2-aminopropane-1,3-diol

Cc1ccc(C(=O)NC2CC2)cc1-c1ccc(-c2nnc(CNC(CO)CO)o2)cc1
Reaction #59724
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
—
Reaction #64856
product
المردود 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
N#Cc1ccccc1C#N.N#Cc1ccccc1C#N.NC(CO)CO
Reaction #67482
Serinol Bisphthalonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Nc1c(I)c(C(=O)NCC(O)CO)c(I)c(C(=O)NC(CO)CO)c1I
Reaction #70113
5-amino-N1-(1,3-dihydroxypropan-2-yl)-N3-(2,3-dihydroxypropyl)-2,4,6-triiodoisophthalamide
المردود 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)NC(=S)NC(CO)CO
Reaction #76048
1-tert-butyl-3-(2-hydroxy-1-hydroxymethylethyl)thiourea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC1(C)c2cc(C(=O)NC(CO)CO)ccc2C(=O)c2c1[nH]c1cc(C#N)ccc21
Reaction #90041
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)NC(CO)CO)cn1
Reaction #170508
title compound
المردود 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(NC(CO)CO)c1ccc(OCc2conc2-c2ccc(F)cc2)nc1
Reaction #170617
title compound
المردود 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(NC(CO)CO)c1ccc(OCc2conc2-c2ccc(Cl)cc2)nc1
Reaction #170630
title compound
المردود 38.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=S(=O)(NC(CO)CO)c1ccc(Br)s1
Reaction #174454
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCc1noc(C)c1CCc1nc(C)c(C(=O)NC(CO)CO)s1
Reaction #182353
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCC(CO)NC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #205625
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1nc2nc(SCc3ccccc3)nc(NC(CO)CO)c2s1
Reaction #226239
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(C(=O)NC(CO)CO)cc1C=Cc1ccc(Br)cc1
Reaction #228868
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(C(=O)NC(CO)CO)cc1C=Cc1ccc(Br)cc1
Reaction #237598
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(C(=O)NC(CO)CO)cc1C=Cc1ccc(C(F)(F)F)cc1
Reaction #244941
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(F)ccc1-c1nc(NC(CO)CO)nc2c1ccc(=O)n2C1CC1
Reaction #249976
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(F)ccc1-c1nc(NC(CO)CO)nc2c1ccc(=O)n2-c1c(F)cccc1F
Reaction #260536
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1nc(CSc2nc(NC(CO)CO)c3sc(N)nc3n2)cs1
Reaction #267269
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=S(=O)(NC(CO)CO)c1ccc(Cl)s1
Reaction #273298
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
الصفحة 1التالي