Components for a combinatorial library of rigid azabicyclic α-L-fucose mimics: First X-ray crystal structure of a stable monoalkylated triazene formed by hydrogenation of an azide-Reference-Cited by-同舟云学术

Components for a combinatorial library of rigid azabicyclic α-L-fucose mimics: First X-ray crystal structure of a stable monoalkylated triazene formed by hydrogenation of an azide

Published:1999-04 Issue:16 Volume:40 Page:3259-3262
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Smelt Kathryn H.,Harrison Amanda J.,Biggadike Keith,Müller Mathias,Prout Keith,Watkin David J.,Fleet George W.J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference9 articles.

1. Photobromination of carbohydrate derivatives. VI. Functionalization at C6 of 2,3,4-Tri-O-acetyl-1,6-anhydro-β-D-glucopyranose

2. Synthesis of (6R)- and (6S)-D-glucose-6-2H through stereospecific photo-bromination of 1,6-anhydro-.BETA.-D-glucopyranose derivative.

3. Radical-Mediated Brominations at Ring Positions of Carbohydrates

4. A straightforward route to hydantocidin analogues with pyranose ring structure

5. Smelt, KH; Blériot, Y; Biggadike, K; Lynn, S; Lane, AL; Watkin, DJ; Fleet, GWJ preceding publication.

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