๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Studies towards diarylheptanoid synthesis. Part 2: Synthesis and ring cleavage reactions of tetrahydro-4H-furo[2,3-b]pyran-2-ones

โœ Scribed by Sidika Polat Cakir; Keith T. Mead; Laura T. Smith

Book ID
104254058
Publisher
Elsevier Science
Year
2003
Tongue
French
Weight
415 KB
Volume
44
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Studies towards diarylheptanoid synthesi
Studies towards diarylheptanoid synthesis. Part 1: Synthesis and ring cleavage reactions of hexahydro-2H,5H-pyrano[2,3-b]pyran-2-ones
โœ Wei Li; Keith T. Mead; Laura T. Smith ๐Ÿ“‚ Article ๐Ÿ“… 2003 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 212 KB

Lewis acid promoted anomeric substitution reactions of a stereoselectively prepared hexahydro-2H,5H-pyrano[2,3b]pyran-2-one derivative was studied as a model for diarylheptanoid synthesis. Aromatic nucleophiles consistently provided the expected thermodynamic C-aryl pyranoside product.

Multicomponent Reactions of Furan-2,3-di
Multicomponent Reactions of Furan-2,3-diones: Synthesis and Characterizations of Furo[3,2-c]pyran-4-ones
โœ ฤฐrfan Koca; ฤฐsmail Yฤฑldฤฑrฤฑm; Ertan ลžahin ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons ๐ŸŒ German โš– 236 KB ๐Ÿ‘ 1 views

## Abstract Furo[3,2โ€__c__]pyranโ€4โ€ones, which possess a naturalโ€product skeleton, are synthesized __via__ a simple, oneโ€pot, threeโ€component reaction of furanโ€2,3โ€diones with dialkyl acetylenedicarboxylates and Ph~3~P.