thioanisole

CSc1ccc(C(C)=O)cc1
Reaction #1160
4-(methylthio)acetophenone
المردود 88.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)[C@@H]1CC[C@H]2CC(NC(=O)OCc3ccccc3)C(=O)N21
Reaction #10520
methyl (3S,7aS)-6-benzyloxycarbonylamino-5-oxohexahydropyrrolizine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#C[C@@H]1CC[C@H]2C[C@@H](N)C(=O)N21.O=C(O)C(F)(F)F
Reaction #10522
(3S,6R,7aS)-6-amino-5-oxohexahydropyrrolizine-3-carbonitrile trifluoroacetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
NCCC[C@H](NC(=O)c1ccc(CNCc2ccccn2)s1)C(=O)O
Reaction #11948
title compound
المردود 53.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1N[C@H]2C/C=C\C[C@@H]1N(c1ccc3ccccc3c1)C2=O
Reaction #68902
Z-(1S,6S)-7-naphthalen-2-yl-7,9-diaza-bicyclo[4.2.2]dec-3-ene-8,10-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
N#Cc1nc2ccc3cc(N)ccc3c2s1
Reaction #92792
product
المردود 94.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)C[C@H](N)C(=O)Nc1ccc2c(ccc3nc(C4=NC(C(=O)O)CS4)sc32)c1
Reaction #92795
2-(7-(Leucinyl)aminonaphtho[2,1-d]thiazol-2-yl)-4,5-dihydrothiazole-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CSCSc1ccccc1
Reaction #94088
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
Nc1ncccc1-c1cc(Cc2ccc(O)cc2)no1
Reaction #164996
title compound
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1ccc(-c2cc(Cc3ccc(O)cc3)no2)c(N)n1
Reaction #165023
title compound
المردود 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1ncc(F)cc1-c1cc(Cc2ccc(O)cc2)no1
Reaction #165366
title compound
المردود 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1ccc(-c2cc(Cc3ccc(O)cc3)no2)cn1
Reaction #165367
title compound
المردود 74.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1ncc(Cl)cc1-c1cc(Cc2ccc(O)cc2)on1
Reaction #165380
title compound
المردود 62.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cn1c(=O)c(-c2ccc(Cl)cc2Cl)cc2c3cc(-c4csc(CN)n4)ccc3n(C)c21
Reaction #175567
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)C(Cc1ccc(O)cc1)NS(=O)(=O)c1ccc(N2CCC(c3ccccc3)CC2)cc1
Reaction #176199
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1ccc(C(=O)NCc2cc3ccc(O)cc3o2)c(N)n1
Reaction #177710
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1ccccc1-c1ccc(NC(=O)C2CC(O[Si](C)(C)C(C)(C)C)CN2C(=O)OC(C)(C)C)c(F)c1
Reaction #190573
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Oc1cc(Br)cc(Nc2cccnc2)c1
Reaction #191125
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1ccccc1-c1ccc(NC(=O)C2CCCN2C(=O)OC(C)(C)C)cc1
Reaction #194300
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C(=CC1CCCC1)c1ccc(SC)cc1
Reaction #195004
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
الصفحة 1التالي