مشارك في 65 تفاعل

18143

COC(=O)c1cc(-c2ccc(OC)c(F)c2)nn(CC2CCCC2)c1=O
Reaction #8098
title compound
المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#Cc1cccc(Cn2c(-c3ccc(Cl)cc3OCC3CCCC3)nc3cc(F)c(F)cc32)c1
Reaction #178487
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1ccc(Cn2c(-c3ccc(Cl)cc3OCC3CCCC3)nc3cc(F)c(F)cc32)c(F)c1
Reaction #193935
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)COc1ccc(Cn2c(-c3ccc(Cl)cc3OCC3CCCC3)nc3cc(F)c(F)cc32)cc1
Reaction #200974
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1nc(SCC2CCCC2)n[nH]1
Reaction #241664
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#Cc1ccc(Cn2c(-c3ccc(Cl)cc3OCC3CCCC3)nc3cc(F)c(F)cc32)cc1
Reaction #260172
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)CCCCCn1c(-c2ccc(Cl)cc2OCC2CCCC2)nc2cc(F)c(F)cc21
Reaction #273313
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
OCCNCC1CCCC1
Reaction #363549
N-cyclopentylmethyl-N-(2-hydroxyethyl)amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
OCCNCC1CCCC1
Reaction #363552
N-cyclopentylmethyl-N-(2-hydroxyethyl)amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
OCCNCC1CCCC1
Reaction #363555
N-cyclopentylmethyl-N-(2-hydroxyethyl)amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
OCCNCC1CCCC1
Reaction #363558
N-cyclopentylmethyl-N-(2-hydroxyethyl)amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
OCCNCC1CCCC1
Reaction #363561
N-cyclopentylmethyl-N-(2-hydroxyethyl)amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
OCCNCC1CCCC1
Reaction #363564
N-cyclopentylmethyl-N-(2-hydroxyethyl)amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
COC(=O)C1CCC(Cn2c(-c3ccc(Cl)cc3OCC3CCCC3)nc3cc(F)c(F)cc32)CC1
Reaction #369800
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1ccc(C=O)c(OC)c1C1CCCC1
Reaction #444145
3-cyclopentyl- methoxy- 4-methoxybenzaldehyde
المردود 73.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
O=S(=O)([O-])CC1CCCC1.[Na+]
Reaction #484863
sodium cyclopentylmethanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
Cc1nn(CC2CCCC2)c2nc(-c3ccncc3)nc(N)c12
Reaction #574464
1-cyclopentylmethyl-3-methyl-6-(4-pyridyl)-pyrazolo[3,4-d] -pyrimidin-4-amine
المردود 26.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_03
COC(=O)C(C)(CC1CCCC1)c1ccccc1
Reaction #581783
product
المردود 184.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
COC(=O)c1cccc(Cn2c(-c3ccc(Cl)cc3OCC3CCCC3)nc3cc(F)c(F)cc32)c1
Reaction #924957
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
c1cn(CC2CCCC2)cn1
Reaction #981706
1-(cyclopentylmethyl)imidazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_08
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