Organic Syntheses, Collective Volume 6ISBN: 978-0-471-85243-8
Hardcover
1232 pages
May 1988
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Acylamidoalkyl Acetophenones from Substituted Phenethylamines: 2-(2-Acetamidoethyl)-4,5-dimethoxyacetophenone (56, 3)
Thiol Protection with the Acetamidomethyl Group: S-Acetamidomethyl-l-cysteine Hydrochloride (59, 190)
Acetic Formic Anhydride (50, 1)
Acetone Hydrazone (50, 3)
Preparation of Hydrazones: Acetophenone Hydrazone (50, 102)
3β-Acetoxy-5α-cyanocholestan-7-one (52, 100)
p-Acetyl-α-bromohydrocinnamic Acid (51, 1)
α,β-Dehydrogenation of β-Dicarbonyl Compounds by Selenoxide Elimination: 2-Acetyl-2-cyclohexen-1-one (59, 58)
2-Acetyl-1,3-cyclopentanedione (52, 1)
3-Acetyl-2,4-dimethylfuran (53, 1)
2-Acetyl-6-methoxynaphthalene (53, 5)
Copper Catalyzed Arylation of β-Dicarbonyl Compounds: 2-(1-Acetyl-2-oxopropyl)benzoic Acid (58, 52)
5-Acetyl- 1,2,3,4,5-pentamethylcyclopentadiene (56, 1)
2-Adamantanecarbonitrile (57, 8)
Tertiary Alcohols from Hydrocarbons by Ozonation on Silica Gel: 1-Adamantanol (59, 176)
Adamantanone (53, 8)
Enone Reduction-Enolate Alkylation Sequence: 2-Allyl-3-methylcyclohexanone (56, 52)
Preparation of N-Aminoaziridines: trans-1-Amino-2,3-diphenylaziridine, 1-Amino-2-phenylaziridine, and 1-Amino-2-phenylaziridinium Acetate (55, 114)
Reduction of Ketones by Use of the Tosylhydrazone Derivatives: Androstan-17β-Ol (52, 122)
Aldehydes from 4,4-Dimethyl-2-oxazoline and Grignard Reagents: o-Anisaldehyde (54, 42)
[18]Annulene (54, 1)
Azetidine (53, 13)
Azoethane (52, 11)
Diels-Alder Addition of Perchlorobenzyne: Benzobarrelene (59, 71)
Benzocyclopropene (55, 12)
α-Chlorination of Carboxylic Acids Mediated by Chlorosulfonic Acid: &phis;-Benzoylamino-α-chlorocaproic Acid (59, 20)
1-N-Acylamino-1,3-dienes from 2,4-pentadienoic Acids by the Curtius Rearrangement: Benzyl trans-1,3-Butadiene-1-carbamate (59, 1)
Benzyl Chloromethyl Ether (52, 16)
1-Benzylindole (54, 58)
N-Alkylindoles from the Alkylation of Sodium Indolide in Hexamethylphosphoric Triamide: 1-Benzylindole (54, 60)
3-Alkylated and 3-Acylated Indoles from a Common Precursor: 3-Benzylindole and 3-Benzoylindole (56, 8)
Alkylation of Isoquinolines via 2-Benzoyl-1,2-dihydroisoquinaldonitriles: 1-Benzylisoquinoline (56, 19)
The Formation and Alkylation of Specific Enolate Anions from an Unsymmetrical Ketone: 2-Benzyl-2-methylcyclohexanone and 2-Benzyl-6-methylcyclohexanone (52, 39)
Sulfide Synthesis: Benzyl Sulfide (58, 138)
Bicyclo[1.1.0]butane (51, 55)
Boranes in Functionalization of Dienes to Cyclic Ketones: Bicyclo[3.3.1]nonan-9-one (58, 24)
Bicyclo[3.2.1]octan-3-one (51, 60)
Bicyclo[2.1.0]pent-2-ene (55, 15)
