Reactions

1,033–1,056 of 3,374

1. Catalytic asymmetric acylation of alcohols using a chiral 1,2-diamine derived from (S)-proline: (1S,2S)-trans-1-benzoyloxy-2-bromocyclohexane Org. Synth. Vol. 83, p. 70 · Terakado and Oriyama
2. Catalytic asymmetric addition of an in-situ prepared arylzinc to cyclohexanecarboxaldehyde: (R)-(+)-α-cyclohexyl-3-methoxy-benzenemethanolAddition Org. Synth. Vol. 87, p. 68 · DeBerardinis et al.
3. Catalytic asymmetric allylation reactions: (S)-1-(phenylmethoxy)-4-penten-2-ol Org. Synth. Vol. 75, p. 12 · Keck and Krishnamurthy
4. Catalytic asymmetric synthesis of nitroaldols using a lanthanum-lithium-BINOL complex: (2S,3S)-2-nitro-5-phenyl-1,3-pentanediolCondensation Org. Synth. Vol. 78, p. 14 · Sasaia et al.
5. Catalytic enantioselective addition of dialkylzincs to aldehydes using (2S)-(−)-3-exo-(dimethylamino)isoborneol [(2S)-DAIB]: (S)-1-phenyl-1-propanolAddition Org. Synth. Vol. 79, p. 139 · Kitamura et al.
6. Catalytic enantioselective addition of terminal alkynes to aldehydes: preparation of (S)-(-)-1,3-diphenyl-2-propyn-1-ol and (S)-(-)-4-methyl-1-phenyl-2-pentyn-1,4-diolAddition Org. Synth. Vol. 85, p. 118 · Takita et al.
7. Catalytic enantioselective borane reduction of benzyl oximes: preparation of (S)-1-pyridin-3-yl-ethylamine bis hydrochlorideReduction Org. Synth. Vol. 87, p. 36 · Huang and Ortiz-Marciales
8. Catalytic Intramolecular Friedel-Crafts Reaction of Benzyl Meldrum's Acid Derivatives: Preparation of 5,6-Dimethoxy-2-Methyl-1-IndanoneElectrophilic aromatic substitution Org. Synth. Vol. 89, p. 115 · Lou et al.
9. Catalytic osmium tetroxide oxidation of olefins: cis-1,2-cyclohexanediolOxidation Org. Synth. Coll. Vol. 6, p. 342; Vol. 58, p. 43 · VanRheenen et al.
10. Catalytic reduction of amides to amines with hydrosilanes using a triruthenium carbonyl cluster as the catalystReduction Org. Synth. Vol. 82, p. 188 · Motoyama et al.
11. Catechol Org. Synth. Coll. Vol. 1, p. 149; Vol. 3, p. 28 · Dakin
12. Cellobiose Org. Synth. Coll. Vol. 2, p. 122; Vol. 17, p. 34 · Braun
13. α-Cellobiose octaacetate Org. Synth. Coll. Vol. 2, p. 124; Vol. 17, p. 36 · Braun
14. Cetylmalonic ester Org. Synth. Coll. Vol. 4, p. 141; Vol. 34, p. 13 · Floyd and Miller
15. Chain elongation of alkenes via gem-dihalocyclopropanes: 2-bromo-3,3-diphenyl-2-propen-1-yl acetate Org. Synth. Coll. Vol. 6, p. 187; Vol. 56, p. 32 · Sandler
16. Chelidonic acid Org. Synth. Coll. Vol. 2, p. 126; Vol. 17, p. 40 · Riegel and Zwilgmeyer
17. Chiral (acyloxy)borane complex-catalyzed asymmetric Diels-Alder reaction: (1R)-1,3,4-trimethyl-3-cyclohexene-1-carboxaldehyde Org. Synth. Coll. Vol. 9, p. 722; Vol. 72, p. 86 · Furuta et al.
18. Chiral 1,3-oxathiane from (+)-pulegone: hexahydro-4,4,7-trimethyl-4H-1,3-benzoxathiin Org. Synth. Coll. Vol. 8, p. 302; Vol. 65, p. 215 · Eliel et al.
19. Chiral lithium amide base desymmetrization of a ring fused imide: formation of (3aS,7aS)-2-[2-(3,4-dimethoxyphenyl)-ethyl]-1,3-dioxo-octahydro-isoindole-3a-carboxylic acid methyl ester Org. Synth. Vol. 84, p. 306 · Rodeschini et al.
20. Chiral media for asymmetric solvent inductions. (S,S)-(+)-1,4-Bis(dimethylamino)-2,3-dimethoxybutane from (R,R)-(+)-diethyl tartrate Org. Synth. Coll. Vol. 7, p. 41; Vol. 61, p. 24 · Seebach et al.
21. α-Chlorination of carboxylic acids mediated by chlorosulfonic acid: ε-benzoylamino-α-chlorocaproic acid Org. Synth. Coll. Vol. 6, p. 90; Vol. 59, p. 20 · Ogata et al.
22. 4-Chlorination of electron-rich benzenoid compounds: 2,4-dichloromethoxybenzene Org. Synth. Coll. Vol. 8, p. 167; Vol. 67, p. 222 · Smith et al.
23. α-Chloro enamines, reactive intermediates for synthesis: 1-chloro-N,N,2-trimethylpropenylamine Org. Synth. Coll. Vol. 6, p. 282; Vol. 59, p. 26 · Haveaux et al.
24. 1-Chloro-(2S,3S)-dihydroxycyclohexa-4,6-diene Org. Synth. Vol. 76, p. 77 · Hudlicky et al.