𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Photochemical synthesis of a tricyclo[3.2.1.03,6]octane

✍ Scribed by Frederick D. Lewis; Ronald A. Ruden


Publisher
Elsevier Science
Year
1971
Tongue
French
Weight
212 KB
Volume
12
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Bicycloannulation: A one-step synthesis
✍ Robert M. Cory; Dominic M.T. Chan πŸ“‚ Article πŸ“… 1975 πŸ› Elsevier Science 🌐 French βš– 171 KB

In recent years, a number of publlcatlons have appeared in which the tncyclo [3.2.1.02s7] octan-6-one system (1) IS utlllzed in synthetic intermediates as a convement precursor of blcycle [3 2.11 octane and blcyclo [2.2.2] octane systems.' All of these lnvestlgatlons have employed the copper-catalyz

Tricyclo[3.1.1.03,6]Heptanes: Synthesis
✍ J. Meinwald; J. Mioduski; Spencer T. Olin πŸ“‚ Article πŸ“… 1974 πŸ› Elsevier Science 🌐 French βš– 165 KB

Na, NH3(1) C2H50H \ (\_ Cl CN Cl CN The efficient synthesis of bicyclot2.2.Olhexenes from cyclobutadieneiron tricarbonyl provides a ready source variety of small ring compounds, efforts in the near future. of starting materials for the preparation of a and we hope to describe other, related syntheti

Catalytic synthesis of 3,3-disubstituted
✍ Marta Catellani; Gian Paolo Chiusoli πŸ“‚ Article πŸ“… 1983 πŸ› Elsevier Science 🌐 French βš– 185 KB

A new cyclopropanation reaction leading to the title compounds is descrsed, based on the use of alkynes as cyclopropanating agents. We recently reported the catalytic formation of norbornanes containing different carbon chains in position 2 and