benzyloxy acetyl chloride

O=C(COCc1ccccc1)Oc1cc(Cl)ccc1Oc1ccc(Cl)cc1Cl
Reaction #252946
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(COCc1ccccc1)Nc1ccc(Oc2ccnc3ccsc23)c(F)c1
Reaction #255957
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
NC(=O)c1cccnc1NC(=O)COCc1ccccc1
Reaction #263543
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(COCc1ccccc1)N1CCCN(c2ccc(Cl)cc2Cl)CC1
Reaction #265867
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCC(C)C(CN(CC(=O)NC(CCSC)C(=O)OC)Cc1cccc2ccccc12)NC(=O)COCc1ccccc1
Reaction #270580
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=O)NCCC1CCc2ccc(NC(=O)COCc3ccccc3)c(O)c21
Reaction #271236
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(COCc1ccccc1)N1CCC(O)(c2ccc(Cl)cc2Cl)CC1
Reaction #274695
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CN(C(=O)COCc1ccccc1)c1ccc([N+](=O)[O-])cc1
Reaction #281849
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(COCc1ccccc1)N[C@H]1C[C@@H](n2cnc3c(NCC(c4ccccc4)c4ccccc4)nc(Cl)nc32)[C@H](O)[C@@H]1O
Reaction #303074
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Cc1nc(NC(=O)COCc2ccccc2)sc1-c1cnc(Cl)c(NS(=O)(=O)c2ccccc2)c1
Reaction #339890
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
O=C(O)COCc1ccccc1
Reaction #353896
benzyloxyacetic acid
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CC(=O)NC[C@H]1CN(c2ccc(C3CCN(C(=O)COCc4ccccc4)CC3)cc2)C(=O)O1
Reaction #364971
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CC(=O)NC[C@H]1CN(c2ccc(C3=CCN(C(=O)COC(C)=O)CC3)cc2)C(=O)O1
Reaction #364997
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
COC(=O)C(C)c1ccc2cc(OC(=O)COCc3ccccc3)ccc2c1
Reaction #383679
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCN(CC)C(=O)COCc1ccccc1
Reaction #403236
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(=O)NCCC1CCc2ccc(NC(=O)COCc3ccccc3)c(O)c21
Reaction #427870
title compound
Ausbeute 80.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
COc1ccc(CN2C(=O)[C@@H](OCc3ccccc3)[C@H]2C(C)(C)C)cc1
Reaction #440452
(±)-cis-4-tert-butyl-3-benzyloxy-1-p-methoxybenzyl-azetidinone
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
O=C(COCc1ccccc1)NC(C(=O)O)c1ccccc1
Reaction #442511
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
CC1(c2ccccc2)OC(=O)C(OCc2ccccc2)=C1O
Reaction #456318
4-hydroxy-5-methyl-5-phenyl-3-phenylmethoxy-2-(5H)-furanone
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
COC(=O)[C@@](C)(OC(=O)COCc1ccccc1)c1ccc(-c2ccccc2)cc1
Reaction #456339
methyl (S)-(+)-2-[(1,1'-biphenyl)-4-yl]-2-(2-phenylmethoxyacetoyl)oxypropionate
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
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