1-iodopentane

CCCCCOCC1CCC(CN(Cc2ccccc2)S(=O)(=O)NC(=O)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)CC1
Reaction #52014
title compound
المردود 73.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCCCCN1C(=O)C2CC(c3ccc([N+](=O)[O-])cc3)(C2)C1=O
Reaction #63370
1-(4-nitrophenyl)-3-n-pentyl-3-azabicyclo[3.1.1]heptane-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCCCCOC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #170119
title compound
المردود 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCCCNc1c(F)c(C)c(F)c2oc(-c3ccc(N(CCC)C(C)=O)c(F)c3)cc(=O)c12
Reaction #189333
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCOc1ccc(-c2ccc(Br)cc2)cc1
Reaction #207716
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCn1cnc2c1c(=O)[nH]c(=O)n2CCCCC
Reaction #229274
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCc1ccc(NS(=O)(=O)C(C)(C)C)s1
Reaction #234230
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCN1C(=O)C2(COc3cc4c(cc32)OCCO4)c2c(Br)cccc21
Reaction #256559
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCC1(C(=O)O)CC2=C(C1)C(C)(C)CCC2(C)C
Reaction #258788
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCn1nc(-c2ccc(OC)cc2)c2cccc(Cl)c21
Reaction #264172
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCNC(=O)N(C)c1cccc(-c2ccc(CCC(=O)OC)cc2OCCCCC)c1
Reaction #296117
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCNc1ccc(C(=O)OC)cc1
Reaction #301626
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCC(C(=O)OCC)c1ccc([N+](=O)[O-])cc1
Reaction #302443
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCOc1cc2c(cc1OCc1cccc(C(=O)OC)c1)C(=O)CC2
Reaction #329630
expected product
المردود 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCCCCOc1ccc2cc(C(C)C(=O)O)ccc2c1
Reaction #335364
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CCCCCn1c(=O)[nH]c(=O)c2c1ncn2Cc1ccccc1
Reaction #336944
desired product
المردود 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
C=CCn1cnc2c1c(=O)[nH]c(=O)n2CCCCC
Reaction #336951
desired product
المردود 45.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CCCCCCCNC(=O)N(C)c1cccc(-c2ccc(CCC(=O)OC)cc2OCCCCC)c1
Reaction #338088
methyl 3-[3′-(3-heptyl-1-methylureido)-2-pentyloxybiphenyl-4-yl]propanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CCCCCNC(=O)N(C)c1cccc(-c2ccc(CCC(=O)OC)cc2OCCCCC)c1
Reaction #338093
methyl 3-[3′-(1-methyl-3-pentylureido)-2-pentyloxybiphenyl-4-yl]propanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CCCCCN1CC=C(C)CC1C(C)(C)c1ccc(OC)cc1
Reaction #348797
1,2,3,6-tetrahydro-1-pentyl-2-[1-(4-methoxyphenyl)-1-methylethyl]-4-methylpyridine
المردود 75.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_08
الصفحة 1التالي