2003
DOI: 10.1016/s0008-6215(03)00337-9
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1,2-O-Trichloroethylidene acetal group protected 3,5-dieno-1,4-furanose derivatives

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Cited by 9 publications
(5 citation statements)
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“…The hydroxyl and carboxylic acid group protons appeared as singlets at 5.48, 5.55, 5.76 ppm and 12.32, 12.42, 12.50 ppm, respectively. The large coupling constants (15.6 to 16.0 Hz) between 5-H and 6-H prove the formation of the E -isomer [ 33 ].…”
Section: Resultsmentioning
confidence: 99%
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“…The hydroxyl and carboxylic acid group protons appeared as singlets at 5.48, 5.55, 5.76 ppm and 12.32, 12.42, 12.50 ppm, respectively. The large coupling constants (15.6 to 16.0 Hz) between 5-H and 6-H prove the formation of the E -isomer [ 33 ].…”
Section: Resultsmentioning
confidence: 99%
“…A two pot alternative synthesis of similar compounds has been reported previously [ 27 , 31 , 33 ]. Hence, now we report synthesis of α,β -unsaturated furanuronic acid derivatives via a more facile one pot procedure using the Knoevenagel-Doebner reaction approach.…”
Section: Resultsmentioning
confidence: 99%
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“…All chemical reagents used in the experiments were of analytical reagent grade, used without further purification, and were purchased from Merck. The synthesis procedure and structural formation of MOADDTCEXHEFU, which is an unsaturated sugar derivative, were reported elsewhere . To use an insoluble form of this material for the adsorption process, this unsaturated molecule was methylated. , This material was stored in a refrigerator.…”
Section: Methodsmentioning
confidence: 99%
“…The synthesis procedure and structural formation of MOADDTCEXHEFU, which is an unsaturated sugar derivative, were reported elsewhere. 9 To use an insoluble form of this material for the adsorption process, this unsaturated molecule was methylated. 10,11 This material was stored in a refrigerator.…”
Section: ' Materials and Experimental Sectionmentioning
confidence: 99%