Dehydroxylation of Phenols; Hydrogenolysis of Phenolic Ethers: Biphenyl (51, 82)
Controlled-Potential Electrolytic Reduction: 1,1-Bis(bromomethyl)cyclopropane (52, 22)
Bis(trifluoromethyl)diazomethane (50, 6)
Bis[2,2,2-trifluoro-1-phenyl-1-(trifluoromethyl)ethoxy] Diphenyl Sulfurane (57, 22)
Acyloin Condensation in which Chlorotrimethylsilane is Used as a Trapping Agent: 1,2-Bis(trimethylsilyloxy)cyclobutene and 2-Hydroxycyclobutanone (57, 1)
2-Bornene (51, 66)
Selective α-Bromination of an Aralkyl Ketone with Phenyltrimethylammonium Tribromide: 2-Bromoacetyl-6-methoxynaphthalene and 2,2-Dibromoacetyl-6-methoxynaphthalene (53, 111)
Mercury(II) Oxide-Modified Hunsdiecker Reaction: 1-Bromo-3-chlorocyclobutane (51, 106)
para-Bromination of Aromatic Amines: 4-Bromo-N,N-dimethyl-3-(trifluoromethyl)aniline (55, 20)
Bromohydrins from Alkenes and N-Bromosuccinimide in Dimethyl Sulfoxide; erythro-2-Bromo-1,2-diphenylethanol (59, 16)
Chain Elongation of Alkenes via gem-Dihalocyclopropanes: 2-Bromo-3,3-diphenyl-2-propen-1-yl acetate (56, 32)
2-Bromohexanoyl Chloride (55, 27)
1-Bromo-3-methyl-2-butanone (55, 24)
trans, trans-1,3-Butadiene-1,4-diyl Diacetate (50, 24)
A New Reagent for tert-Butoxycarbonylation: 2-tert-Butoxycarbonyloxyimino-2-phenylacetonitrile (59, 95)
tert-Butoxycarbonyl-l-proline (53, 25)
tert-Butyl Azidoformate (50, 9; 57, 122)
tert-Butylcyanoketene (55, 32)
cis-4-tert-Butylcyclohexanol (50, 13)
Polymeric Carbodiimide. Moffat Oxidation: 4-tert-Butylcyclohexanone (56, 99)
Oxidation of Alcohols by Methyl Sulfide- N-Chlorosuccinimide- Triethylamine: 4-tert-Butylcyclohexanone (58, 122)
2-tert-Butyl-1,3-diaminopropane (53, 21)
Photochemical Ring-Contraction of 2-Ethoxypyrrolin-5-ones to Cyclopropanone Derivatives: tert-Butyl N-(1-Ethoxycyclopropyl)carbamate (59, 132)
Phase-Transfer Hofmann Carbylamine Reaction: tert-Butyl Isocyanide (55, 96)
Sulfide Synthesis in Preparation of Unsymmetrical Dlalkyl Disulfides: sec-Butyl Isopropyl Disulfide (58, 147)
3-Butyl-2-Methylhept-1-en-3-ol (52, 19)
Monoalkylation of α,β-Unsaturated Ketones via Metalloenamines: 1-Butyl-10-methyl-Δ1(9)-2-octalone (57, 69)
β-Diketones from Methyl Alkyl Ketones: 3-n-Butyl-2,4-pentanedione (51, 90)
Secondary and Tertiary Alkyl Ketones from Carboxylic Acid Chlorides and Lithium Phenylthio(alkyl)cuprate Reagents: tert-Butyl Phenyl Ketone (55, 122)
Removal of Nα-Benzyloxycarbonyl Groups from Sulfur-Containing Peptides by Catalytic Hydrogenation in Liquid ammonia: O-tert-Butyl-L-seryl-S-tert-butyl-l-cysteine tert-Butyl Ester (59, 159)
Esterification of Hindered Alcohols: tert-Butyl p-Toluate (51, 96)
Peptide Syntheses Using N-Ethyl-5-phenylisoxazolium-3-sulfonate:
