cyclopropane

C1CC1.Oc1ccc(O)cc1
Reaction #2763
Hydroquinone cyclopropane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1ccc(C2CCCc3cncn32)c(C2CC2)c1
Reaction #164084
3-Cyclopropyl-4-(5,6,7,8-tetrahydro-imidazo[1,5-a]pyridin-5-yl)benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=CCOC1CC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CCC2C)C(OC)CC3C)CCC1NC(=O)C1CC1
Reaction #190231
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#CC(C(=S)Nc1ccc(C(F)(F)F)cc1)=C(O)C1CC1
Reaction #196553
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccccc1CNc1ccc2cc(NC(=O)C3CC3)ccc2n1
Reaction #205213
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(C1CC1)N1CCC2(c3ccccc3)Oc3ccccc3C2C1
Reaction #275111
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCOC1CC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CCC2C)C(OC)CC3C)CCC1NC(=O)C1CC1
Reaction #276257
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1c(Nc2ccc(I)cc2F)c(NS(=O)(=O)C2CC2)c2n(c1=O)CCS2
Reaction #279926
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CSc1ccc(C(Oc2ccc3c(cnn3-c3ccc(F)cc3)c2)C(C)NS(=O)(=O)C2CC2)cc1
Reaction #293932
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
N#Cc1ccc(C2CCCc3cncn32)c(C2CC2)c1
Reaction #375689
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(Nc1cccc(Br)c1)C1CC1
Reaction #405396
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(Nc1cccc(I)c1)C1CC1
Reaction #406255
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)C1=NOC(c2ccccc2)(c2ccccc2)C1
Reaction #607921
5,5-diphenylisoxazoline carboxylate ethyl ester
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CCOC(=O)C1=NOC(c2ccccc2)(c2ccccc2)C1
Reaction #607922
solid
収率 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CCOC(=O)C1=NOC(c2ccccc2)(c2ccccc2)C1
Reaction #607923
solid
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CCOC(=O)C1=NOC(c2ccccc2)(c2ccccc2)C1
Reaction #607924
solid
収率 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CC(C)(C)OC(=O)NC1=N[C@]2(C)c3cc(NC(=O)c4cnc(OCC5CC5)cn4)ccc3OCC[C@H]2S(=O)(=O)C1(C)C
Reaction #714937
title compound
収率 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
CC(C)N1CCC(Oc2cc3cc(C(=O)N4CCN(C(=O)C5CC5)CC4)[nH]c3cc2Cl)CC1
Reaction #773651
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Cc1ccc(CNc2ccc3c(NS(=O)(=O)C4CC4)cccc3n2)o1
Reaction #893557
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
O=C(Nc1ccc(OCc2ccccc2)cc1)C1CC1
Reaction #903569
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
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