𝔖 Bobbio Scriptorium
✦   LIBER   ✦

An approach to lipophilic nucleotide phosphate analogs: Synthesis of a lipophilic isostere of ATP

✍ Scribed by Renee M. Otoski; Craig S. Wilcox

Book ID
103401127
Publisher
Elsevier Science
Year
1988
Tongue
French
Weight
314 KB
Volume
29
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

A novel approach to the synthesis of lip
A novel approach to the synthesis of lipophilic thymidinemonophosphoglucopyranosides as drug delivery systems
✍ Antonio De Nino; Angelo Liguori; Antonio Procopio; Edoardo Roberti; Giovanni Sin πŸ“‚ Article πŸ“… 1996 πŸ› Elsevier Science 🌐 English βš– 523 KB

The paper describes the synthesis of the hexadecyl phosphotriesters of thymidine 3'-(5'-deoxythymidin-5'-yl phosphate), thymidine 5'-(5'-deoxythymidin-5'-yl phosphate), thymidine 5'-(3',5'-dideoxythymidin-5'-yl phosphate), thymidine 3'-[(methyl 6-deoxy-a-D-glucopyranosid-6-yl) phosphate], and thymid

A convenient procedure for moderate-scal
A convenient procedure for moderate-scale Rothemund synthesis of lipophilic porphyrins: an alternative to the Adler–Longo and Lindsey methodologies
✍ Maxwell J. Crossley; Pall Thordarson; (the late) J. Patrick Bannerman; Philip J. πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 91 KB πŸ‘ 2 views

Rothemund synthesis of porphyrins is conveniently achieved using p-toluenesulfonic acid-catalysed reaction between pyrrole and aldehyde with azeotropic removal of the water formed in the reaction. These conditions are suitable for moderate-scale reactions and involve an easy work-up. In this way, 5,