✦ LIBER ✦

Studies of proton addition to exo and endo-tricyclo[3.2.1.02,4]octane

✍ Scribed by Andrew Burritt; James M. Coxon; Robert G.A.R. Maclagan

Publisher: Elsevier Science
Year: 1995
Tongue: French
Weight: 916 KB
Volume: 51
Category: Article
ISSN: 0040-4020
DOI: 10.1016/0040-4020(95)00717-m

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Spectral properties of exo- and endo-tri

Spectral properties of exo- and endo-tricyclo[3.2.1.02,4]octan-8-ones

✍ Richard E. Pincock; John Haywood-Farmer 📂 Article 📅 1967 🏛 Elsevier Science 🌐 French ⚖ 214 KB

The interaction of formally nonconjugated p-orbital systems has been observed in ultraviolet spectra &.g., changes in n + v\* \* and II + II transition energies and intensities for C=C-C-C=0 structures (2) ) as well as in increased rates of carbonium ion reactions (=.g., solvolysia of homoallylic st

Regiospecific addition of TCNE to 2-exo-

Regiospecific addition of TCNE to 2-exo-methyl-endo-tricyclo [3.2.1.02,4] oct-6-ene

✍ J.M. Coxon; M. de Bruijn; C.K. Lau 📂 Article 📅 1975 🏛 Elsevier Science 🌐 French ⚖ 173 KB

Photoisomerization of endo- and exo-tric

Photoisomerization of endo- and exo-tricyclo[3.2.1.02,4]octene-6

✍ Peter K. Freeman; Donald G. Kuper; V.N. Mallikarjuna Rao 📂 Article 📅 1965 🏛 Elsevier Science 🌐 French ⚖ 136 KB

Syntheses of tetracyclo[3.3.0.0. 2\*804.6]octan-3-one (II) by d,ehydro-

The reactions of exo- and endo-tricyclo[

The reactions of exo- and endo-tricyclo[3,2,12,4]octan-8-ylidenes

✍ Shun-Ichi Murahashi; Kazuo Okumura; Takeji Kubota; Ichiro Moritani 📂 Article 📅 1973 🏛 Elsevier Science 🌐 French ⚖ 187 KB

Die Cyclopropylcarbinyl-Cyclobutyl-Homoa

Die Cyclopropylcarbinyl-Cyclobutyl-Homoallyl-Umlagerung. I. Teil. Synthese von Tricyclo[3.2.1.02,7]octan-3-ol, endo- und exo-Tricyclo[3.2.1.03,6]octan-4-ol und exo-Bicyclo[3.2.1]-oct-2-en-7-ol

✍ Manfred Geisel; Cyril A. Grob; Werner Santi; Werner Tschudi 📂 Article 📅 1973 🏛 John Wiley and Sons 🌐 German ⚖ 737 KB

## Abstract Tricyclo[3.2.1.0^2,7^]octan‐3‐ol (**1**) and its 4‐isomer **7** were obtained by hydroboration of tricyclo[3.2.1.0^2,7^]oct‐3‐ene (**5**). The former alcohol **1** is quantitatively converted to the isomeric alcohol __exo__‐bicyclo[3.2.1]oct‐2‐en‐7‐ol (**3**) by treatment with aqueous a

Stereoselective addition of singlet oxyg

Stereoselective addition of singlet oxygen to 8-isopropylidene-tricyclo[3.2.1.02,4]octane derivatives

✍ Keiji Okada; Toshio Mukai 📂 Article 📅 1979 🏛 Elsevier Science 🌐 French ⚖ 213 KB

Sunnnary: Singlet oxygen adds stereoselectively to 8-isopropylidenetricyclo[3.2.1.02y4]octane. The T-orbital distortion and the secondary orbital interaction are discussed in order to explain the observed stereoselectivity. Recently it has been reported by two groups 2,3 that singlet oxygen adds ste