propylene oxide

—
Reaction #6434
5.001
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)C[C@H](NC(=O)c1cc([N+](=O)[O-])cc([N+](=O)[O-])c1)C(=O)O
Reaction #49627
3,5-dinitrobenzoyl-(S)-leucine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
—
Reaction #53630
polyoxyalkylene bisphenol A
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cc1oc(=O)oc1COC(=O)C1=C(CSN2C=NSC2)CS[C@@H]2C(NC=O)C(=O)N12
Reaction #62546
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
C=CC(=O)NCC(=O)O
Reaction #65593
N-carboxy methyl acrylamide
Ausbeute 292.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=C1c2ccccc2C(=O)N1Cl
Reaction #75006
N-chlorophthalimide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
O=C1c2ccccc2C(=O)N1Cl
Reaction #75007
N-chlorophthalimide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
CCSC(=O)CC(=O)CBr
Reaction #93796
4-bromo-3-oxothiobutyric acid-S-ethyl ester
Ausbeute 58.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CCN1CCN(C(=O)NC(C(=O)O)c2ccc(O)cc2)C(=O)C1=O
Reaction #95977
α-(4-ethylpiperazin-2,3-dione-1-ylcarbonylamino)-4-hydroxyphenylacetic acid
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CC1CO1
Reaction #96135
propylene oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
COc1ccc2c3ccccc3c3ccc(OC)cc3c2c1
Reaction #158253
material
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1N[C@@H](Cc2ccccc2)CS1
Reaction #171175
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(O)CN1CCC(Oc2cc(N3CCOCC3)ccc2C(=O)Nc2cc(Cl)ccc2C(=O)Nc2ccc(Cl)cn2)CC1
Reaction #175581
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(O)COc1ccc(Oc2cccc(F)c2)cc1
Reaction #176739
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(O)Cc1ccco1
Reaction #178625
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(O)c1ccccc1
Reaction #181621
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(O)Cc1c(Cl)cccc1Br
Reaction #181965
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCc1cccc(CC)c1NCC(C)O
Reaction #188517
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=C(CBr)C(C(=O)OCCCC)N1C(=O)C(NC(=O)COc2ccccc2)C1SN1C(=O)c2ccccc2C1=O
Reaction #198403
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCN1CCN(C(=O)NC(C(=O)O)c2ccc(O)cc2)C(=O)C1=O
Reaction #206233
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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