-coupling strategy: 5-methyl-2,2'-bipyridineCross-coupling Org. Synth. Vol. 78, p. 51 · Smith et al.
19. Synthesis of 4-(2-bromo-2-propenyl)-4-methyl-γ-butyrolactone by the reaction of ethyl levulinate with (2-bromoallyl)diisopropoxyborane prepared by haloboration of allene Org. Synth. Vol. 75, p. 129 · Hara and Suzuki
20. Synthesis of 4-triisopropylsilyl-3-butyn-2-ol by asymmetric transfer hydrogenationReduction Org. Synth. Vol. 84, p. 120 · Marshall et al.
21. Synthesis of 4,5-dimethyl-1,3-dithiol-2-one Org. Synth. Vol. 86, p. 333 · Chandrasekaran and Donahue
22. Synthesis of 4,5-Disubstituted 2-aminothiazoles from α,β-Unsaturated Ketones: Preparation of 5-Benzyl-4-methyl-2-aminothiazolium Hydrochloride Salt Org. Synth. Vol. 91, p. 185 · Gómez and Martín-Matute*
23. Synthesis of 5-bromoisoquinoline and 5-bromo-8-nitroisoquinoline Org. Synth. Vol. 81, p. 98 · Browna and Gouliaevb
24. Synthesis of 6,9,12,15,18-pentamethyl-1,6,9,12,15,18-hexahydro(C60-Ih)[5,6]fullerene Org. Synth. Vol. 83, p. 80 · Matsuo et al.