Carbobenzoxy-L-asparaginyl-L-leucine Methyl Ester and N-Carbobenzoxy-3-hydroxy-L-prolylglycylglycine Ethyl Ester (56, 88)
Carbonyl Cyanide (51, 70)
3-Chlorocyclobutanecarboxylic Acid (51, 73)
(z)-4-Chloro-4-hexenyl Trifluoroacetate (57, 26)
m-Chloroperbenzoic Acid (50, 15)
3-(4-Chlorophenyl)-5-(4-Methoxyphenyl)Isoxazole (55, 39)
α-Chloro Enamines, Reactive Intermediates for Synthesis: 1-Chloro-N,N,2-trimethylpropenylamine (59, 26)
Modified Clemmensen Reduction: Cholestane (53, 86)
Conjugate Reduction of α,β-Unsaturated p-Toluenesulfonylhydrazones to Alkenes with Catecholborane: 5β-Cholest-3-ene (59, 42)
5β-Cholest-3-Ene-5-Acetaldehyde (54, 71)
18-Crown-6 (57, 30)
Cinnamonitrile (50, 18)
Preparation of Cyano Compounds Using Alkylaluminum Intermediates: 1-Cyano-6-methoxy-3,4-Dihydronaphthalene (52, 96)
Cyclobutadieneiron Tricarbonyl (50, 21)
Aldehydes from acid Chlorides by Reduction of Ester-mesylates with Sodium Borohydride: Cyclobutanecarboxaldehyde (51, 11)
Cyclic Ketones from 1,3-Dithiane: Cyclobutanone (51, 76)
Cyclobutanone from Methylenecyclopropane via Oxaspiropentane (57, 36)
Cyclobutanone Via Solvolytic Cyclization (54, 84)
One-carbon Ring Expansion of Cycloalkanones to Conjugated Cycloalkenones: 2-Cyclohepten-1-one (59, 113)
Nitriles from Ketones: Cyclohexanecarbonitrile (58, 101)
Aldehydes from Olefins: Cyclohexanecarboxaldehyde (57, 11)
Catalytic Osmium Tetroxide Oxidation of Olefins: cis-1,2-Cyclohexanediol (58, 43)
Stereoselective Hydroxylation with Thallium(i) Acetate and Iodine: trans- and cis-1,2-Cyclohexanediols (59, 169)
Cleavage of Methyl Ethers with Iodotrimethylsilane: Cyclohexanol from Cyclohexyl Methyl Ether (59, 35)
Preparation of α,β-Unsaturated Aldehydes via the Wittig Reaction: Cyclohexylideneacetaldehyde (53, 104)
Cyclopropenone (57, 41)
Cyclopropyldiphenylsulfonium Tetrafluoroborate (54, 27)
Ring Contraction via a Favorskii-Type Rearrangement: Cycloundecanone (56, 107)
Hydrogenation of Aromatic Nuclei: 1-Decalol (51, 103)
Oxidation with the Chromium Trioxide-Pyridine Complex Prepared in situ: 1-Decanal (55, 84)
Reduction of Alkyl Halides and Tosylates with Sodium Cyanoborohydride in Hexamethylphosphoric Triamide (HMPA): A. 1-Iododecane to n-Decane B. 1-Dodecyl Tosylate to n-Dodecane (53, 107)
Diamantane: Pentacyclo[7.3.1.14,12.02,7.06,11]tetradecane (53, 30)
Macrocyclic Diimines: 1,10-dlazacyclöCtadecane (54, 88)
Dlazoacetophenone (53, 35)
2-diazocycloalkanones: 2-diazocyclohexanone (51, 86)
2-diazopropane (50, 27)
Macrocyclic Polyethers: Dibenzo-18-crown-6 Polyether and Dicyclohexyl-18-crown-6 Polyether (52, 66)
1,2-Diaroylcyclopropanes: trans-1,2-Dibenzoylcyclopropane (52, 33)
α,???-Dibromodibenzyl Sulfone (50, 31)
