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Kinzy W. Affiliations 1 author 1. Share this article Share with email Share with twitter Share with linkedin Share with facebook. Abstract No abstract provided. Full text links Read article at publisher's site DOI : Smart citations by scite. The number of the statements may be higher than the number of citations provided by EuropePMC if one paper cites another multiple times or lower if scite has not yet processed some of the citing articles.
Explore citation contexts and check if this article has been supported or disputed. An orthogonal and reactivity-based one-pot glycosylation strategy for both glycan and nucleoside synthesis: access to TMG-chitotriomycin, lipochitooligosaccharides and capuramycin. Total Synthesis of Natural Disaccharide Sambubiose.
Hoard , Alexei V. Chemistry — A European Journal , 26 36 , Hammelev , Christian M. ChemSusChem , 13 12 , Gold-catalyzed methodologies in carbohydrate syntheses. An extensive review of studies on mycobacterium cell wall polysaccharide-related oligosaccharides — part I: Synthetic studies on arabinofuranosyl oligosaccharides.
Journal of Carbohydrate Chemistry , 38 , Recent Developments in Stereoselective Chemical Glycosylation.
Asian Journal of Organic Chemistry , 8 6 , Bruce Turnbull. Protecting Groups at the Anomeric Position of Carbohydrates. Carbohydrate Research , , Efficient glycosylation with glycosyl ortho-allylbenzoates as donors. Tetrahedron Letters , 60 1 , Organic Chemistry Frontiers , 5 23 , Gold-catalyzed glycosylation in the synthesis of complex carbohydrate-containing natural products. Chemical Society Reviews , 47 21 , European Journal of Organic Chemistry , 19 , Radical halogenation-mediated latent—active glycosylations of allyl glycosides.
Chemical Communications , 54 6 , AuBr 3 -catalyzed azidation of per- O -acetylated and per- O -benzoylated sugars. Beilstein Journal of Organic Chemistry , 14 , Tracking the leaving group in the remote activation of O [ propanyl sulfinyl]benzyl OPSB glycoside. European Journal of Organic Chemistry , 32 , Recent progress on the synthesis of 2-deoxy glycosides.
Science China Chemistry , 60 9 , Practical synthesis of latent disarmed S 2-propylthio benzyl glycosides for interrupted Pummerer reaction mediated glycosylation. Tetrahedron Letters , 58 24 , Gold III chloride.
Asian Journal of Organic Chemistry , 6 2 , An efficient approach to chloro organophosphine gold i complexes for the synthesis of auranofin. Green Chemistry , 19 3 , Shinde , Srinivas Hotha. Expedient synthesis of the heneicosasaccharyl mannose capped arabinomannan of the Mycobacterium tuberculosis cellular envelope by glycosyl carbonate donors.
Chemical Science , 8 3 , Rasmussen , Mikkel H. Marqvorsen , Henrik H. European Journal of Organic Chemistry , 28 , Chemical O-Glycosylations: An Overview. ChemistryOpen , 5 5 , Angewandte Chemie , 27 , Angewandte Chemie International Edition , 55 27 , European Journal of Organic Chemistry , 5 , European Journal of Organic Chemistry , 2 , European Journal of Organic Chemistry , 3 , Glycosylation via remote activation of anomeric leaving groups: development of 2- 2-propylsulfinyl benzyl glycosides as novel glycosyl donors.
Organic Chemistry Frontiers , 3 2 , A versatile glycosylation strategy via Au iii catalyzed activation of thioglycoside donors. Chemical Science , 7 7 , Journal of Synthetic Organic Chemistry, Japan , 74 1 , Homogenous Gold Catalysis.
Angewandte Chemie , 48 , Angewandte Chemie International Edition , 54 48 , European Journal of Organic Chemistry , 18 , Shaikh , Srinivas Hotha.
Transition Metals for the Synthesis of Glycopolymers and Glycopolypeptides. Israel Journal of Chemistry , 55 , When alcohols are used as nucleophiles and strong bases used as catalysts, the result is primarily or exclusively the alpha-galacto-configured adducts. Some studies show that weaker bases may lead to preferential formation of the beta-galacto-configured products instead. The reaction was very successfully extended to other nucleophiles and also to other 2-nitroglycals that undergo base-catalyzed stereoselective Michael-type additions.
Thus, 2-nitroglycals are versatile synthons in glycoconjugate and natural-products synthesis, and it is foreseeable that many more applications will be based on these readily available and highly functionalized skeletons.
Abstract [Reaction: see text]. Publication types Research Support, Non-U. Gov't Review. Substances Glycoconjugates Oligosaccharides Nitrogen.
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