Zobrazeno 1 - 10
of 86
pro vyhledávání: '"Ferrier carbocyclization"'
Publikováno v:
European Journal of Organic Chemistry. 2020:6645-6648
Autor:
Benjamin M. Swarts, Alex P. Ausmus, Nicholas Banahene, Sarah R. Rundell, Krestina M. Bednarz, Maxwell Hogue, Justin L. Snyder
Publikováno v:
The Journal of Organic Chemistry. 85:3182-3191
Azide-modified inositol (InoAz) analogues are valuable as inhibitors and have shown promise as metabolic chemical reporters (MCRs) for labeling inositol-containing glycoconjugates in eukaryotic cells and potentially in mycobacteria, but the synthesis
Publikováno v:
Tetrahedron. 74:1957-1964
An efficient synthesis of new six-membered carbasugars in both L-form and D-form starting from N–acetylglucosamine is described. The key synthetic steps involved regioselective protection and deprotection, Ferrier carbocyclization, Peterson olefina
Autor:
Arun K. Shaw, Puli Saidhareddy
Publikováno v:
Tetrahedron. 73:6773-6779
A highly stereoselective total synthesis of Amaryllidaceae alkaloid starting from α- d -galactopyranoside has been described. The salient features of this total synthesis are Ferrier carbocyclization reaction for the synthesis of ring A and Suzuki M
Publikováno v:
Synlett. 28:2320-2324
Herein, we report the catalyst-free addition of organozinc species to glycal derivatives and dihydropyrans in a toluene/n-dibutyl ether solvent mixture via a Ferrier rearrangement at room temperature. This methodology requires only a slight excess of
Autor:
Peiran Chen, Jie Su
Publikováno v:
Tetrahedron. 72:84-94
By using Gd(OTf)3 as the catalyst, synthesis of 2,3-unsaturated-glycosides has been performed by Ferrier Rearrangement. A series of 2,3-unsaturated O-, S-, N-, and C-glycosides were obtained from 3,4,6-tri-O-acetyl- d -glucal, 3,4,6-tri-O-benzyl- d -
Akademický článek
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Autor:
Noritaka Chida, Takaaki Sato
Publikováno v:
The Chemical Record. 14:592-605
The Ferrier carbocyclization reaction is one of the most powerful transformations of carbohydrates. This reaction provides enantiomerically pure cyclohexanone derivatives from aldohexoses, and is particularly useful in the chiral pool synthesis of cy
Publikováno v:
IOSR Journal of Applied Chemistry. 7:44-49
A novel procedure for Ferrier rearrangement of tri-O-acetyl-D-glycals in the presence of 3,5- dinitrobenozic acid has been developed. 3,5-Dinitrobenzoic acid is an effective, very cheap and viable catalyst in above synthetic transformations with vari
Publikováno v:
RSC Adv.. 4:34816-34822
An efficient iron-catalyzed decarboxylative C-glycosylation of glycals with β-keto acids via decarboxylative Ferrier rearrangement reaction has been established. This approach provides a wide range of β-keto-functionalized 2,3-unsaturated C-glycosi