Phosphine-Nickel Complex Catalyzed Cross-Coupling of Grignard Reagents with Aryl and Alkenyl Halides: 1,2-Dibutylbenzene (58, 127)
Oxidation with Bis(Salicylidene)ethylenediiminocobalt(II) (Salcomine); 2,6-Di-tert-butyl-p-benzoquinone (57, 78)
Diazo Transfer by Means of Phase-transfer Catalysis: Di-tert-Butyl Diazomalonate (59, 66)
Di-tert-butyl Dicarbonate (57, 45)
cis-3,4-Dichlorocyclobutene (50, 36)
cis-Dichloroalkanes from Epoxides: cis-1,2-Dichlorocyclohexane (58, 64)
2,3-Dicyanobutadiene as a Reactive Intermediate by in situ Generation from 1,2-Dicyanocyclobutene: 2,3-Dicyano-1,4,4a,9a-tetrahydrofluorene (58, 67)
Dideuteriodiazomethane (53, 38)
Diethylaluminum cyanide (52, 90)
Diethylaminosulfur trifluoride (57, 50)
Diethyl tert-Butylmalonate (50, 38)
2-Trimethylsilyloxy-1,3-butadiene as a Reactive Diene: Diethyl trans-4-Trimethylsilyloxy-4-cyclohexene-1,2-dicarboxylate (58, 163)
Diethyl 2-(Cyclohexylamino)vinylphosphonate (53, 44)
Radical Anion Arylation: Diethyl Phenylphosphonate (58, 134)
Diethyl trans-δ4-Tetrahydrophthalate (50, 43)
Homogeneous Catalytic Hydrogenation: Dihydrocarvone (53, 63)
trans-1,2-Dihydrophthalic Acid (50, 50)
5,6-Dihydro-2H-pyran-2-one and 2H-Pyran-2-One (56, 49)
2,4-Dimethoxybenzonitrile (50, 52)
Biaryls from Simple Arenes via Organotellurium Intermediates; 4,4-Dimethoxy-1,1-Biphenyl (57, 18)
6,7-Dimethoxy-3-Isochromanone (55, 45)
Regioselective Mannich Condensation with Dimethyl(methylene)ammonium Trifluoroacetate: 1-Dimethylamino-4-methyl-3-pentanone (59, 153)
Directed Lithiation of Aromatic Compounds: (2-Dimethylamino-5-methylphenyl)diphenylcarbinol (53, 56)
Use of Dipotassium Nitrosodisulfonate (fremys Salt): 4,5-Dimethyl-o-Benzoquinone (52, 88)
1,2-Dimethylcyclobutenes by Reductive Ring-Contraction of Sulfolanes: cis-7,8-Dimethylbicyclo[4.2.0]oct-7-Ene (57, 53)
4,4-Dimethyl-1,1-biphenyl (55, 48)
N,N-Dimethyl-5β-cholest-3-Ene-5-acetamide (54, 77)
Conversion of Esters to Amides with Dimethylaluminum Amides: N,N-Dimethylcyclohexanecarboxamide (59, 49)
4,4-Dimethyl-2-Cyclohexen-1-one (53, 48)
Reductive Amination with Sodium Cyanoborohydride: N,N- Dimethylcyclohexylamine (52, 124)
N,N-Dimethyldodecylamine Oxide (50, 56)
Dimethyl Nitrosuccinate (57, 60)
Dimethyl 2,3-Pentadienedioate (57, 62)
Allylically Transposed Amines from Allylic Alcohols; 3,7-Dimethyl-1,6-octadien-3-amine (58, 4)
Bicyclic Ketones for The Synthesis of Tropinoids: 2α,4α-Dimethyl-8-oxabicyclo[3.2.1]oct-6-en-3-one (58, 17)
2,2-Dimethyl-4-Phenylbutyric Acid (50, 58)
Cyclopentenones from α,α-Dibromoketones and Enamines: 2,5-Dimethyl-3-phenyl-2-cyclopenten-1-one (58, 56)
Alkylations of Aldehydes via Reaction of the Magnesioenamine Salt of an Aldehyde: 2,2-Dimethyl-3-phenylpropionaldehyde (54, 46)
