Reactions

745–768 of 3,374

1. Arylbenzenes: 3,4-dichlorobiphenyl Org. Synth. Coll. Vol. 5, p. 51; Vol. 49, p. 44 · Hey and Perkins
2. Arylureasi. Cyanate METHODp-bromophenylurea Org. Synth. Coll. Vol. 4, p. 49; Vol. 31, p. 8 · Kurzer
3. Arylureasii. Urea METHODp-ethoxyphenylurea Org. Synth. Coll. Vol. 4, p. 52; Vol. 31, p. 11
4. (3R,7aS)-3-(trichloromethyl)tetrahydropyrrolo[1,2-C]oxazol-1(3H)-one: an air and moisture stable reagent for the synthesis of optically active α-branched prolines Org. Synth. Vol. 86, p. 262 · III et al.
5. (+)-(7aS)-7a-methyl-2,3,7,7a-tetrahydro-1 H-indene-1,5-(6H-dione Org. Synth. Coll. Vol. 7, p. 363; Vol. 63, p. 26 · Hajos and Parrish
6. (+)-(2R,8aS)-10-(camphorylsulfonyl)oxaziridine Org. Synth. Coll. Vol. 8, p. 104; Vol. 69, p. 158 · Towson et al.
7. asym-dimethylurea Org. Synth. Coll. Vol. 4, p. 361; Vol. 32, p. 61 · Kurzer
8. Asymmetric alcoholysis of meso-anhydrides mediated by alkaloids Org. Synth. Vol. 82, p. 120 · Bolm et al.
9. Asymmetric catalytic glyoxylate-ene reaction: methyl (2R)-2-hydroxy-4-phenyl-4-pentenoate Org. Synth. Coll. Vol. 9, p. 596; Vol. 71, p. 14 · Mikami et al.
10. Asymmetric epoxidation of trans-β-methylstyrene and 1-phenylcyclohexene using a D-fructose-derived ketone: (R,R)-trans-β-methylstyrene oxide and (R,R)-1-phenylcyclohexene oxideOxidation Org. Synth. Vol. 80, p. 9 · Wang et al.
11. Asymmetric hydroboration of 5-substituted cyclopentadienes: synthesis of methyl (1 R,5R)-5-hydroxy-2-cyclopentene-1-acetateAddition Org. Synth. Coll. Vol. 7, p. 339; Vol. 63, p. 44 · Partridge et al.
12. Asymmetric hydrogenation of 3-oxo carboxylates using BINAP-ruthenium complexes: (R)-(−)-methyl 3-hydroxybutanoateReduction Org. Synth. Coll. Vol. 9, p. 589; Vol. 71, p. 1 · Kitamura et al.
13. Asymmetric hydrogenation of allylic alcohols using BINAP-ruthenium complexes: (S)-(−)-citronellolReduction Org. Synth. Coll. Vol. 9, p. 169; Vol. 72, p. 74 · Takaya et al.
14. Asymmetric hydrogenation of ketopantoyl lactone: D-(−)-pantoyl lactoneReduction Org. Synth. Coll. Vol. 7, p. 417; Vol. 63, p. 18 · Ojima et al.
15. Asymmetric rearrangement of allylic trichloroacetimidates: preparation of (S)-2,2,2-trichloro-N-(1-propylallyl)acetamideRearrangement Org. Synth. Vol. 82, p. 134 · Anderson et al.
16. Asymmetric reduction of α,β-acetylenic ketones with B-3-pinanyl-9-borabicyclo[3.3.1]nonane: (R)-(+)-1-octyn-3-olReduction Org. Synth. Coll. Vol. 7, p. 402; Vol. 63, p. 57 · Midland and Graham
17. Asymmetric syntheses using the SAMP-/RAMP-hydrazone method: (S)-(+)-4-methyl-3-heptanone Org. Synth. Coll. Vol. 8, p. 403; Vol. 65, p. 183 · Enders et al.
18. Asymmetric synthesis of (M)-2-hydroxymethyl-1-(2-hydroxy-4,6-dimethylphenyl)naphthalene via a configurationally unstable biaryl lactone Org. Synth. Vol. 79, p. 72 · Bringmann et al.
19. Asymmetric synthesis of 4,4-dialkylcyclohexenones from chiral bicyclic lactams: (R)-4-ethyl-4-allyl-2-cyclohexen-1-one Org. Synth. Coll. Vol. 8, p. 241; Vol. 69, p. 55 · Meyers and Berney
20. Asymmetric synthesis of diethyl (R)-(−)-(1-amino-3-methylbutyl)phosphonate Org. Synth. Vol. 75, p. 19 · Smith et al.
21. Asymmetric synthesis of N-tert-butoxycarbonyl α-amino acids. Synthesis of (5S,6R)-4-tert-butoxycarbonyl-5,6-diphenylmorpholin-2-one Org. Synth. Vol. 80, p. 18 · Williams et al.
22. Asymmetric synthesis of trans-2-aminocyclohexanecarboxylic acid derivatives from pyrrolobenzodiazepine-5,11-diones: (1S,2S)-2-(N-tosylamino)cyclohexanecarboxylic acid Org. Synth. Coll. Vol. 9, p. 698; Vol. 73, p. 174 · Schultz and Alva
23. ASYMMETRIC SYNTHESIS OF α-AMINO ACIDS BY THE ALKYLATION OF PSEUDOEPHEDRINE GLYCINAMIDE: L-ALLYLGLYCINE AND N-BOC-L-ALLYLGLYCINE (Acetamide, 2-amino-N-(2-hydroxy-1-methyl-2-phenylethyl)-N-methyl-, [R-(R,R)]-, 4-Pentenoic acid, 2-amino-, (R)- and 4-Pentenoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, (R)-)) Org. Synth. Vol. 76, p. 57 · Myers and Gleason
24. Atrolactic acid Org. Synth. Coll. Vol. 4, p. 58; Vol. 33, p. 7 · Eliel and Freeman