Recherche de Sous-structure

Brc1ccc(OCc2ccccc2)cc1

C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(OCc2ccccc2)cc1
Reaction #202
Rendement 35.7%
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(OCc2ccccc2)cc1
Reaction #203
Rendement 0.0%
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(OCc2ccccc2)cc1
Reaction #204
Rendement 31.5%
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1ccc(OCc2ccccc2)cc1
Reaction #205
Rendement 0.0%
C[C@H](CNc1ccc(OCc2ccccc2)cc1)O[Si](C)(C)C(C)(C)C
Reaction #434
Rendement 65.2%
C[C@H](CNc1ccc(OCc2ccccc2)cc1)O[Si](C)(C)C(C)(C)C
Reaction #435
Rendement 18.9%
COc1cc(OCc2ccccc2)ccc1Br
Reaction #1903
4-benzyloxy-2-methoxybromobenzene
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CN(c2ccncc2)CCN1c1ccc(OCc2ccccc2)cc1
Reaction #2348
4-benzyloxy [4-(4-pyridyl)piperazin-2-one-1-yl]benzene
Rendement 123.3%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(OCc2ccccc2)cc1
Reaction #11297
4-benzyloxybromobenzene
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(Nc2ccc(Cl)cc2)cc(-c2cc(Br)ccc2OCc2ccc([N+](=O)[O-])cc2)n1
Reaction #56934
title compound
Rendement 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1COc1ccc(Br)cc1-c1cc(Nc2ccc(Cl)cc2)nc(N)n1
Reaction #56935
title compound
Rendement 57.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1COc1ccc(Br)cc1-c1cc(Nc2ccc(C)cc2)nc(N)n1
Reaction #56940
title compound
Rendement 36.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)Cc1cc(Br)ccc1OCc1ccccc1
Reaction #59776
2-benzyloxy-5-bromo-phenylacetic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(C(F)(F)F)c(OCc2ccccc2)cc1OCc1ccccc1)N1Cc2ccccc2C1
Reaction #69709
title compound
Rendement 29.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C=Cc1cc(Br)ccc1OCc1ccccc1
Reaction #78869
3-(2-Benzyloxy-5-bromophenyl)-acrylic Acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OCCC(c2ccccc2)c2cc(Br)ccc2OCc2ccccc2)cc1
Reaction #78871
(±)-toluene-4-sulphonic acid 3-(2-benzyloxy-5-bromophenyl)-3-phenylpropyl ester
Rendement 93.6%DOI: 10.6084/m9.figshare.5104873.v1
OC1(c2ccc(OCc3ccccc3)cc2)CCOCC1
Reaction #79367
4-(4-benzyloxyphenyl)tetrahydro-2H-pyran-4-ol
Rendement 55.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Br)c(C=O)cc1OCc1ccccc1
Reaction #160510
title compound
Rendement 74.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)/C(=C/c1cc(OCc2ccccc2)c(C)cc1Br)NC(=O)OCc1ccccc1
Reaction #160511
title compound
Rendement 58.1%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cc(Br)ccc1OCc1ccccc1
Reaction #188239
DOI: 10.1039/C8SC04228D
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