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For recent reviews on glycosides synthesis, see: (a) Boons, G.-J. Tetrahedron 1996, 52, 1095; (b) Seeberger, P. H.; Haase, W. Chem. Rev. 2000, 100, 4349.
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For recent examples of undesired removal of acid labile groups in the course of glycosidations, see: (a) Belot, F.; Costachel, C.; Wright, K.; Phalipon, L.; Mulard, L. A. Tetrahedron Lett. 2002, 43, 8215; (b) Jayaprakash, K. N.; Radhakrishnan, K. V.; Fraser-Reid, B. Tetrahedron Lett. 2002, 43, 6953; (c) Plante, O. J.; Palmacci, E. R.; Andrade, R. B.; Seeberger, P. H. J. Am. Chem. Soc. 2001, 123, 9545; (d) Roush, W. R.; Narayan, S. Org. Lett. 1999, 1, 899.
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For recent examples of undesired removal of acid labile groups in the course of glycosidations, see: (a) Belot, F.; Costachel, C.; Wright, K.; Phalipon, L.; Mulard, L. A. Tetrahedron Lett. 2002, 43, 8215; (b) Jayaprakash, K. N.; Radhakrishnan, K. V.; Fraser-Reid, B. Tetrahedron Lett. 2002, 43, 6953; (c) Plante, O. J.; Palmacci, E. R.; Andrade, R. B.; Seeberger, P. H. J. Am. Chem. Soc. 2001, 123, 9545; (d) Roush, W. R.; Narayan, S. Org. Lett. 1999, 1, 899.
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For recent examples of undesired removal of acid labile groups in the course of glycosidations, see: (a) Belot, F.; Costachel, C.; Wright, K.; Phalipon, L.; Mulard, L. A. Tetrahedron Lett. 2002, 43, 8215; (b) Jayaprakash, K. N.; Radhakrishnan, K. V.; Fraser-Reid, B. Tetrahedron Lett. 2002, 43, 6953; (c) Plante, O. J.; Palmacci, E. R.; Andrade, R. B.; Seeberger, P. H. J. Am. Chem. Soc. 2001, 123, 9545; (d) Roush, W. R.; Narayan, S. Org. Lett. 1999, 1, 899.
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For recent examples of glycosidations in the presence of the markedly more stable unsubstituted trityl group, see: (a) Ning, J.; Wang, H.; Yi, Y. Tetrahedron Lett. 2002, 43, 7349; (b) Tanaka, H.; Sakamoto, H.; Sano, A.; Nakamura, S.; Nakajima, M.; Hashimoto, S. Chem. Commun. 1999, 1259. TMSOTf mediated removal of trityl groups can be carried out before or after a glycosidation in a one-pot sequential procedure. For example, see: (c) Du, Y.; Zhang, M.; Kong, F. Org. Lett. 2000, 2, 3797; (d) Yu, B.; Xie, J.; Deng, S.; Deng, S.; Hui, Y. J. Am. Chem. Soc. 1999, 121, 12196.
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For recent examples of glycosidations in the presence of the markedly more stable unsubstituted trityl group, see: (a) Ning, J.; Wang, H.; Yi, Y. Tetrahedron Lett. 2002, 43, 7349; (b) Tanaka, H.; Sakamoto, H.; Sano, A.; Nakamura, S.; Nakajima, M.; Hashimoto, S. Chem. Commun. 1999, 1259. TMSOTf mediated removal of trityl groups can be carried out before or after a glycosidation in a one-pot sequential procedure. For example, see: (c) Du, Y.; Zhang, M.; Kong, F. Org. Lett. 2000, 2, 3797; (d) Yu, B.; Xie, J.; Deng, S.; Deng, S.; Hui, Y. J. Am. Chem. Soc. 1999, 121, 12196.
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For recent examples of glycosidations in the presence of the markedly more stable unsubstituted trityl group, see: (a) Ning, J.; Wang, H.; Yi, Y. Tetrahedron Lett. 2002, 43, 7349; (b) Tanaka, H.; Sakamoto, H.; Sano, A.; Nakamura, S.; Nakajima, M.; Hashimoto, S. Chem. Commun. 1999, 1259. TMSOTf mediated removal of trityl groups can be carried out before or after a glycosidation in a one-pot sequential procedure. For example, see: (c) Du, Y.; Zhang, M.; Kong, F. Org. Lett. 2000, 2, 3797; (d) Yu, B.; Xie, J.; Deng, S.; Deng, S.; Hui, Y. J. Am. Chem. Soc. 1999, 121, 12196.
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For recent examples of glycosidations in the presence of the markedly more stable unsubstituted trityl group, see: (a) Ning, J.; Wang, H.; Yi, Y. Tetrahedron Lett. 2002, 43, 7349; (b) Tanaka, H.; Sakamoto, H.; Sano, A.; Nakamura, S.; Nakajima, M.; Hashimoto, S. Chem. Commun. 1999, 1259. TMSOTf mediated removal of trityl groups can be carried out before or after a glycosidation in a one-pot sequential procedure. For example, see: (c) Du, Y.; Zhang, M.; Kong, F. Org. Lett. 2000, 2, 3797; (d) Yu, B.; Xie, J.; Deng, S.; Deng, S.; Hui, Y. J. Am. Chem. Soc. 1999, 121, 12196.
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For the 'nitrilium effect' on glycosidation stereoselectivity, see: (a) Hashimoto, S.; Honda, T.; Ikegami, S. Chem. Commun. 1989, 685; (b) Schmidt, R. R.; Behrendt, M.; Toepfer, A. Synlett 1990, 694; (c) Ratcliffe, A. J.; Fraser-Reid, B. J. Chem. Soc., Perkin Trans. 1 1990, 747; (d) Sinaÿ, P. Pure Appl. Chem. 1991, 63, 519.
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For the 'nitrilium effect' on glycosidation stereoselectivity, see: (a) Hashimoto, S.; Honda, T.; Ikegami, S. Chem. Commun. 1989, 685; (b) Schmidt, R. R.; Behrendt, M.; Toepfer, A. Synlett 1990, 694; (c) Ratcliffe, A. J.; Fraser-Reid, B. J. Chem. Soc., Perkin Trans. 1 1990, 747; (d) Sinaÿ, P. Pure Appl. Chem. 1991, 63, 519.
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For the 'nitrilium effect' on glycosidation stereoselectivity, see: (a) Hashimoto, S.; Honda, T.; Ikegami, S. Chem. Commun. 1989, 685; (b) Schmidt, R. R.; Behrendt, M.; Toepfer, A. Synlett 1990, 694; (c) Ratcliffe, A. J.; Fraser-Reid, B. J. Chem. Soc., Perkin Trans. 1 1990, 747; (d) Sinaÿ, P. Pure Appl. Chem. 1991, 63, 519.
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For the 'nitrilium effect' on glycosidation stereoselectivity, see: (a) Hashimoto, S.; Honda, T.; Ikegami, S. Chem. Commun. 1989, 685; (b) Schmidt, R. R.; Behrendt, M.; Toepfer, A. Synlett 1990, 694; (c) Ratcliffe, A. J.; Fraser-Reid, B. J. Chem. Soc., Perkin Trans. 1 1990, 747; (d) Sinaÿ, P. Pure Appl. Chem. 1991, 63, 519.
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