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Carbohydrate Research, ISSN 0008-6215, 07/2018, Volume 465, pp. 29 - 34
Synthesis of 1,2-annulated-C-aryl glycosides has been achieved in a stereoselective manner through the Diels-Alder reaction between carbohydrate-derived terminally unsubstituted dienes and in situ generated arynes... 
Annulated sugars | Carbohydrates | Cycloaddition | Sugar-fused (branched) naphthalenes | C-Aryl glycosides | BRADYRHIZOSE | NATURAL-PRODUCTS | BIOCHEMISTRY & MOLECULAR BIOLOGY | ARYLATION | CHEMISTRY, ORGANIC | FUNCTIONALIZATION | NAPHTHOQUINONES | D-GALACTOSE | BERGENIN | INHIBITORS | CHEMISTRY, APPLIED | DERIVATIVES | HYBRIDS | Diels-Alder reaction | Chemical properties
Journal Article
Organic Letters, ISSN 1523-7060, 08/2009, Volume 11, Issue 16, pp. 3734 - 3737
Journal Article
Carbohydrate Research, ISSN 0008-6215, 10/2018, Volume 468, pp. 64 - 68
2-Deoxy-β-C-aryl/alkyl glycosides were synthesized from di-O-pivaloyl protected homoallylic alcohol derived from D-mannitol with various aldehydes via the Prins cyclization... 
Carbohydrates | Glycosylation | C-Aryl/alkyl glycosides | Prins reaction | D-mannitol | NATURAL-PRODUCTS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHEMISTRY, ORGANIC | GLYCALS | ARYLBORONIC ACIDS | METHYL-ESTER | REPEATING UNIT | REGIOSELECTIVE SYNTHESIS | CHEMICAL-SYNTHESIS | CHEMISTRY, APPLIED | ANOMERIC NUCLEOPHILES | STEREOCONTROLLED SYNTHESIS
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 11/2010, Volume 132, Issue 44, pp. 15528 - 15530
Journal Article
Chemical Science, ISSN 2041-6520, 2019, Volume 10, Issue 13, pp. 3840 - 3845
An intramolecular benzyne-diene [4 + 2] cycloaddition with broad substrate scope has been realized by using a cleavable silicon tether, allowing access to... 
ORGANIC-SYNTHESIS | DIVERSITY-ORIENTED SYNTHESIS | CARBON | DIELS-ALDER REACTION | STEREOCHEMISTRY | C-ARYL GLYCOSIDES | FURAN CYCLOADDITIONS | BENZOBARRELENE | ARYNES | CHEMISTRY, MULTIDISCIPLINARY | CYCLIC OLEFINS
Journal Article
Synlett, ISSN 0936-5214, 09/2017, Volume 28, Issue 14, pp. 1719 - 1723
Abstract A facile synthetic method of 2-substituted 3-methoxycarbonyl-4-methoxyfurans has been developed, allowing construction of highly functionalized... 
cluster | natural products | benzyne | cycloaddition | furans | KETENE SILYL ACETAL | BENZOCYCLOBUTENONES | FORMAL SYNTHESIS | ALPHA-ALKOXYBENZYNE | CHEMISTRY, ORGANIC | LACTONAMYCIN | DEOXYGENATION | C-ARYL GLYCOSIDES | DERIVATIVES | EFFICIENT
Journal Article
Beilstein Journal of Organic Chemistry, ISSN 1860-5397, 05/2012, Volume 8, Issue 1, pp. 675 - 682
.... This Pd-catalyzed cross-coupling reaction presents a facile access to alkynyl C-glycosides and sets the stage for a reductive/oxidative refunctionalization of the enyne moiety to regenerate either C... 
Reductive/oxidative refunctionalization | Sonogashira-Hagihara reaction | Glycals | C-glycosides | Enyne | GLYCOSIDES | OLIGOSACCHARIDES | enyne | C-ARYL GLUCALS | CHEMISTRY, ORGANIC | reductive/oxidative refunctionalization | EPOXIDATION | CATALYZED COUPLING REACTION | CONSTRUCTION | ORGANIC HALIDES | DIMETHYLDIOXIRANE | glycals | ACCESS | ISOCHROMANS | Sonogashira–Hagihara reaction
Journal Article
Current Organic Chemistry, ISSN 1385-2728, 04/2005, Volume 9, Issue 6, pp. 503 - 519
Transition-metal-catalyzed or -mediated intramolecular [2 + 2 + 2] alkyne cyclotrimerizations are one of the most efficient method to construct highly... 
