Поиск подструктуры

OC1CCCCc2ccccc21

CC(C)(C)[Si](Oc1cccc2c1CCCC(CO)C2O)(c1ccccc1)c1ccccc1
Reaction #392866
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccc2c(c1)C(O)CCCC2
Reaction #399936
DOI: 10.1039/C8SC04228D
CN(C)C1CCc2ccccc2C(O)C1
Reaction #459722
7-dimethylamino-5-hydroxy-6,7,8,9-tetrahydro [5H] benzocycloheptene
Выход 91.1%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1C=Cc2ccccc2CC1
Reaction #459723
7-dimethylamino-6,7-dihydro [5H] benzocycloheptene
Выход 49.3%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1CCc2ccccc2C(O)(c2ccccc2)C1
Reaction #459725
7-dimethylamino-5ξ-phenyl-5ξ-hydroxy6,7,8,9-tetrahydro [5H] benzocycloheptene
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1C=C(c2ccccc2)c2ccccc2CC1
Reaction #459726
7-dimethylamino-9-phenyl-6,7-dihydro [5H] benzocycloheptene
Выход 74.2%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1CCc2ccccc2C(c2ccccc2)C1
Reaction #459728
7-dimethylamino-5-phenyl-6,7,8,9-tetrahydro [5H] benzocycloheptene
DOI: 10.6084/m9.figshare.5104873.v1
CNC1CCc2ccccc2C(O)C1
Reaction #459730
7-methylamino-5-hydroxy-6,7,8,9-tetrahydro [5H] benzocycloheptene
Выход 104.2%DOI: 10.6084/m9.figshare.5104873.v1
CNC1C=Cc2ccccc2CC1
Reaction #459731
7-methylamino-6,7-dihydro [5H] benzocycloheptene
Выход 50.3%DOI: 10.6084/m9.figshare.5104873.v1
CNC1C=C(c2ccccc2)c2ccccc2CC1
Reaction #459733
7-methylamino-9-phenyl-6,7-dihydro [5H] benzocycloheptene
Выход 76.6%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C2CCc3ccccc3C(O)C2)CC1
Reaction #459736
mixture
Выход 101.5%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C2C=Cc3ccccc3CC2)CC1
Reaction #459737
7-(4-methylpiperazin-1-yl)-6,7-dihydro [5H] benzocycloheptene
Выход 74.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCNC1CCc2ccccc2C(O)C1
Reaction #459738
7-allylamino-5ξ-hydroxy-6,7,8,9-tetrahydro [5H] benzocycloheptene
Выход 98.4%DOI: 10.6084/m9.figshare.5104873.v1
C=CCNC1C=Cc2ccccc2CC1
Reaction #459739
7-allylamino-6,7-dihydro [5H] benzocycloheptene
Выход 79.1%DOI: 10.6084/m9.figshare.5104873.v1
OC1CC(N2CCCC2)CCc2ccccc21
Reaction #459741
5ξ-hydroxy-7-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro [5H] benzocycloheptene
Выход 97.8%DOI: 10.6084/m9.figshare.5104873.v1
CNC1CCc2ccc(Cl)cc2C(O)C1
Reaction #459742
3-chloro-5ξ-hydroxy-7-methylamino-6,7,8,9-tetrahydro [5H] benzocycloheptene
Выход 92.7%DOI: 10.6084/m9.figshare.5104873.v1
CNC1C=Cc2cc(Cl)ccc2CC1.Cl
Reaction #459743
2-chloro-7-methylamino-6,7-dihydro [5H] benzocycloheptene hydrochloride
Выход 164.9%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCCC1CCCC(C)C2=C1CC=CC2
Reaction #459995
5-diethylaminopropyl-9-methyl-1,4,6,7,8,9-hexahydro-5H-benzocycloheptene
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCCC1CCCC(C)C2=C1CC=CC2
Reaction #529246
5-diethylaminopropyl-9-methyl-1,4,6,7,8,9-hexahydro-5H-benzocycloheptene
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC=Cc2c(Br)cccc21
Reaction #749509
DOI: 10.1039/C8SC04228D
НазадСтраница 2Далее