✦ LIBER ✦

EVIDENCE FOR CYCLOPENTYNE AS A REACTION INTERMEDIATE IN THE COUPLING OF PHENYLLITHIUM WITH 1-CHLOROCYCLOPENTENE 1

✍ Scribed by Roberts, John D.

Book ID: 124167847
Publisher: American Chemical Society
Year: 1960
Tongue: English
Weight: 246 KB
Volume: 82
Category: Article
ISSN: 0002-7863
DOI: 10.1021/ja01502a081

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Evidence for cyclohexyne as an intermedi

Evidence for cyclohexyne as an intermediate in the coupling of phenyllithium with 1-chlorocyclohexene

✍ F. Scardiglia; John D. Roberts 📂 Article 📅 1957 🏛 Elsevier Science 🌐 French ⚖ 143 KB

Evidence of a 1,4-dipole intermediate in

Evidence of a 1,4-dipole intermediate in the reaction of 1-phenyl-4-vinylpyrazole with ptad

✍ Jose Sepulveda-Arques; Mercedes Medio Simón 📂 Article 📅 1985 🏛 Elsevier Science 🌐 French ⚖ 154 KB

Reaction of singlet oxygen with trans-cy

Reaction of singlet oxygen with trans-cyclooctene. Evidence for a 1,2-dioxetane intermediate.

✍ Y. Inoue; N.J. Turro 📂 Article 📅 1980 🏛 Elsevier Science 🌐 French ⚖ 222 KB

Kinetic Evidence for the Triphenylcarbon

Kinetic Evidence for the Triphenylcarbonium Ion as a Reaction Intermediate and Measurement of its Relative Reactivity with Seven Nucleophilic Reagents 1

✍ Swain, C. Gardner; Scott, Carleton B.; Lohmann, Karl H. 📂 Article 📅 1953 🏛 American Chemical Society 🌐 English ⚖ 583 KB

Stereoselective synthesis of 1,2-trans-1

Stereoselective synthesis of 1,2-trans-1-thioglycoses using aluminium chloride: Evidence for 1,2-cis-1-chloroglycopyranosylperacetates as the actual reaction intermediates

✍ B. Rajanikanth; R. Seshadri 📂 Article 📅 1987 🏛 Elsevier Science 🌐 French ⚖ 178 KB

Evidence for a diradical intermediate in

Evidence for a diradical intermediate in the Diels–Alder reaction of 2-butene with cyclohexa-1,3-diene

✍ G. Huybrechts; B. Van Mele 📂 Article 📅 1978 🏛 John Wiley and Sons 🌐 English ⚖ 254 KB

Despite an extensive literature, controversy about the Diels-Alder reaction mechanism still exists. For the thermal dimerization of 1,3-butadiene, for example, a concerted one-step [I] or two-stage [2] mechanism, a mixture of orbital symmetry allowed and forbidden cycloadditions 131, as well as a tw