✦ LIBER ✦

Base-promoted eliminative cyclization: Novel synthesis of functionalized tetracyclo[6.2.1.02,7.04,10]Undecane and tetracyclo[5.3.0.02,6.05,9]Decane systems

✍ Scribed by Chandler Suri Suresh

Publisher: Elsevier Science
Year: 1990
Tongue: French
Weight: 253 KB
Volume: 31
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)97447-1

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis and flash thermolysis of 1,2,3

Synthesis and flash thermolysis of 1,2,3,4,5,6-hexakis(trifluoromethyl)tetracyclo[4.4.0.02,4.03,5]deca-7,9-diene

✍ Yoshiro Kobayashi; Itsumaro Kumadaki; Akio Ohsawa; Yuji Hanzawa; Masamitsu Honda 📂 Article 📅 1975 🏛 Elsevier Science 🌐 French ⚖ 106 KB

Recently') we reported that the ozonolysis of hexakis(trifluoromethyl)benz-

2,8,10,11-tetrachloro-12-oxahexacyclo-[7

2,8,10,11-tetrachloro-12-oxahexacyclo-[7.2.1.02,8.03,7.04,11.06,10]dodeca-1,9-diol and disorder and mixed crystals in a system of tetracyclo-[6.3.0.04,11.05,9]undecanone and undecanol derivatives

✍ William H. Watson; Ram P. Kashyap; Mariusz Krawiec; Duoli Sun; Thomas F. Carlson 📂 Article 📅 1994 🏛 Springer 🌐 English ⚖ 489 KB

ChemInform Abstract: Tandem 1,3-Dipolar

ChemInform Abstract: Tandem 1,3-Dipolar Cycloaddition of Mesoionic 2,4-Diphenyl-1,3-oxathiolium-5-olate with Cycloocta-1,5-diene. A New Synthesis of the Tetracyclo[6.2.0.04,10.05,9]decane Ring System.

✍ William R. Sponholtz III; Hernando A. Trujillo; Gordon W. Gribble 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 36 KB 👁 1 views

Two fascinating rearrangements through s

Two fascinating rearrangements through selective placement of bromine substituents. Photochemical synthesis of 3-bromo-7-(bromomethyl) tetracyclo[5.3.1.02,6.04,8]undec-10(12)-ene-9,11-dione and its rearrangement with amines

✍ Mangalam S Nair; Uma Sudhir; S Joly; Nigam P Rath 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 426 KB

A novel entry into 3-bromo-7-(bromomethyt)tetracyclo[5.3.1.02"6.04"S]undec~10(12)-ene-9,11-dione, which readily undergoes further rearrangement with primary amines, has been developed through photolysis of 2,5bis(bromomethyl)tricyelo[6.2.1.02"7]undec-4,9-diene-3,6-dione.