𝔖 Bobbio Scriptorium
✦   LIBER   ✦

2:1 Adduct from diphenylketene and 1,1-diphenylethylene. 3,4-Dihydro-1,4,4-triphenyl-2-naphthyl diphenylacetate

✍ Scribed by Baldwin, John E.; Johnson, Donald S.

Book ID
121470492
Publisher
American Chemical Society
Year
1973
Tongue
English
Weight
660 KB
Volume
38
Category
Article
ISSN
0022-3263

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

2-(1,4-Dioxo-1,4-dihydro-2-naphthyl)-2-m
2-(1,4-Dioxo-1,4-dihydro-2-naphthyl)-2-methylpropanoic acid
✍ Dempster-Rivett, Kieran J. ;Main, Lyndsay ;Nicholson, Brian K. ;Denny, William A πŸ“‚ Article πŸ“… 2007 πŸ› International Union of Crystallography 🌐 English βš– 647 KB

The sterically crowded title compound, C~14~H~12~O~4~, crystallizes as centrosymmetric hydrogen-bonded dimers involving the carboxyl groups. The naphthoquinone ring system is folded by 11.5β€…(1)Β° about a vector joining the 1,4-C atoms, and the quinone O atoms are displaced from the ring plane, presum

Synthesis of substituted 1-benzyl-2,4,6-
Synthesis of substituted 1-benzyl-2,4,6-triphenyl-2,3-dihydro-pyrazolo [3,4-b] [1,4]diazepines
✍ Braulio Insuasty; Ricaurte Rodriguez; Jairo Quiroga; Roberto Martinez; Enrique A πŸ“‚ Article πŸ“… 1997 πŸ› Journal of Heterocyclic Chemistry 🌐 English βš– 210 KB πŸ‘ 1 views

## Abstract The acid catalyzed condensation of 4,5‐diaminopyrazoles and chalcones gave the hitherto unknown 1‐benzyl‐2,4,6‐triphenyl‐2,3‐dihydropyrazolo[3,4‐__b__][1,4]diazepines derivatives. The structure of all products was supported by ir, ^1^H and ^13^C‐nmr and mass spectra.