𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The reaction of bicyclo[2.2.1]Heptadiene with amylsodium a novel cleavage reaction

✍ Scribed by R.A. Finnegan; R.S. McNees


Publisher
Elsevier Science
Year
1962
Tongue
French
Weight
126 KB
Volume
3
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


WHEN a pentane suspension of amylsodium was allowed to react for 5 hr at room temperature with an equimolar amount of bicyclo[2.2.l]heptadiene (I) and the reaction mixture forced onto an excess of solid C02, a crystalline acid (II) could be isolated in good yield. This acid KBr , AEtoH max 222 mp, "max 1675 cm-l (a, B -unsaturated acid), provided microanalytical data in close agreement with those calculated for the empirical formula C6H602 while its high melting point (204-205', sublimes) (sealed capillary, corrected) suggested that it was at least dibasic, C H 0 .

12 12 4


📜 SIMILAR VOLUMES


The Reaction of Difluorocarbene with Bic
✍ Charles W. Jefford; Arlette Delay; Timothy W. Wallace; Ulrich Burger 📂 Article 📅 1976 🏛 John Wiley and Sons 🌐 German ⚖ 466 KB

## Abstract The addition of difluorocarbene to bicyclo[2.2.2]octa‐2,5‐diene gave the __exo__ and __endo__ 1:1 cyclopropane adducts. In contrast to norbornadiene, no __homo__‐1,4 adduct was formed. The adducts were thermally stable under the conditions of their formation and separation (<170°). Howe

Reactions of a novel benzyne annelated w
✍ Akira Matsuura; Tohru Nishinaga; Koichi Komatsu 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 280 KB

Anthmnilic acid 9 amI odibromobenzme 14 annelated with two bicyclo[2.2.2]octene units were synthesized as the precursors for titled benzyne 3. The generation of 3 was confkmed by trapping with forao and its derivative. In the absence of trapping agent, benzyne 3 generated by diamtization of 9 gave a

A novel CC bond cleavage reaction of 2,
✍ Rui Ren; Pin Yang; Xiang-Lin Jin 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 195 KB

## Abstract 2,2′‐Pyridil reacted with CuCl~2~ to give C–‐C bond cleavage product (picolinate)~2~Cu, and its structure has been unambiguously confirmed by an X‐ray structural analysis.

The Reaction of Bicyclo [3.2.1] octenyl
✍ C. W. Jefford; A. Sweeney; F. Delay 📂 Article 📅 1972 🏛 John Wiley and Sons 🌐 German ⚖ 897 KB

## Abstract Reduction of 2‐phenyl‐ and 2‐methyl‐__exo__‐3,4‐dichlorobicyclo[3.2.1]oct‐2‐enes with lithium aluminium hydride (LAH) or tributyltin hydride (TBTH) gave __endo__‐2‐phenyl‐3‐chlorobicyclo[3.2.1]oct‐3‐ene, 2‐phenyl‐3‐chlorobicyclo[3.2.1]oct‐2‐ene and their methyl analogues. The action of