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Stereoselective "Pinacol" Coupling of 2,3-O-Isopropylidene-D-glyceraldehyde.
1997
Michael C. Barden, and Jeffrey Schwartz
Department of Chemistry, Princeton University, Princeton, New Jersey 08544-1009.
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Michael C. Barden, and Jeffrey Schwartz
Synthesis of (-)-noviose from 2,3-O-isopropylidene-D-erythronolactol.
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Michael C. Barden, and Jeffrey Schwartz
One-Pot Stereoselective Synthesis of Furantetrahydroquinoline Derivatives Using d/l-Ribose with a 2,3-O-Isopropylidene Group.
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Michael C. Barden, and Jeffrey Schwartz
Enantiodivergent synthesis of D- and L-erythro-sphingosines through Mannich-type reactions of N-benzyl-2,3-O-isopropylidene-D-glyceraldehyde nitrone.
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Michael C. Barden, and Jeffrey Schwartz
Addition of lithiated C-nucleophiles to 2,3-O-isopropylidene-D-erythronolactone: stereoselective formation of a furanose C-disaccharide.
December 2003, The Journal of organic chemistry,
Michael C. Barden, and Jeffrey Schwartz
Synthesis of 2,3:4,6-di-O-isopropylidene-D-allopyranose from D-glucose.
August 2005, Carbohydrate research,
Michael C. Barden, and Jeffrey Schwartz
2,3:4,6-Di-O-isopropylidene-alpha-L-sorbofuranose and 2,3-O-isopropylidene-alpha-L-sorbofuranose.
April 2009, Acta crystallographica. Section C, Crystal structure communications,
Michael C. Barden, and Jeffrey Schwartz
Large scale isolation of 1,2:3,4-di-O-isopropylidene-α-D-glucoseptanose and 2,3:4,5-di-O-isopropylidene-β-D-glucoseptanose.
April 2011, Carbohydrate research,
Michael C. Barden, and Jeffrey Schwartz
O-isopropylidene derivatives of D-allulose (D-psicose) and D-erythro-hexopyranos-2,3-diulose.
August 1968, Canadian journal of biochemistry,
Michael C. Barden, and Jeffrey Schwartz
2,3-O-Isopropylidene-α-d-lyxofuranose, the Monoacetone-d-lyxose of Levene and Tipson.
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Michael C. Barden, and Jeffrey Schwartz
Reaction of 2-deoxy-6-O-[2,3-dideoxy-4,6-O-isopropylidene-2,3- (N-tosylepimino)-alpha-D-mannopyranosyl]-4,5-O-isopropylidene-1,3-di-N- tosylstreptamine with potassium hydrogenfluoride.
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