𝔖 Bobbio Scriptorium
✦   LIBER   ✦

2-(Methoxycarbonyl)-3-phenylprop-2-enyl-3-hydroxynapthalene-2-carboxylate

✍ Scribed by Gayathri, D. ;Velmurugan, D. ;Ravikumar, K. ;Zulykama, Y. ;Perumal, P. T.


Book ID
104490525
Publisher
International Union of Crystallography
Year
2007
Tongue
English
Weight
252 KB
Volume
63
Category
Article
ISSN
1600-5368

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Methyl 2-{[(2E)-3-phenyl­prop-2-enoyl]­a
✍ Vasu, ;Nirmala, K. A. ;Chopra, Deepak ;Mohan, S. ;Saravanan, J. 📂 Article 📅 2004 🏛 International Union of Crystallography 🌐 English ⚖ 308 KB

Single-crystal X-ray study T = 293 K Mean '(C±C) = 0.003 A Ê R factor = 0.045 wR factor = 0.126 Data-to-parameter ratio = 12.3 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.

Penta­fluoro­phenyl 3-phenyl­prop-2-enoa
✍ Andrade, L.C.R. ;Paixão, J. A. ;de Almeida, M.J.M. ;Tavares da Silva, E. J. ;Fer 📂 Article 📅 2005 🏛 International Union of Crystallography 🌐 English ⚖ 131 KB

In the title compound, C 15 H 7 F 5 O 2 , an intramolecular C-HÁ Á ÁO hydrogen bond induces coplanarity of the central chain and the phenyl ring. An intermolecular C-HÁ Á ÁO hydrogen bond leads to the formation of a dimer.

Synthese de methoxycarbonyl-2 methoxy-2
✍ Alfred Saroli; Alain Doutheau 📂 Article 📅 1987 🏛 Elsevier Science 🌐 French ⚖ 217 KB

An oxidative cyclisation of methyl 6-hydroxy P-methoxy 2-hexenoate S and heptenoate 11 leading to title compounds is described. This method has been applied to the synthesis of a methyl glycopyranoside of a methyl heptulosonate.