tetrafluoroborate

CC[Si](CC)(CC)CC
Reaction #48894
tetraethylsilane
المردود 5.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCCCCCCCCCOP(=O)(O)O[C@H](CC(=O)O)C[N+](C)(C)C.[OH-]
Reaction #64412
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
—
Reaction #64421
salt
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
COC(=O)[C@H](CC(C)C)NC(C(=O)N(C)C)c1ccc(F)cc1F
Reaction #73891
methyl N-[1-(2,4-difluorophenyl)-2-(dimethylamino)-2-oxoethyl]-L-leucinate
المردود 58.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)[C@H](CC(C)C)NC(C(=O)N(C)C)c1ccc2occc2c1
Reaction #73901
methyl N-[1-(benzofuran-5-yl)-2-(dimethylamino)-2-oxoethyl]-L-leucinate
المردود 40.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)C(CC(=O)N1CCC(N2Cc3cc(O)ccc3NC2=O)CC1)Cc1cc(Cl)c(N)c(C(F)(F)F)c1
Reaction #173009
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(-c2nocc2C(=O)N2CCC(O)(c3ccccc3Cl)C2)cc1Cl
Reaction #173062
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=N)c1ccc(Cl)cc1F
Reaction #173319
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)n1cc(-c2ccc(C#N)cc2)c2ccc([N+](=O)[O-])cc21
Reaction #173357
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(c1cc(Nc2ccc3c(c2)CC2(C3)C(=O)Nc3ncccc32)ncn1)N1CCc2ccc(F)cc21
Reaction #173402
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(C(=O)NCc2cc3cc(Cl)ccc3[nH]2)ccc1C(=O)N1CCCC1
Reaction #173478
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)c1ccc(CN(CCc2cccc(Cl)c2F)C(=O)c2cccc3cc[nH]c23)cc1
Reaction #174648
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1cc(F)ccc1Cl
Reaction #175117
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(c1cccc(Cc2n[nH]c(=O)c3ccccc23)c1)N1CCCN(c2nc3ccc(Cl)cc3s2)CC1
Reaction #175600
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CN(Cc2ccc3c(N)ncnc3c2)C(=O)C(C)N1C(=O)C=Cc1ccc(Cl)s1
Reaction #175607
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCN(Cc1ccccc1)C(=O)Cc1ccc(O)c(OC)c1
Reaction #176191
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(N)=O
Reaction #176555
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=N)C(=NOC1CC1)C(=O)OCC
Reaction #176584
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)NC(Cc1ccc(Cl)cc1)C(=O)N1CCN(c2c(Br)cnc3[nH]ncc23)CC1
Reaction #176714
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(C)C(NC(=O)OC(C)(C)C)C(=O)N1CC(O)C1
Reaction #176836
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
الصفحة 1التالي