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http://hub.abes.fr/acs/periodical/jacsat/1970/volume_92/issue_12/101021ja00715a026/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/1952/volume_74/issue_19/101021ja01139a520/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1970/volume_92/issue_22/101021ja00725a068/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1953/volume_18/issue_6/101021jo01134a015/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1982/volume_47/issue_1/101021jo00340a010/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/1967/volume_89/issue_21/101021ja00997a061/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1953/volume_75/issue_13/101021ja01109a058/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1951/volume_73/issue_6/101021ja01150a047/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1949/volume_71/issue_8/101021ja01176a522/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1968/volume_33/issue_11/101021jo01275a020/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1971/volume_36/issue_20/101021jo00819a006/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1968/volume_90/issue_19/101021ja01021a027/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1978/volume_43/issue_12/101021jo00406a020/authorship/2
http://hub.abes.fr/acs/periodical/joceah/1978/volume_43/issue_4/101021jo00398a047/authorship/2
http://hub.abes.fr/acs/periodical/joceah/1981/volume_46/issue_10/101021jo00323a026/authorship/2
http://hub.abes.fr/acs/periodical/joceah/1988/volume_53/issue_20/101021jo00255a032/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1950/volume_72/issue_9/101021ja01165a527/authorship/2
http://hub.abes.fr/acs/periodical/joceah/1981/volume_46/issue_26/101021jo00339a033/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/1970/volume_92/issue_8/101021ja00711a040/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1971/volume_93/issue_3/101021ja00732a020/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1988/volume_110/issue_14/101021ja00222a017/authorship/5
http://hub.abes.fr/acs/periodical/joceah/1971/volume_36/issue_8/101021jo00807a004/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1970/volume_92/issue_26/101021ja00729a011/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1980/volume_102/issue_1/101021ja00521a096/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1978/volume_43/issue_4/101021jo00398a046/authorship/1
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Metalloaldimines. 4. Reaction of lithium aldimines with carbonyl compounds and with activated alkyl halides
Cyclopropanes. XXX. Haller-Bauer cleavage of phenyl cyclopropyl ketones
.alpha. Addition and ortho metalation of phenyl isocyanide
Dimethyleneketene: An Attempted Synthesis
Addition Reactions to Ethyl γ,γ,γ-Trifluorocrotonate
Cyclopropanes. XXV. Cyclopropyl anion
Cyclopropanes. XXVIII. Rearrangement and reactivity of the 1-methyl-2,2-diphenylcyclopropyl radical
Isocyanide reductions. A convenient method for deamination
Chiroptical properties of chiral olefins
Cyclopropanes. XXX. Reductive cleavage of cyclopropane rings
Cyclopropanes. XXIV. Sodium-liquid ammonia reduction of optically active cyclopropyl halides
Cyclopropanes. XXII. Cage disproportionation of optically active 1-methyl-2,2-diphenylcyclopropyl radical
Cyclopropanes. XXIX. Stereochemistry of the 1-methyl-2,2-diphenylcyclopropyl radical in and out of solvent cage
Reduction of α- and β-Ketoesters
Metallo aldimines. II. A versatile synthetic intermediate
A New Synthesis of Diethyl 1,1-Cyclobutanedicarboxylate
Cyclopropane. XXVII. Cyclopropyl anion
Coupling of nonvicinal glycols by low-valent titanium
REDUCTION OF TETRAMETHYLENEKETENE DIMER (DISPIRO[4. 1. 4. 1]DODECANE-6, 12-DIONE)
Alkali metals dissolved in optically active solvents
Metallo aldimines. 3. Coupling of lithium aldimines with aryl, vinyl, and acetylenic halides
Cyclopropanes. XXV. Cleavage of cyclopropane rings by solutions of sodium in liquid ammonia
Isocyanide-metal exchange. The synthesis of masked acylcyanides
A Total Synthesis of Linoleic Acid1
Syntheses and chiroptical properties of 4-substituted 2-adamantylidene derivatives. A new sector rule for chiral 1,3-dienes and .alpha.,.beta.-unsaturated carbonyls
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