Dialkylphosphates as stereodirecting protecting groups in oligosaccharide synthesis.

[1]  A. Demchenko,et al.  Development of an arming participating group for stereoselective glycosylation and chemoselective oligosaccharide synthesis. , 2005, Angewandte Chemie.

[2]  J. Yoshida,et al.  Combinatorial synthesis of an oligosaccharide library by using beta-bromoglycoside-mediated iterative glycosylation of selenoglycosides: rapid expansion of molecular diversity with simple building blocks. , 2005, Chemistry.

[3]  J. Yoshida,et al.  Highly efficient synthesis of oligo-N-acetylglucosamines by iterative glycosylation of di- and tetrachlorophthaloyl-protected thioglucosamines , 2005 .

[4]  H. Overkleeft,et al.  Thioglycosides in sequential glycosylation strategies. , 2005, Chemical Society reviews.

[5]  G. Boons,et al.  A general strategy for stereoselective glycosylations. , 2005, Journal of the American Chemical Society.

[6]  Abhisek Banerjee,et al.  Disarming, non-participating 2-O-protecting groups in manno- and rhamnopyranosylation: scope and limitations of sulfonates, vinylogous esters, phosphates, cyanates, and nitrates , 2005 .

[7]  S. Iyer,et al.  Design and synthesis of dimeric heparinoid mimetics. , 2004, The Journal of organic chemistry.

[8]  Xuefei Huang,et al.  Iterative one-pot synthesis of oligosaccharides. , 2004, Angewandte Chemie.

[9]  H. Kunz,et al.  Biomimetic synthesis of the tumor-associated (2,3)-sialyl-T antigen and its incorporation into glycopeptide antigens from the mucins MUC1 and MUC4. , 2004, Chemistry.

[10]  J. Yoshida,et al.  Iterative glycosylation of 2-deoxy-2-aminothioglycosides and its application to the combinatorial synthesis of linear oligoglucosamines. , 2004, Angewandte Chemie.

[11]  Biao Yu,et al.  Synthesis of the Trisaccharide and Tetrasaccharide Moieties of the Potent Immunoadjuvant QS‐21 , 2004 .

[12]  H. Kunz,et al.  N‐Glycosylamide – Abspaltung der anomeren Schutzgruppe und Einsatz als Glycosyldonoren in der Glycosidsynthese , 2003 .

[13]  H. Kunz,et al.  N-glycosyl amides: removal of the anomeric protecting group and conversion into glycosyl donors. , 2003, Angewandte Chemie.

[14]  Wenhui Zhang,et al.  Synthesis of β-(1→6)-branched β-(1→3) glucohexaose and its analogues containing an α-(1→3) linked bond with antitumor activity , 2003 .

[15]  H. Overkleeft,et al.  Sequential one-pot glycosylations using 1-hydroxyl and 1-thiodonors. , 2003, Organic letters.

[16]  A. Fürstner,et al.  Total synthesis of woodrosin I--part 2: final stages involving RCM and an orthoester rearrangement. , 2003, Chemistry.

[17]  P. Seeberger,et al.  Modular synthesis of heparin oligosaccharides. , 2003, Chemistry.

[18]  H. Amer,et al.  Synthesis of neoglycoproteins containing O-methylated trisaccharides related to excretory/secretory antigens of Toxocara larvae. , 2003, Carbohydrate research.

[19]  K. Hazen,et al.  Comparing n-pentenyl orthoesters and n-pentenyl glycosides as alternative glycosyl donors , 2002 .

[20]  J. Ning,et al.  Pure α-linked products can be obtained in high yields in glycosylation with glucosyl trichloroacetimidate donors with a C2 ester capable of neighboring group participation , 2002 .

[21]  J. Yoshida,et al.  A new, iterative strategy of oligosaccharide synthesis based on highly reactive beta-bromoglycosides derived from selenoglycosides. , 2001, Organic letters.

[22]  M. Oberthür,et al.  Directed and Efficient Syntheses of β(1→4)‐Linked Galacto‐Oligosaccharides , 2001 .

