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3786

COc1ccc2c(c1)C(C)(C)CCC2=O
Reaction #52343
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(=O)c2ccc(O)cc21
Reaction #52344
title compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccc(O)cc2CCC1c1ccccc1
Reaction #59499
6-Hydroxy-2-phenyl-3,4-dihydro-2H-naphthalen-1-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccc(Oc3ccc([N+](=O)[O-])cn3)cc2CCC1c1ccccc1
Reaction #59502
6-(5-Nitro-pyridin-2-yloxy)-2-phenyl-3,4-dihydro-2H-naphthalen-1-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1OC(C)C)CCCC2=O
Reaction #62227
35
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C1CCCc2c1ccc(OC)c2OC(C)C
Reaction #62228
36
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCc2cc(OC)ccc2C1=O
Reaction #63941
ester
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1O)/C(=N/OCc1ccc([N+](=O)[O-])cc1)CCC2
Reaction #70226
title compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1O)/C(=N/OCc1ccc3nonc3c1)CCC2
Reaction #70231
title compound
Ausbeute 9.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)CCC(CC#N)C2=O
Reaction #74788
2-cyanomethyl-6-methoxy-1-tetralone
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)C(C)(C)CCC2=O
Reaction #79908
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(=O)c2ccc(O)cc21
Reaction #79909
title compound
Ausbeute 52.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1OC)CC(c1ccccc1)CC2=O
Reaction #82396
5,6-dimethoxy-3-phenyl-1,2,3,4-tetrahydronaphthalen-1-one
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1OC)CC(c1ccccc1)CC2=O
Reaction #82399
5,6-dimethoxy-3-phenyl-1,2,3,4-tetrahydronaphthalen-1-one
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1OC)CC(c1ccccc1)CC2(O)CN
Reaction #82400
title compound
Ausbeute 73.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1OC)CC(C1CCCCC1)CC2=O
Reaction #82408
3-cyclohexyl-5,6-dimethoxy-1,2,3,4-tetrahydronaphthalen-1-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1OC)CC(C1CCCCC1)CC2(O)CN
Reaction #82409
1-aminomethyl-5,6-dimethoxy-1-hydroxy-3-cyclohexyl-1,2,3,4-tetrahydronaphthalene
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1C(=O)c2ccc(OC)c(OC)c2CC1c1ccccc1
Reaction #82413
title compound
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1OC)CC(c1ccccc1)C=C2C#N
Reaction #82420
title compound
Ausbeute 83.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCc2cc(OCCC(F)(F)F)ccc21
Reaction #91359
title compound
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1
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