cycloheptanone

BrC1CCCCCC12OCCO2
Reaction #999
2-bromocycloheptanone ethylene ketal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Oc1ccc(C2(c3ccc(O)cc3)CCCCCC2)cc1
Reaction #56078
4,4'-cycloheptylidenediphenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
N#Cc1ccc(C(c2ncc[nH]2)C2(O)CCCCCC2)cc1
Reaction #64187
4-[1-hydroxycyclohept-1-yl-1-(imidazolyl)methyl]benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
N#Cc1ccc(C(c2nc[nH]n2)C2(O)CCCCCC2)cc1
Reaction #64195
4-[1-hydroxycyclohept-1-yl-1-(1,2,4-triazolyl) methyl]benzonitrile
Выход 98.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
C1=C(c2ccccc2)CCCCC1
Reaction #157907
1-phenylcycloheptene
Выход 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cc(C2CCCCCC2=O)ccn1
Reaction #178557
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1CCCCCC1C(=O)COC1CCCCO1
Reaction #192972
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C(=O)O)c1ccc(C=C2CCCCCC2=O)cc1
Reaction #214194
desired product
Выход 39.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
Nc1ncnn2c(-c3cccc(CNC4CCCCCC4)c3)cc(-c3ccc4cn(Cc5ccccc5)nc4c3)c12
Reaction #242195
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Oc1cccc(C(=C2CCCCCC2)c2ccc(Br)c(F)c2)c1
Reaction #246680
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Oc1ccc(C(=C2CCCCCC2)c2ccc(O)cc2)cc1
Reaction #247002
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCC(CC)(c1ccc(O)c(C)c1)c1ccc(C#CC2(O)CCCCCC2)c(C)c1
Reaction #250191
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(NCCCCNC1CCCCCC1)c1ccc(CN(Cc2ncc[nH]2)Cc2ncc[nH]2)cc1
Reaction #268589
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C1CCCCCC12Cc1ccccc1C2
Reaction #272680
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
N#CC(=C1CCCCCC1)c1ccsc1
Reaction #273227
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C1CCCCCC1Cc1ccccc1Br
Reaction #274011
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC1CCCCCC1=O
Reaction #275038
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC1=CCCCCC1
Reaction #282583
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Oc1ccc(C(=C2CCCCCC2)c2ccc(Br)cc2)cc1
Reaction #316315
compound ( 9 )
Выход 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Oc1ccc(C(=C2CCCCCC2)c2ccc(Br)cc2)cc1Cl
Reaction #316392
compound 124
Выход 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Страница 1Далее