Stereoselective Synthesis of β-glycosyl Esters via 1-Hydroxybenzotriazole Mediated Acylation of Glycosyl Hemiacetals.

Highly stereoselective access to β-glycosyl esters was disclosed, employing 1-hydroxybenzotriazole (HOBt) mediated esterification of glycosyl hemiacetals in the presence of EDCI and 1,4-diazabicyclo[2.2.2]octane (DABCO). Mechanistic studies indicated a dynamic kinetic acylation pathway. In addition, a stereoretentive esterification of glycosyl hemiacetals with tert-butyloxycarbonyl ortho-hexynylbenzoate and DMAP was also reported.

[1]  Liming Zhang,et al.  Directed SN2 Glycosylation Employing an Amide-Functionalized 1-Naphthoate Platform Featuring a Selectivity-Safeguarding Mechanism. , 2023, Journal of the American Chemical Society.

[2]  Weiping Zhou,et al.  A Cu(OTf)2-Catalyzed Glycosylation with Glycosyl ortho-N-Phthalimidoylpropynyl Benzoates as Donors. , 2023, Organic letters.

[3]  A. Fairbanks,et al.  Selective Anomeric Acetylation of Unprotected Sugars with Acetic Anhydride in Water. , 2023, Organic letters.

[4]  Peng Xu,et al.  An Anomeric Base‐Tolerant Ester of 8‐Alkynyl‐1‐Naphthoate for the Gold(I)‐Catalyzed Glycosylation Reaction , 2023, Chinese Journal of Chemistry.

[5]  Dapeng Zhu,et al.  Total Synthesis of Starfish Cyclic Steroid Glycosides. Part 3, Formal Total Synthesis of Luzonicosides A and D , 2023, Chinese Journal of Chemistry.

[6]  K. Morimoto,et al.  Metal-Free Synthesis of Acyl Glycosides and Application to Oligosaccharide Synthesis. , 2022, Organic letters.

[7]  Liming Zhang,et al.  An S N 2-Type Strategy toward 1,2- cis -Furanosides , 2022, CCS Chemistry.

[8]  Biao Yu,et al.  Total Synthesis of Starfish Cyclic Steroid Glycosides. , 2022, Angewandte Chemie.

[9]  S. Ren,et al.  Direct β-Mannosylation of Primary Alcohol Acceptors: Trisaccharide Iteration Assembly of β-1,6-Oligomannosides Corresponding to Kakelokelose. , 2022, Organic letters.

[10]  Peng Wang,et al.  Triflic Imide‐Catalyzed Glycosylation of Disarmed Glycosyl ortho‐Isopropenylphenylacetates and ortho‐Isopropenylbenzyl Thioglycosides , 2021, European Journal of Organic Chemistry.

[11]  Biao Yu,et al.  A Mild Glycosylation Protocol with Glycosyl 1‐Methylimidazole‐2‐carboxylates as Donors , 2021, European Journal of Organic Chemistry.

[12]  N. Jayaraman,et al.  Aglycon reactivity as a guiding principle in latent-active approach to chemical glycosylations. , 2021, Carbohydrate research.

[13]  Yue Fu,et al.  A "Traceless" Directing Group Enables Catalytic SN2 Glycosylation toward 1,2-cis-Glycopyranosides. , 2021, Journal of the American Chemical Society.

[14]  G. He,et al.  Palladium-Catalyzed O - and N -Glycosylation with Glycosyl Chlorides , 2020, CCS Chemistry.

[15]  I. Wilson,et al.  Acyl glucuronide reactivity in perspective. , 2020, Drug discovery today.

[16]  M. Belkadi,et al.  Reversing reactivity: stereoselective desulfurative 1,2-trans-O-glycosylation of anomeric thiosugars with carboxylic acids under copper or cobalt catalysis. , 2020, The Journal of organic chemistry.

[17]  T. Kawabata,et al.  Solvent-Dependent Mechanism and Stereochemistry of Mitsunobu Glycosylation with Unprotected Pyranoses. , 2020, Organic letters.

[18]  Guozhi Xiao,et al.  Glycosyl ortho-(1-phenylvinyl)benzoates versatile glycosyl donors for highly efficient synthesis of both O-glycosides and nucleosides , 2020, Nature Communications.

[19]  Changgui Zhao,et al.  Divergent Synthesis of Dihydropyranone Stereoisomers via N‐Heterocyclic Carbene Catalysis , 2019, Advanced Synthesis & Catalysis.

