Regioselective acetolytic de-O-benzylation of poly-O-benzylated sugars can be triggered by the activation of isopropenyl acetate (IPA) with either an iodine/silane combined reagent or iodine alone. Unlike other known acetolysis procedures, the protocols presented here do not suffer from the useofharshacidicreagentsandexcessamountsofhigh-boiling acetic anhydride. The activation of IPA with iodine and triethylsilane (or the cheaper polymethylhydrosiloxane, PMHS)usuallyresultsinshorterreactiontimes,withtheacetolysis occurringpreferentially (with some exceptions)at primary benzyloxy groups. With anomerically armed sugars, anomeric iodination can be a concomitant process to give highly reactive intermediates which can be converted in situ into workable and useful building blocks upon suitable quenchingconditions.Ontheotherhand,IPAactivationwith iodine alone allows the reactions to occur under milder conditions,albeitoverlongertimes.Inalmostallreported examples, IPA can be used in moderate excess (5equiv.), but its employment as the solvent is crucial with an amino sugar model compound otherwise recalcitrant to any acetolytic modification. An additional advantage of these conditions lies in the unprecedented possibility of incorporating the acetolysis step into one-pot synthetic sequences leading to multiple functional modifications of saccharidic substrates. As to the regioselectivity, most reactions seem to be controlled bysteric factors, asthe most accessibleprimary benzyloxy groups are commonly acetolyzed. However, a couple of disclosed examples display that under suitable structural conditions,strainreliefeffectsmightbearulingfactorforthe regiocontrol of the processes. Overall, the reported protocols offer complementary options for experimentally easy access to a wide range of useful saccharide building blocks featuring a varied profile of protecting groups.

Regioselective Acetolysis of Highly O-Benzylated Carbohydrates Promoted by Iodine or an Iodine/Silane Combined Reagent: Use of Isopropenyl Acetate as an Alternative to Acetic Anhydride / M., Giordano; Iadonisi, Alfonso; Pastore, Antonello. - In: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY. - ISSN 1099-0690. - (2013), pp. 3137-3147. [10.1002/ejoc.201300064]

Regioselective Acetolysis of Highly O-Benzylated Carbohydrates Promoted by Iodine or an Iodine/Silane Combined Reagent: Use of Isopropenyl Acetate as an Alternative to Acetic Anhydride

IADONISI, ALFONSO;PASTORE, ANTONELLO
2013

Abstract

Regioselective acetolytic de-O-benzylation of poly-O-benzylated sugars can be triggered by the activation of isopropenyl acetate (IPA) with either an iodine/silane combined reagent or iodine alone. Unlike other known acetolysis procedures, the protocols presented here do not suffer from the useofharshacidicreagentsandexcessamountsofhigh-boiling acetic anhydride. The activation of IPA with iodine and triethylsilane (or the cheaper polymethylhydrosiloxane, PMHS)usuallyresultsinshorterreactiontimes,withtheacetolysis occurringpreferentially (with some exceptions)at primary benzyloxy groups. With anomerically armed sugars, anomeric iodination can be a concomitant process to give highly reactive intermediates which can be converted in situ into workable and useful building blocks upon suitable quenchingconditions.Ontheotherhand,IPAactivationwith iodine alone allows the reactions to occur under milder conditions,albeitoverlongertimes.Inalmostallreported examples, IPA can be used in moderate excess (5equiv.), but its employment as the solvent is crucial with an amino sugar model compound otherwise recalcitrant to any acetolytic modification. An additional advantage of these conditions lies in the unprecedented possibility of incorporating the acetolysis step into one-pot synthetic sequences leading to multiple functional modifications of saccharidic substrates. As to the regioselectivity, most reactions seem to be controlled bysteric factors, asthe most accessibleprimary benzyloxy groups are commonly acetolyzed. However, a couple of disclosed examples display that under suitable structural conditions,strainreliefeffectsmightbearulingfactorforthe regiocontrol of the processes. Overall, the reported protocols offer complementary options for experimentally easy access to a wide range of useful saccharide building blocks featuring a varied profile of protecting groups.
2013
Regioselective Acetolysis of Highly O-Benzylated Carbohydrates Promoted by Iodine or an Iodine/Silane Combined Reagent: Use of Isopropenyl Acetate as an Alternative to Acetic Anhydride / M., Giordano; Iadonisi, Alfonso; Pastore, Antonello. - In: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY. - ISSN 1099-0690. - (2013), pp. 3137-3147. [10.1002/ejoc.201300064]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/572821
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