بحث البنية الفرعية

F[P-](F)(F)(F)(F)F

CON(C)C(=O)CCCc1c[nH]c2ccccc12
Reaction #979
amide
المردود 94.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CC(=O)N[C@@H]1CCc2ccccc2NC1=O)NC(=O)OC(C)(C)C
Reaction #1832
product
المردود 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1(c2ccccc2)CCN(CCOC(CN(C)C(=O)Cc2ccccc2)c2ccc(Cl)c(Cl)c2)CC1.CC(=O)NC1(c2ccccc2)CCN(CCOC(CN(C)C(=O)Cc2ccccc2)c2ccc(Cl)c(Cl)c2)CC1.Cl.Cl.O
Reaction #1939
hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(C)(C)C(=O)N[C@H](CCc1ccccc1)C(=O)OCc1ccccc1
Reaction #2007
(R)-α-[(2-t-Butoxycarbonylamino-2-methyl-1-oxopropyl)amino]benzenebutanoic acid benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CC(=O)N[C@H](CCc1ccccc1)C(=O)OCc1ccccc1)NC(=O)OC(C)(C)C
Reaction #2008
(R)-α-[(3-t-Butoxycarbonylamino-3-methyl-1-oxobutyl)amino]benzenebutanoic acid benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)[C@@H](CCc1ccccc1)NC(=O)C(C)(C)NC(=O)OCc1ccccc1
Reaction #2011
desired product
المردود 69.7%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)[C@@H](CCc1ccccc1)NC(=O)CC(C)(C)NC(=O)OCc1ccccc1
Reaction #2012
desired product
المردود 59.7%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)[C@@H](CCc1ccccc1)NC(=O)CCC(C)(C)NC(=O)OCc1ccccc1
Reaction #2013
(R)-α-[(4-Benzyloxycarbonylamino-4-methyl-1-oxopentyl)amino]benzenebutanoic acid allyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)C(C)(C)NC(=O)OCc1ccccc1
Reaction #2015
desired product
المردود 84.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN(C)C(=O)c1ccc(N2CCNCC2c2ccncc2)cc1
Reaction #2335
ethyl N-(4-[(4-pyridyl)piperazin-1-yl]benzoyl)-N-methylglycinate
DOI: 10.6084/m9.figshare.5104873.v1
F[P-](F)(F)(F)(F)F.F[P-](F)(F)(F)(F)F.O=C(O)c1ccnc(-c2cc(C(=O)O)ccn2)c1.[Ru+2].c1ccc(-c2ccccn2)nc1.c1ccc(-c2ccccn2)nc1
Reaction #2776
hexafluorophosphate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)cc(OC)c1NC(=O)CNC(=O)OC(C)(C)C
Reaction #3019
N-tert-butyloxycarbonyl-[(2,6-dimethoxy-4-methylphenyl)carbamoyl]methylamine
المردود 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cn1c(C(=O)NCC(=O)N(CCC(C)C)c2c(OC)cc(C)cc2OC)cc2ccccc21
Reaction #3020
methyl{2-[[(2,6-dimethoxy-4-methylphenyl)(isopentyl)carbamoyl]methylcarbamoyl]-1-indolyl}acetate
المردود 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)cc(OC)c1N(CC1CCCCC1)C(=O)CNC(=O)c1cc2ccccc2n1CCC#N
Reaction #3021
3-{2-[[(cyclohexylmethyl)(2,6-dimethoxy-4-methylphenyl)carbamoyl]methylcarbamoyl]-1-indolyl}propionitrile
المردود 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cn1c(C(=O)N[C@H](CCCCNC(=O)C=Cc2ccccc2)C(=O)NCCCCCc2c(OC)cc(C)cc2OC)cc2ccccc21
Reaction #3024
methyl (R)-{2-[N-{1-[(2,6-dimethoxy-4-methylphenyl)pentylcarbamoyl]-5-(cinnamoylamino)pentyl}carbamoyl]indol-1-yl}acetate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCC1(Cc2cc(N=Nc3ccc([N+](=O)[O-])cc3S(C)(=O)=O)ccc2O)COCCOCC(C)(C)COCCOC1
Reaction #5635
Compound 16
المردود 4.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC1CC1)c1ccc(F)c(NCc2cnc(Nc3ccccn3)s2)c1
Reaction #6976
title compound
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1
NCC(F)(F)CNC(=O)c1ccc(F)c(NCc2cnc(Nc3ccccn3)s2)c1
Reaction #6980
title compound
المردود 65.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CC(=O)NC1CCCN(C(=O)[C@H](C)N2CC[C@H](NS(=O)(=O)c3ccc4cc(Cl)ccc4c3)C2=O)C1
Reaction #7399
title compound
المردود 115.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCc1ccccc1
Reaction #7767
acetic acid benzyl ester
المردود 215.4%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي