indium

Nc1cc(-c2ccc(NC(=O)c3ccco3)c(N)c2)ccc1NC(=O)c1ccco1
Reaction #78027
3,3′-diamino-4,4′-di-2-furoylaminobiphenyl
Ausbeute 23.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Nc1cn(C(c2ccccc2)(c2ccccc2)c2ccccc2)c2ncc(Br)nc12
Reaction #155846
2-bromo-5-trityl-pyrrolo[2,3-b]pyrazin-7-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)C(C)(OCC(C)(N)c1cccc(Br)c1)C(F)(F)F
Reaction #168747
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=CCC(O)c1c(Cl)nc(N)nc1Cl
Reaction #168867
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC1(C)C(=O)NC(=O)N1CCNc1ncc(Br)c(-c2cc3cc(N)ccc3s2)n1
Reaction #212635
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(C)C(=O)NC(=O)N1CCNc1ncc(C(F)(F)F)c(-c2cc3cc(N)ccc3s2)n1
Reaction #243445
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCSCC(C)(O)c1cc2cc(N)c(C(F)(F)F)cc2[nH]1
Reaction #276075
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cl.NCC(NC(=O)Cn1nc(-c2ccc(Cl)cc2)n(C[C@H](O)C(F)(F)F)c1=O)c1cccc(C(F)(F)F)c1
Reaction #307879
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COC(=O)C(C)(OCC(C)(N)c1cccc(Br)c1)C(F)(F)F
Reaction #308900
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CCOC(=O)C(F)(F)C(O)c1cc(Br)ccc1F
Reaction #308952
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Nc1ccccc1S(=O)(=O)N1CC=CC1
Reaction #372727
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
N#Cc1cc(N)ccc1-n1cncn1
Reaction #397385
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Nc1cccc(S(=O)(=O)N2CC=CC2)c1
Reaction #405802
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
C=CCC1(O)CCCC1C(=O)OCc1ccccc1
Reaction #418275
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
C=C1[C@H](CO)C[C@H](O)C[C@H]1O[Si](C)(C)C(C)(C)C
Reaction #475929
titled compound
Ausbeute 68.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
C=CC(C)(C)C(O)c1cc(C(=O)OC)ccc1-c1cc(OC)ccc1F
Reaction #491547
product
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
C=CC(C)(C)C(O)c1cc(C(=O)OC)ccc1-c1cc(OC)ccc1F
Reaction #491564
product
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
Nc1cc(N)cc(Nc2ccc(Br)cc2)c1
Reaction #518560
brown oil
Ausbeute 93.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
C=CCC(O)C(OC)OC
Reaction #540782
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
C=CCC(O)C(OC)OC
Reaction #540783
product
Ausbeute 53.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
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