𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Photochemical reaction products. CI:8b-methoxy-1,3-diphenyl-2a,8b-dihydrocyclobuta[a]naphthalene. CII:8b-methoxy-2,3-diphenyl-2a,8b-dihydrocyclobuta[a]naphthalene

✍ Scribed by B. J. Poppleton

Book ID
105129717
Publisher
Springer
Year
1980
Tongue
English
Weight
548 KB
Volume
10
Category
Article
ISSN
1572-8854

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Reactions of the dimethyl cyclobutane-1,
Reactions of the dimethyl cyclobutane-1,2-dicarboxylate dianion. A simple synthesis of 1,2-dihydrocyclobuta [b] naphthalene-3, 8-dione
✍ Peter J. Garratt; Robert Zahler 📂 Article 📅 1979 🏛 Elsevier Science 🌐 French ⚖ 148 KB

Vicinal diester dianions have considerable potential as synthetic intermediates, have recently described the formation and basicities of the dimethyl cyclobutane-l,Z-. dicarboxylate dianion (1) and the dimethyl cyclobut-3-ene-1,2-dicarboxylate dianion.\* and we We now report some reactions of dianio

3a,8b-Dihydro-7-methoxy-8b-(trifluoromet
3a,8b-Dihydro-7-methoxy-8b-(trifluoromethyl)-2H-indeno[1,2-b]furan-2,4(3H)-dione
✍ Ukerun, Sylvester Ohwevwo 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 English ⚖ 166 KB

Indeno[ 1, furan-2,4(3H)-dione derivative pentachloride gave an indanone 5, instead of the expected dihydrofuran 6. The mechanism for the formation of the indanone 5 implies the intermediate acid chloride 7. The formation of 5 instead of 6 is due to facilitation of electrophilic attack of the chlor

2a,8a-Di­chloro-2a,8a-di­hydro-1-phenyl­
2a,8a-Di­chloro-2a,8a-di­hydro-1-phenyl­di­chloro­cyclo­buta­[b]­naphthalene-3,8-dione
✍ Shi, Hou-Guang ;Li, Xue-Mei ;Xu, Jian-Hua ;Zhang, Shu-Sheng ;Fun, Hoong-Kun 📂 Article 📅 2003 🏛 International Union of Crystallography 🌐 English ⚖ 230 KB

Single-crystal X-ray study T = 293 K Mean '(C±C) = 0.005 A Ê R factor = 0.047 wR factor = 0.128 Data-to-parameter ratio = 10.4 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.