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OC1CCCCc2ccccc21

OC1CC(NCc2ccccc2)CCc2ccccc21
Reaction #54502
5ξ-hydroxy-7-benzylamino-6,7,8,9-tetrahydro [5H] benzocycloheptene
DOI: 10.6084/m9.figshare.5104873.v1
NC1CCc2ccccc2C(O)C1
Reaction #54503
mixture
Выход 103.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1C=Cc2ccccc2CC1
Reaction #54504
7-amino-6,7-dihydro [5H] benzocycloheptene
Выход 59.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)CCCCC2(O)c1cc(OC)c(OC)c(OC)c1
Reaction #62224
32
Выход 49.6%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1CCc2ccccc2C(Oc2ccccc2Cl)C1
Reaction #178853
DOI: 10.1039/C8SC04228D
CNC1C=C(c2ccccc2)c2ccccc2CC1
Reaction #192058
DOI: 10.1039/C8SC04228D
CC1CCCc2ccccc2C1O
Reaction #197534
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccc2c(c1)C=CCCC2
Reaction #198171
DOI: 10.1039/C8SC04228D
COC(=O)C1=Cc2cc(Br)ccc2CCC1
Reaction #200909
DOI: 10.1039/C8SC04228D
Cl
Reaction #243934
DOI: 10.1039/C8SC04228D
CNC1CCc2ccccc2C(O)C1
Reaction #249822
DOI: 10.1039/C8SC04228D
CNC1C=Cc2ccccc2CC1
Reaction #265858
DOI: 10.1039/C8SC04228D
CN(C)C1CCc2ccccc2C(O)C1
Reaction #266154
DOI: 10.1039/C8SC04228D
CNC1CCc2ccc([N+](=O)[O-])cc2C(O)C1
Reaction #349712
3-nitro-7-methylamino-6,7,8,9-tetrahydro [5H] benzocycloheptene-5-ol
Выход 75.4%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc2c(c1)C(O)CC(NCc1ccccc1)CC2
Reaction #361237
7-benzylamino-3-nitro-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-ol
Выход 29.1%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc2c(c1)C=CC(NCc1ccccc1)CC2
Reaction #361238
N-benzyl-6,7-dihydro-2-nitro-5H-benzocyclohepten-7-amine
Выход 50.7%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc2c(c1)C(O)CCCC2
Reaction #361244
3-nitro-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-ol
Выход 96.3%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc2c(c1)C=CCCC2
Reaction #361245
2-nitro-6,7-dihydro-5H-benzocycloheptene
Выход 74.5%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc2c(c1)C(O)CC(NCc1ccccc1)CC2
Reaction #381723
DOI: 10.1039/C8SC04228D
CN(C)C1C=C(c2ccccc2)c2ccccc2CC1
Reaction #382692
DOI: 10.1039/C8SC04228D
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