BENZENE-DERIVATIVES | CATALYZED 2+2+2 COCYCLIZATION | ONE-STEP SYNTHESIS | POLYCYCLIC AROMATIC-HYDROCARBONS | AMINO-ACIDS | METALATIVE REPPE REACTION | C-ARYL GLYCOSIDES | CHEMISTRY, ORGANIC | DIMETHYL ACETYLENEDICARBOXYLATE | BIS(ALPHA-AMINO ACID) DERIVATIVES | DIYNE REACTION
Journal Article
Synthesis, ISSN 0039-7881, 12/2016, Volume 48, Issue 24, pp. 4555 - 4563
Abstract Two strategies for the synthesis of the gilvocarcins were explored in order to construct the C -arylglycosidic tricyclic core of these natural... 
paper | C-glycosidation | gilvocarcins | Diels-Alder | quinones | decarboxylation | PALLADIUM | ROUTE | ARYLATION | CHEMISTRY, ORGANIC | GLYCALS | CLOSING METATHESIS | ARYLGLYCOSIDES | SUGAR | C-ARYL GLYCOSIDES | RING OXOCARBENIUM IONS | DERIVATIVES
Journal Article
Journal of Carbohydrate Chemistry, ISSN 0732-8303, 10/2012, Volume 31, Issue 8, pp. 603 - 619
Along with the O- and C-aryl glycosides, N-aryl glycosides represent an important class of carbohydrate and heterocyclic aryl conjugates that possess diverse applications and implications of biological interest... 
Click chemistry | O-aryl glycosides | N-aryl glycosides | C-aryl glycosides | OLIGOSACCHARIDES | ACETYL DERIVATIVES | BIOCHEMISTRY & MOLECULAR BIOLOGY | DRUG DISCOVERY | SOLID-PHASE | CHEMISTRY, ORGANIC | CRYSTAL-STRUCTURES | TERMINAL ALKYNES | AROMATIC-AMINES | D-MANNOSE | CLICK-CHEMISTRY | INHIBITORS | Carbohydrates | glycosides
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 01/2009, Volume 74, Issue 2, pp. 685 - 695
Journal Article
Heterocycles, ISSN 0385-5414, 2015, Volume 90, Issue 2, pp. 1240 - 1253
In connection with the total synthesis of the pluramycin-class antibiotics, we recently found dihydroxyanthrone derivatives to be suitable platforms for the installation of bis-C-glycosides... 
(S)-ESPICUFOLIN | ANTITUMOR ANTIBIOTICS | ORGANIC-SYNTHESIS | ANTHRAPYRAN ANTIBIOTICS | Cyclization Reaction | GAMMA-INDOMYCINONE | CHEMISTRY, ORGANIC | ANTIBIOTIC HEDAMYCIN | Aglycon | ISOKIDAMYCIN | Aromatization | Pluramycin | C-ARYL GLYCOSIDES | Oxidation | KIDAMYCIN | ENANTIOSELECTIVE TOTAL-SYNTHESIS
Journal Article
Organic Chemistry Frontiers, ISSN 2052-4110, 09/2014, Volume 1, Issue 7, pp. 798 - 806
An approach to the regio- and stereo-selective construction of 2-deoxy-C-glycosides via Lewis acid-mediated rearrangement of 2,3-anhydro-1-thiopyranosides is disclosed... 
2,3-ANHYDROSUGARS | MECHANISM | PHENOL | C-ARYL GLYCOSIDES | CHEMISTRY, ORGANIC | GLYCALS | DONORS | GLYCOSIDE BOND SYNTHESIS | STEREOSELECTIVE-SYNTHESIS | SUGAR
Journal Article
Beilstein Journal of Organic Chemistry, ISSN 1860-5397, 06/2017, Volume 13, Issue 1, pp. 1064 - 1070
Journal Article
Synlett, ISSN 0936-5214, 03/2013, Volume 24, Issue 4, pp. 522 - 526
Abstract A d -talose derivative underwent unexpected cyclization during a Mitsunobu reaction. A plausible pathway for the reaction involves an attack of the... 
letter | nucleosides | tetrahydroxy-LCB | cyclization | d -talose | Mitsunobu reaction | DIETHYL AZODICARBOXYLATE | ANALOGS | CHEMISTRY, ORGANIC | D-talose | ALCOHOLS | CYCLOETHERIFICATION | ESTERS | C-ARYL GLYCOSIDES | PHOSPHORIC ACID | STEREOSELECTIVE-SYNTHESIS | STEREOCONTROLLED SYNTHESIS
Journal Article
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