3,5-Dinitrobenzaldehyde (53, 52)
2,3-Diphenyl-1,3-butadiene (50, 62)
Reagents for Synthesis of Organoselenium Compounds: Diphenyl Diselenide and Benzeneselenenyl Chloride (59, 141)
Aromatic Hydrocarbons from Aromatic Ketones and Aldehydes: 1,1-Diphenylethane (55, 7)
Nucleophilic α-sec-Aminoalkylation: 2-(Diphenylhydroxymethyl)pyrrolidine (58, 113)
Diphenylketene (52, 36)
Alkenes via Hofmann Elimination: Use of Ion-Exchange Resin for Preparation of Quaternary Ammonium Hydroxides: Diphenylmethyl Vinyl Ether (55, 3)
2,3-Diphenylvinylene Sulfone (50, 65)
1,3-Dithiane (50, 72)
2,2-Dithienyl Sulfide (50, 75)
Selective Epoxidation of Terminal Double Bonds: 10, 11-Epoxyfarnesyl Acetate (56, 112)
1-Ethoxy-1-butyne (57, 65)
Demethylation of Methyl Aryl Ethers: 4-Ethoxy-3-hydroxybenzaldehyde (56, 44)
Carbine Generation by α-Elimination with Lithium 2,2,6,6-Tetramethylpiperidide: 1-Ethoxy-2-p-tolylcyclopropane (58, 37)
Esterification of Carboxylic Acids with Trialkyloxonium Salts; Ethyl and Methyl 4-Acetoxybenzoates (56, 59)
ortho-Alkylation of Anilines: Ethyl 4-Amino-3-Methylbenzoate (56, 15)
Ethyl 5β-Cholest-3-ene-5-acetate (54, 74)
Free-Radical Cyclization: Ethyl 1-Cyano-2-Methylcyclohexanecarboxylate (55, 57)
2,2-(Ethylenedithio)cyclohexanone (54, 37)
A General Synthesis of 4-Isoxazolecarboxylic Esters: Ethyl 3-Ethyl-5-methyl-4-isoxazolecarboxylate (53, 59)
3-Alkyl-1-alkynes Synthesis: 3-Ethyl-1-hexyne (58, 1)
β-Hydroxy Esters from Ethyl Acetate and Aldehydes or Ketones: Ethyl 1-Hydroxycyclohexylacetate (53, 66)
Indoles from Anilines: Ethyl 2-Methylindole-5-carboxylate (56, 72)
Stereoselective Synthesis of Trisubstituted Olefins: Ethyl 4-Methyl-(E)-4,8-nonadienoate (53, 116)
Metalation of 2-Methylpyridine Derivatives: Ethyl 6-Methylpyridine-2-acetate (52, 75)
Ethyl 1-Naphthylacetate (50, 77)
Ethyl (E)-3-Nitroacrylate [Replaced by Methyl (E)-3-Nitroacrylate] (56, 65; replaced)
γ-Ketoesters from Aldehydes via Diethyl Acylsuccinates: Ethyl 4-oxohexanoate (58, 79)
Ethyl Pyrrole-2-Carboxylate (51, 100)
Thiazoles from Ethyl Isocyanoacetate and Thiono Esters: Ethyl Thiazole-4-carboxylate (59, 183)
Carboxylation of Aromatic Compounds: Ferrocenecarboxylic Acid (56, 28)
Fluorinations with Pyridinium Polyhydrogen Fluoride Reagent: 1-Fluoroadamantane (58, 75)
Aldehydes from Aromatic Nitriles: 4-Formylbenzenesulfonamide (51, 20)
Geranyl Chloride (54, 63)
Allylic Chlorides from Allylic Alcohols: Geranyl Chloride (54, 68)
Glutaconaldehyde Sodium Salt From Hydrolysis of Pyridinium-1-sulfonate (59, 79)
Aldehydes from Primary Alcohols by Oxidation with Chromium Trioxide: Heptanal (52, 5)
