4-methoxybenzyl 2,2,2-trichloroacetimidate

COc1ccc(COC(CCc2ccc(I)cc2)C(CCO[Si](C)(C)C(C)(C)C)C(=O)OC(C)(C)C)cc1
Reaction #265556
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1ccc(COC(CCc2ccc(-c3ccccc3)cc2)C(CCO[Si](C)(C)C(C)(C)C)C(=O)OC(C)(C)C)cc1
Reaction #396641
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1ccc(COCC2=C[C@@H](CO[Si](C)(C)C(C)(C)C)N(C(=O)OC(C)(C)C)CC2=O)cc1
Reaction #714371
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
COC(=O)[C@H]1C[C@@H](OCc2ccc(OC)cc2)CN1C(=O)OC(C)(C)C
Reaction #819554
title compound
Ausbeute 84.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
CCCCCCCCCCC[C@H](CC(=O)OC)OCc1ccc(OC)cc1
Reaction #1109471
product 32
Ausbeute 82.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_05
CC1(C)COC(=O)[C@H]1O
Reaction #1758578
L-pantolactone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_08
COC(=O)[C@@H](CCC(C)C)[C@H](C)OCc1ccc(OC)cc1
Reaction #1857550
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_02
COc1ccc(COC(CCc2ccc(-c3ccccc3)cc2)C(CCO[Si](C)(C)C(C)(C)C)C(=O)OC(C)(C)C)cc1
Reaction #1885956
title compound
Ausbeute 34.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01
COc1ccc(COC(CCc2ccc(I)cc2)C(CCO[Si](C)(C)C(C)(C)C)C(=O)OC(C)(C)C)cc1
Reaction #1885962
title compound
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01
COc1ccc(COC(CCc2ccc(-c3ccccc3)cc2)C(CCO[Si](C)(C)C(C)(C)C)C(=O)OC(C)(C)C)cc1
Reaction #1906050
title compound
Ausbeute 34.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_10
COc1ccc(COC(CCc2ccc(I)cc2)C(CCO[Si](C)(C)C(C)(C)C)C(=O)OC(C)(C)C)cc1
Reaction #1906055
title compound
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_10
CC1(C)COC(=O)[C@H]1O
Reaction #2006575
L-pantolactone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_05
CCOC(=O)C1CC(OCc2ccc(OC)cc2)CC1CC
Reaction #2056804
ethyl 2-ethyl-4-(4-methoxybenzyloxy)cyclopentanecarboxylate
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
CCOC(=O)C1CC(OCc2ccc(OC)cc2)CC1CC
Reaction #2213964
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
COc1ccc(COC(CCc2ccc(-c3ccccc3)cc2)C(CCO[Si](C)(C)C(C)(C)C)C(=O)OC(C)(C)C)cc1
Reaction #2470097
title compound
Ausbeute 34.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_09
COc1ccc(COC(CCc2ccc(I)cc2)C(CCO[Si](C)(C)C(C)(C)C)C(=O)OC(C)(C)C)cc1
Reaction #2470102
title compound
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_09