[23]  P. Seeberger,et al.  Oligosaccharide synthesis with glycosyl phosphate and dithiophosphate triesters as glycosylating agents. , 2001, Journal of the American Chemical Society.

[24]  D. Crich,et al.  1-Benzenesulfinyl piperidine/trifluoromethanesulfonic anhydride: a potent combination of shelf-stable reagents for the low-temperature conversion of thioglycosides to glycosyl triflates and for the formation of diverse glycosidic linkages. , 2001, Journal of the American Chemical Society.

[25]  D. Crich,et al.  1-ベンゼンスルフィニルピペリジン/トリフルオロメタンスルホン酸無水物 チオグリコシドのグリコシルトリフラートへの低温変換及び種々の異なるグリコシド結合生成用の貯蔵安定性のある試薬の強力な組合せ | 文献情報 | J-GLOBAL 科学技術総合リンクセンター , 2001 .

[26]  Yuguo Du,et al.  An efficient synthesis of julibrosides related to neosaponin , 2001 .

[27]  C. Wong,et al.  Anomeric reactivity-based one-pot oligosaccharide synthesis: a rapid route to oligosaccharide libraries. , 2000, The Journal of organic chemistry.

[28]  S. Gastaldi,et al.  On the Role of Neighboring Group Participation and Ortho Esters in β-Xylosylation:  13C NMR Observation of a Bridging 2-Phenyl-1,3-dioxalenium Ion. , 1999, The Journal of organic chemistry.

[29]  W. Cai,et al.  Chemistry of 4,6-O-Benzylidene-D-glycopyranosyl Triflates: Contrasting Behavior between the Gluco and Manno Series. , 1999, The Journal of organic chemistry.

[30]  Sanxing Sun,et al.  Are Glycosyl Triflates Intermediates in the Sulfoxide Glycosylation Method? A Chemical and 1H, 13C, and 19F NMR Spectroscopic Investigation , 1997 .

[31]  P. Seeberger,et al.  COUPLING OF GLYCAL DERIVED THIOETHYL GLYCOSYL DONORS WITH GLYCAL ACCEPTORS. AN ADVANCE IN THE SCOPE OF THE GLYCAL ASSEMBLY , 1997 .

[32]  Y. Harigaya,et al.  First total synthesis of two new diglycosides, neohancosides A and B, from Cynanchum hancockianum , 1997 .

[33]  J. Tamura,et al.  A stereocontrolled synthetic approach to glycopeptides corresponding to the carbohydrate-protein linkage region of cell-surface proteoglycans. , 1995, Bioorganic & medicinal chemistry.

[34]  A. Varki,et al.  Biological roles of oligosaccharides: all of the theories are correct , 1993, Glycobiology.

[35]  J. Banoub,et al.  Synthesis of oligosaccharides of 2-amino-2-deoxy sugars , 1992 .

[36]  P. Konradsson,et al.  Iodonium promoted reactions of disarmed thioglycosides , 1990 .

[37]  J. H. Boom,et al.  Iodonium ion promoted reactions at the anomeric centre. II An efficient thioglycoside mediated approach toward the formation of 1,2-trans linked glycosides and glycosidic esters , 1990 .

[38]  P. Konradsson,et al.  Armed and disarmed n-pentenyl glycosides in saccharide couplings leading to oligosaccharides , 1988 .

[39]  H. Kunz,et al.  Stereoselektive Glycosylierung von Steroidalkoholen mit 2,3,4,6‐Tetra‐O‐privaloyl‐α‐D‐glucopyranosylbromid (Pivalobromglucose) und 2,3,4,6‐Tetra‐O‐(o‐toluoyl)‐α‐D‐glucopyranosylbromid , 1986 .

[40]  M. Matsui,et al.  Regio- and stereo-controlled synthesis of core oligosaccharides of glycopeptides , 1978 .

[41]  D. B. Denney,et al.  Synthesis and reactions of some tetraalkoxyphosphonium salts , 1969 .