Conversion of Nitro to Carbonyl by Ozonolysis of Nitronates: 2,5-Heptanedione (56, 36)
Macrocyclic Polyamines: 1,4,7,10,13,16-Hexaäzacycloöctadecane (58, 86)
Cuprous Ion-Catalyzed Oxidative Cleavage of Aromatic o-Diamines by Oxygen:(Z,Z)-2,4-Hexadienedinitrile (57, 33)
Hexafluoroacetone Imine (50, 81)
3-Trimethylsilyl-3-buten-2-one as Michael Acceptor for Conjugate Addition-Annelation: cis-4,4a,5,6,7,8-Hexahydro-4a,5-dimethyl-2(3H)-naphthalenone (58, 158)
Nitrones for Intramolecular 1,3-Dipolar Cycloadditions: Hexahydro-1,3,3,6-tetramethyl-2,1-benzisoxazoline (58, 106)
(E)-4-Hexen-1-ol (55, 62)
Fragmentation of α,β-Epoxyketones to Acetylenic Aldehydes and Ketones: Preparation of 2,3-Epoxycyclohexanone and its Fragmentation to 5-Hexynal (55, 52)
γ-Hydroxy-α,β-Unsaturated Aldehydes via 1,3-Bis(methylthio)allyllithium: trans-4-Hydroxy-2-hexenal (54, 19)
17β-Hydroxy-5-oxo-3,5-seco-4-norandrostane-3-carboxylic Acid (55, 67)
Directed Aldol Condensations: threo-4-Hydroxy-3-phenyl-2-heptanone (54, 49)
Macrolides from Cyclization of ω-Bromocarboxylic Acids: 11-Hydroxyundecanoic Lactone (58, 98)
Direct Iodination of Polyalkylbenzenes: Iododurene (51, 94)
trans-Iodopropenylation of Alkyl Halides: (E)-1-Iodo-4-phenyl-2-butene (56, 77)
2-Iodo-p-xylene (55, 70)
cis-α,β-Unsaturated Acids: Isocrotonic Acid (53, 123)
Trichloromethyl Chloroformate as a Phosgene Equivalent: 3-Isocyanatopropanoyl Chloride (59, 195)
Hydroboration of Olefins: (+)-Isopinocampheol [Replaced by ()-Isopinocampheol] (52, 59)
()-Isopinocampheol (New)
Reaction of Aryl Halides with π-Allylnickel Halides: Methallylbenzene (52, 115)
Sulfonyl Cyanides: Methanesulfonyl Cyanide (57, 88)
1,6-Methano[10]annulene (54, 11)
Vinyl Sulfides from Thioacetals with Copper(I) Trifluoromethanesulfonate: (Z)-2-Methoxy-1-phenylthio-1,3-butadiene (59, 202)
6-Methoxy-β-tetralone (51, 109)
Methyl Groups by Reduction of Aromatic Carboxylic Acids with Trichlorosilane-tri-n-propylamine: 2-Methylbiphenyl (56, 83)
1-d-Aldehydes from Organometallic Reagents: 2-Methylbutanal-1-d (51, 31)
Preparation of Vinyl Trifluoromethanesulfonates: 3-methyl-2-buten-2-yl Triflate (54, 79)
Preparation and Reductive Cleavage of Enol Phosphates: 5-Methylcoprost-3-Ene (52, 109)
Oxymercuration-Reduction: Alcohols from Olefins: 1-Methylcyclohexanol (53, 94)
Reductive Cleavage of Allylic Alcohols, Ethers, or Acetates to Olefins: 3-Methylcyclohexene (56, 101)
γ-Ketoesters to Prepare Cyclic Diketones: 2-Methyl-1,3-cyclopentanedione (58, 83)
Sulfide Contraction via Alkylative Coupling: 3-Methyl-2,4-Heptanedione (55, 127)
Isoxazole Annelation Reaction: 1-Methyl-4,4a,5,6,7,8-Hexahydronaphthalen-2(3H)-one (53, 70)