[20]  Tianyi Yang,et al.  Stereoselective oxidative glycosylation of anomeric nucleophiles with alcohols and carboxylic acids , 2018, Nature Communications.

[21]  C. Hametner,et al.  (2-Benzyloxyphenyl)acetyl (BnPAc): A Participating Relay Protecting Group for Diastereoselective Glycosylation and the Synthesis of 1,2-trans Glycosyl Esters , 2018, Synlett.

[22]  W. Klaffke,et al.  Anomeric modification of carbohydrates using the Mitsunobu reaction , 2018, Beilstein journal of organic chemistry.

[23]  Biao Yu Gold(I)-Catalyzed Glycosylation with Glycosyl o-Alkynylbenzoates as Donors. , 2018, Accounts of chemical research.

[24]  Weiping Tang,et al.  Isoquinoline-1-Carboxylate as a Traceless Leaving Group for Chelation-Assisted Glycosylation under Mild and Neutral Reaction Conditions. , 2017, Angewandte Chemie.

[25]  Weiping Tang,et al.  Chiral Catalyst-Directed Dynamic Kinetic Diastereoselective Acylation of Anomeric Hydroxyl Groups and a Controlled Reduction of the Glycosyl Ester Products. , 2017, Organic letters.

[26]  Changgui Zhao,et al.  N-Heterocyclic Carbene Catalyzed Dynamic Kinetic Resolution of Pyranones. , 2016, Angewandte Chemie.

[27]  Weiping Tang,et al.  Chiral Catalyst-Directed Dynamic Kinetic Diastereoselective Acylation of Lactols for De Novo Synthesis of Carbohydrate. , 2015, Organic letters.

[28]  Chunbao Li,et al.  Stereospecific, High-Yielding, and Green Synthesis of β-Glycosyl Esters. , 2015, Journal of agricultural and food chemistry.

[29]  Biao Yu,et al.  Highly stereoselective β-mannopyranosylation via the 1-α-glycosyloxy-isochromenylium-4-gold(I) intermediates. , 2015, Chemistry.

[30]  Paul J Hergenrother,et al.  Glucose conjugation for the specific targeting and treatment of cancer. , 2013, Chemical science.

[31]  S. Sarkar,et al.  Use of iodine for efficient and chemoselective glycosylation with glycosyl ortho -alkynylbenzoates as donor in presence of thioglycosides , 2013 .

[32]  Yunpeng Liu,et al.  Gold(I)-catalyzed glycosylation with glycosyl ortho-alkynylbenzoates as donors: general scope and application in the synthesis of a cyclic triterpene saponin. , 2010, Chemistry.

[33]  Biao Yu,et al.  An efficient glycosylation protocol with glycosyl ortho-alkynylbenzoates as donors under the catalysis of Ph3PAuOTf , 2008 .

[34]  O. Dangles,et al.  Chemical synthesis of hydroxycinnamic acid glucosides and evaluation of their ability to stabilize natural colors via anthocyanin copigmentation. , 2007, Journal of agricultural and food chemistry.

[35]  John R. Harding,et al.  Efficient synthesis of 1β-O-acyl glucuronides via selective acylation of allyl or benzyl d-glucuronate , 2007 .

[36]  D. Crich,et al.  Stereocontrolled glycoside and glycosyl ester synthesis. neighboring group participation and hydrogenolysis of 3-(2'-benzyloxyphenyl)-3,3-dimethylpropanoates. , 2007, Organic letters.

[37]  Yukako Saito,et al.  A novel tert-butoxycarbonylation reagent: 1-tert-butoxy-2-tert-butoxycarbonyl-1,2-dihydroisoquinoline (BBDI) , 2006 .

[38]  D. Holt,et al.  Effective synthesis of 1beta-acyl glucuronides by selective acylation. , 2005, Organic letters.

[39]  Yutaka Yamamoto,et al.  1-tert-butoxy-2-tert-butoxycarbonyl-1,2-dihydroisoquinoline: a novel and chemoselective tert-butoxycarbonylation reagent. , 2002, Organic letters.

[40]  Basel,et al.  Di-tert-butyl dicarbonate and 4-(dimethylamino)pyridine revisited. Their reactions with amines and alcohols , 2000, The Journal of organic chemistry.

[41]  M. Bols,et al.  Simple Synthesis of beta-D-Glucosyl Esters. , 1993 .