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http://hub.abes.fr/acs/periodical/jacsat/1957/volume_79/issue_10/101021ja01567a050/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1975/volume_97/issue_9/101021ja00842a048/authorship/4
http://hub.abes.fr/acs/periodical/achre4/1991/volume_24/issue_7/101021ar00007a003/authorship/1
http://hub.abes.fr/acs/periodical/iepra6/1981/volume_20/issue_2/101021i300002a009/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/1960/volume_82/issue_20/101021ja01505a022/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1951/volume_16/issue_9/101021jo50003a017/authorship/3
http://hub.abes.fr/acs/periodical/joceah/1993/volume_58/issue_16/101021jo00068a038/authorship/7
http://hub.abes.fr/acs/periodical/jacsat/1956/volume_78/issue_16/101021ja01597a044/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1961/volume_83/issue_24/101021ja01485a042/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1956/volume_78/issue_16/101021ja01597a046/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/1953/volume_75/issue_20/101021ja01116a044/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1984/volume_49/issue_12/101021jo00186a040/authorship/3
http://hub.abes.fr/acs/periodical/joceah/1993/volume_58/issue_16/101021jo00068a037/authorship/5
http://hub.abes.fr/acs/periodical/joceah/1959/volume_24/issue_9/101021jo01091a607/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1957/volume_79/issue_12/101021ja01569a034/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/1981/volume_103/issue_11/101021ja00401a023/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/1956/volume_78/issue_16/101021ja01597a045/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1953/volume_75/issue_11/101021ja01107a052/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1958/volume_80/issue_13/101021ja01546a055/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1958/volume_80/issue_18/101021ja01551a045/authorship/1
http://hub.abes.fr/springer/periodical/10593/1995/volume_31/issue_8/B907EF281FA56BFAE053120B220A470D/authorship/1
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Isomer distribution ratios of phenols in aromatic hydroxylation with the hydroxyl radical generated from .alpha.-azohydroperoxide in anhydrous organic media. Comparison with Fenton's reagent
Effects of Dimethylsulfonio and Trimethylammonio Groups on the Dissociation of Substituted Phenols
Sulfilimines. Synthetic applications and potential utilizations
Preparation of N-(arylsulfonyl)sulfoximines by oxidation of N-(arylsulfonyl)sulfilimines with sodium hypochlorite in a two-phase system
Relative Reactivities of Organic Halides in Displacement Reactions. III. Reactions of Mercuric Nitrate with Some Bromoketones, Bromoesters and Bromoethers1,2
The Effect of m-Dichloro and m-Dibromo Groups on the Dissociation and Ultraviolet Spectra of p-Dimethylsulfoniophenols
Effect of Substituent on the Reactivity of ι-Substituted Primary Alkyl Halide in the Reaction with Sodium Thiosulfate1,2
The Synthesis of some Fluorine Substituted Antimalarials
Relative Reactivities of Organic Halides in Displacement Reactions. IV. The Rates of Formolysis of Several Secondary Organic Bromides1
Reactivities of Several ι-Substituted Primary Alkyl Bromides with Tertiary Amines1,2
Steric Effects of m-Methyl Groups on the Conjugative Abilities of Thia, Sulfinyl and Sulfonio Functions in p-substituted Phenols1a
Relative Reactivities of Organic Halides in Displacement Reactions. I. Allylic Chlorides
Synthesis of ι-(bromomethyl)bipyridines and related ι-(bromomethyl)pyridinoheteroaromatics: useful functional tools for ligands in host molecules
Quaternary Ammonium Salts of 1,4-Diazabicyclo[2.2.2]octane
A Further Study of the Dissociation and Association of Furoic and Thenoic Acids and of the Rates of Saponification of Their Ethyl Esters
DEUTERIUM-HYDROGEN EXCHANGE REACTIONS OF BRIDGEHEAD α-DEUTERIUM IN BICYCLIC TRISULFIDE
Ligand-coupling reactions of hypervalent species
Relative Reactivities of Organic Halides in Displacement Reactions. II. Reaction of Mercuric Nitrate with Some Normal Chain Alkyl and Aralkyl Bromides1
Reaction of triphenylsulfonium salt with organolithium reagents
Fragmentation reaction of ylides. IV. Reaction of sulfide and carbene
Side arm effects on cation binding, extraction, and transport functions of oligopyridine-functionalized aza-crown ethers
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