Addition of Organolithium Reagents to Allyl Alcohol: 2-Methyl-1-Hexanol (55, 1)
Conversion of Primary Alcohols to Urethanes via the Inner Salt of Methyl (carboxysulfamoyl)Triethylammonium Hydroxide: Methyl n-Hexylcarbamate (56, 40)
Methyl 2-Alkynoates from 3-Alkyl-2-pyrazolin-5-ones: Methyl 2-Hexynoate (55, 73)
Methyl (trans-2-Iodo-1-Tetralin)carbamate (51, 112)
Methyl Nitroacetate (55, 77)
Methyl (E)-3-Nitroacrylate (New)
2-Methyl-2-nitrosopropane and Its Dimer (52, 77)
Nucleophilic Acylation with Disodium Tetracarbonylferrate: Methyl 7-Oxoheptanoate and Methyl 7-Oxoöctanoate (59, 102)
Aldehydes from Allylic Alcohols and Phenylpalladium Acetate: 2-Methyl-3-phenylpropionalde (51, 17)
Endocyclic Enamine Synthesis: N-Methyl-2-phenyl-Δ2-tetrahydropyridine (54, 93)
Hydrogenolysis of Carbon-Halogen Bonds with Chromium(II)-en Perchlorate: Naphthalene from 1-Bromonaphthalene (52, 62)
Thiophenols from Phenols: 2-Naphthalenethiol (51, 139)
S(-)-α-(1-Naphthyl)ethylamine (55, 80)
Alkyl Iodides: Neopentyl Iodide and Iodocyclohexane (51, 44)
Sulfide Synthesis in Preparation of Dialkyl and Alkyl Aryl Sulfides: Neopentyl Phenyl Sulfide (58, 143)
4-Nitrobenzyl Fluoride (57, 72)
1-Nitrocycloöctene (50, 84)
Formation and Photochemical Wolff Rearrangement of Cyclic α-Diazo Ketones: D-Norandrost-5-en-3β-ol-16-carboxylic Acids (52, 53)
Highly Reactive Magnesium for the Preparation of Griignard Reagents: 1-Norbornanecarboxylic Acid (59, 85)
Δ9,10-Octalin (50, 88)
2,2,7,7,12,12,17,17-Octamethyl-21,22,23,24-tetraoxaperhydroquaterene (57, 74)
Orcinol Monomethyl Ether (53, 90)
1,6-Oxido[10]annulene (55, 86)
Cyanide-Catalyzed Conjugate Addition of Aryl Aldehydes: 4-Oxo-4-(3-pyridyl)butyronitrile (59, 53)
Aldehydes from sym-Trithlane: n-Pentadecanal (51, 39)
(Pentafluorophenyl)acetonitrile (57, 80)
Pentafluorophenylcopper Tetramer, a Reagent for Synthesis of Fluorinated Aromatic Compounds (59, 122)
trans-3-Penten-2-one (51, 115)
Arene Oxide Synthesis: Phenanthrene-9,10-oxide (58, 12)
Free-Radical Alkylation of Quinones: 2-Phenoxymethyl-1,4-Benzoquinone (56, 68)
3-Phenyl-2H-azirine-2-carboxaldehyde (57, 83)
Phase-Transfer Alkylation of Nitriles: 2-Phenylbutyronitrile (55, 91)
Directed Aldol Condensations: β- Phenylcinnamaldehyde (50, 66)
Aldehydes from 2-Benzyl-4,4,6-Trimethyl-5,6-dihydro-1,3(4H)-oxazine: 1-Phenylcyclopentanecarboxaldehyde (51, 24)
Amines from Mixed Carboxylic-Carbonic Anhydrides: 1-Phenylcyclopentylamine (51, 48)
cis-2-Phenylcyclofropanecarboxylic Acid (50, 94)
Substitution of Aryl Halides with Copper(i) Acetylides: 2-Phenylfuro[3,2-b]pyridine (52, 128)
Ketones and Alcohols from Organoboranes: Phenyl Heptyl Ketone, 1-Hexanol, and 1-Octanol (53, 77)
1-Phenyl-1,4-pentadiyne and 1-Phenyl-1,3-pentadiyne (50, 97)
