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1301640

CC(C)[Si](OCc1cc(C2(O)O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)ccc1Cl)(C(C)C)C(C)C
Reaction #74464
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[Si](OCc1cc(C2O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)ccc1Cl)(C(C)C)C(C)C
Reaction #74465
title compound
DOI: 10.6084/m9.figshare.5104873.v1
OCc1cc(C2O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)ccc1Cl
Reaction #74466
title compound
Ausbeute 98.5%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(C2O[C@@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)cc1CBr
Reaction #74467
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(C(O)c2cc([C@@H]3O[C@H](COCc4ccccc4)[C@@H](OCc4ccccc4)[C@H](OCc4ccccc4)[C@H]3OCc3ccccc3)ccc2Cl)nn1
Reaction #74484
title compound
DOI: 10.6084/m9.figshare.5104873.v1
OCc1cc(C2O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)c(Cl)cc1Cl
Reaction #74504
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)c(CO)cc1C1O[C@H](COCc2ccccc2)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #74508
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[Si](OCc1cc(C2OC(COCc3ccccc3)C(OCc3ccccc3)C(OCc3ccccc3)C2OCc2ccccc2)ccc1Cl)(C(C)C)C(C)C
Reaction #289086
DOI: 10.1039/C8SC04228D
COc1ccc(COCC2OC(c3ccc(Cl)c(CBr)c3)C(OCc3ccc(OC)cc3)C(OCc3ccc(OC)cc3)C2OCc2ccc(OC)cc2)cc1
Reaction #408296
DOI: 10.1039/C8SC04228D
OCc1cc(C2O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)c2c(c1Cl)CCO2
Reaction #663504
product 48
Ausbeute 93.9%DOI: 10.6084/m9.figshare.5104873.v1
Clc1c(CBr)cc(C2O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)c2c1CCO2
Reaction #663505
crude product 49
Ausbeute 212.3%DOI: 10.6084/m9.figshare.5104873.v1
OCc1cc([C@@H]2O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)c2c(c1Cl)OCC2
Reaction #663517
product 66
Ausbeute 95.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1cc([C@@H]2O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)ccc1Cl)c1ccccc1
Reaction #663542
title compound
Ausbeute 91.7%DOI: 10.6084/m9.figshare.5104873.v1
OCc1cc([C@@H]2O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)ccc1Cl
Reaction #663543
title compound 105
Ausbeute 100.5%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc([C@@H]2O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)cc1CBr
Reaction #663544
bromide
Ausbeute 203.6%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(C2OC(COCc3ccccc3)C(OCc3ccccc3)C(OCc3ccccc3)C2OCc2ccccc2)cc1CBr
Reaction #1287752
DOI: 10.1039/C8SC04228D
CCOc1ccc(C(O)c2cc(C3OC(COCc4ccccc4)C(OCc4ccccc4)C(OCc4ccccc4)C3OCc3ccccc3)ccc2Cl)nn1
Reaction #1306886
DOI: 10.1039/C8SC04228D
OCc1cc(C2OC(COCc3ccccc3)C(OCc3ccccc3)C(OCc3ccccc3)C2OCc2ccccc2)ccc1Cl
Reaction #1314115
DOI: 10.1039/C8SC04228D
OCc1cc(C2OC(COCc3ccccc3)C(OCc3ccccc3)C(OCc3ccccc3)C2OCc2ccccc2)ccc1Cl
Reaction #1631156
DOI: 10.1039/C8SC04228D
COc1ccc(COCC2O[C@@H](c3ccc(Cl)c(CBr)c3)[C@@H](OCc3ccc(OC)cc3)[C@@H](OCc3ccc(OC)cc3)[C@@H]2OCc2ccc(OC)cc2)cc1
Reaction #2122579
(2S,3R,4R,5R)-2-(3-(bromomethyl)-4-chlorophenyl)-3,4,5-tris(4-methoxybenzyloxy)-6-((4-methoxybenzyloxy)methyl)tetrahydro-2H-pyran
Ausbeute 79.5%DOI: 10.6084/m9.figshare.5104873.v1
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