✦ LIBER ✦

Generation, nuclear magnetic resonance spectra, and structure of 9-pentacyclo[4.3.0.0.2,4.03,8.05,7]nonyl cations

✍ Scribed by Coates, Robert M.; Fretz, E. Robert

Book ID: 126075549
Publisher: American Chemical Society
Year: 1975
Tongue: English
Weight: 334 KB
Volume: 97
Category: Article
ISSN: 0002-7863
DOI: 10.1021/ja00842a039

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Structure of solid di-9-pentacyclo[4.3.0

Structure of solid di-9-pentacyclo[4.3.0.02,4.03,8.05,7]nonyl ether (“Coates' ether”). Bond shortening in an eclipsed bicyclopropyl

✍ Sushil Srivastava; S. Chang; J. Lauher; G. Jenner; W.J. le Noble 📂 Article 📅 1983 🏛 Elsevier Science 🌐 French ⚖ 145 KB

The X-ray diffraction pattern of the title compound shows the length of the bicyclopropyl bond to be 1.488 + 0.005 i, comparable to the C2C3 bond length of 1,3-butadiene. In our synthesis of Coates' alcohol used in connection with the companion study,

Syntheses of pentacyclo[5.4.0.02,6.03,10

Syntheses of pentacyclo[5.4.0.02,6.03,10.05,9]undecane-4,8,11-trione, pentacyclo[6.3.0.02,6.03,10.05,9]undecane-4,7,11-trione (D3-trishomocubanetrione), and 4,4,7,7,11,11-hexanitropentacyclo[6.3.0.02,6.03,10.05,9]undecane (D3-hexanitrotrishomocubane)

✍ Marchand, Alan P.; Sharma, G. V. Madhava; Annapurna, G. S.; Pednekar, P. R. 📂 Article 📅 1987 🏛 American Chemical Society 🌐 English ⚖ 790 KB

Synthesis of alkene-substituted pentacyc

Synthesis of alkene-substituted pentacyclo[5.4.0.02,6.33,10.05,9]undecanes. 2. Photoelectron spectra and electronic structures of substituted pentacyclo[5.4.0.02,6.03,10.05,9]undecanes

✍ Marchand, Alan P.; Huang, Chunmin; Kaya, Riza; Baker, A. David; Jemmis, Eluvathi 📂 Article 📅 1987 🏛 American Chemical Society 🌐 English ⚖ 1007 KB

Reactivity and degenerate rearrangement

Reactivity and degenerate rearrangement in the solvolysis of pentacyclo[4.3.0.02,4.03,8.05,7]non-9-yl p-nitrobenzoate

✍ Coates, Robert M.; Kirkpatrick, Joel L. 📂 Article 📅 1968 🏛 American Chemical Society 🌐 English ⚖ 365 KB

Remote and proximate substituent effects

Remote and proximate substituent effects on trishomocyclopropenium ion formation in the solvolysis of methyl and phenyl substituted 9-pentacyclo[4.3.0.02,4.03,8.05,7]nonyl p-nitrobenzoates

✍ Coates, Robert M.; Fretz, E. Robert 📂 Article 📅 1977 🏛 American Chemical Society 🌐 English ⚖ 393 KB

Solvolysis of 9-aryl-9-pentacyclo[4.3.0.

Solvolysis of 9-aryl-9-pentacyclo[4.3.0.02,4.03,8.05,7]nonyl p-nitrobenzoates. Unambiguous evidence for the presence of carbon participation by the application of the tool of increasing electron demand

✍ Brown, Herbert C.; Ravindranathan, M. 📂 Article 📅 1977 🏛 American Chemical Society 🌐 English ⚖ 264 KB