Phenylation with Diphenyliodonium Chloride; 1-Phenyl-2,4-pentanedione (51, 128)
1-Phenyl-4-phosphorinanone (53, 98)
4-Phenyl-1,2,4-triazoline-3,5-dione (51, 121)
2-Phenyl-2-vinylbutyronitrile (55, 99)
Boranes in Functionalization of Olefins to Amines: 3-Pinanamine (58, 32)
Allylic Oxidation with Hydrogen Peroxide-Selenium Dioxide: trans-Pinocarveol (56, 25)
Base-Induced Rearrangement of Epoxides to Allylic Alcohols: trans-Pinocarveol (53, 17)
Polymeric Carbodiimide. Preparation (56, 95)
Alkynes via Phase TransferCatalyzed Dehydrohalogenation: Propiolaldehyde Diethyl Acetal (59, 10)
Rearrangement of Bridgehead Alcohols to Polycyclic Ketones by Fragmentation-Cyclization: 4-Protoadamantanone (Tricyclo[4.3.1.03.8]Decan-4-One) (59, 147)
Quadricyclane (51, 133)
1,2,3,4-Tetrahydro-β-Carboline (51, 136)
Aziridines from β-Iodocarbamates: 1,2,3,4-Tetrahydronaphthalene(1,2)Imine (51, 53)
2,3,4,5-Tetrahydropyridine Trimer (56, 118)
3,3,6,6-Tetramethoxy-1,4-Cyclohexadiene (57, 92)
2,2,3,3-Tetramethyliodocyclopropane (52, 132)
4H-1,4-Thiazine l,1-Dioxide (52, 135)
2-Thiophenethiol (50, 104)
p-Tolylsulfonyldiazomethane (57, 95)
p-Tolylsulfonylmethyl Isocyanide (57, 102)
Tri-tert-Butylcyclopropenyl Tetrafluoroborate (54, 97)
Tricarbonyl[2,3,4,5-η)-2,4,-Cyclohexadien-1-One]Iron and Tricarbonyl[(1,2,3,4,5-η)-2-Methyoxy-2,4-Cyclohexadien-1-Yl]Iron(1+) Hexafluorophosphate(1) from Anisole (57, 107)
Alkylation of Dimedone with a Tricarbonyl(diene)Iron Complex: Tricarbonyl[2-[2,3,4,5-η)-4-Methoxy-2,4-Cyclohexadien-1-yl]-5,5-Dimethyl-1,3-Cyclohexanedione]iron (57, 16)
Cyclobutadiene in Synthesis: endo-Tricyclo[4.4.0.02,5]Deca-3,8-Diene-7,10-Dione (55, 43)
Trifluoroacetylation of Amines and Amino Acids Under Neutral, Mild Conditions: N-Trifluoroacetanilide and N-Trifluoroacetyl-L-Tyrosine (56, 122)
Aldehydes from Acid Chlorides by Modified Rosenmund Reduction: 3,4,5-Trimethoxybenzaldehyde (51, 8)
Oxidation with the Nitrosodisulfonate Radical. I. Preparation and Use of Disodium Nitrosodisulfonate: Trimethyl-p-Benzoquinone (52, 83)
2,2-(Trimethylenedithio)Cyclohexanone (54, 39)
Trimethylene Dithiotosylate and Ethylene Dithiotosylate (54, 33)
Trimethyloxonium Tetrafluoroborate (51, 142)
3,5,5-Trimethyl-2-(2-Oxopropyl)-2-Cyclohexen-1-One (57, 113)
Aldehydes by Oxidation of Terminal Olefins with Chromyl Chloride: 2,4,4-Trimethylpentanal (51, 4)
Trimethylsilyl Azide (50, 107)
3-Trimethylsilyl-3-Buten-2-One: a Michael Acceptor (58, 152)
Tropolone (57, 117)
Preparation of Alkenes by Reaction of Lithium Dipropenylcuprates with Alkyl Halides: (E)-2-Undecene (55, 103; deleted)
General Index
Frmula Index
Hazard Index
Author Index
Concordance Index