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943487

COc1ccc(C(=O)C2CCCC2)c(C(=O)O)c1
Reaction #58271
2-cyclopentanecarbonyl-5-methoxybenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(C3CCCC3)n[nH]c(=O)c2c1
Reaction #58272
4-Cyclopentyl-7-methoxy-2H-phthalazin-1-one
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@@H]3c4ccc(C(=O)O)cc4CC[C@H]3[C@@H]1CC[C@@H]2C(=O)c1ccc2c(c1)OCO2
Reaction #81729
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@@H]3c4ccc(C(=O)O)cc4CC[C@H]3[C@@H]1CC[C@@H]2C(=O)c1ccc2c(c1)OCO2
Reaction #81730
title compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
COCOc1ccc(C(=O)C2CCCC2c2cc(OCOC)cc(C(C)(C)O[SiH2]C(C)(C)C)c2OCOC)cc1
Reaction #199446
DOI: 10.1039/C8SC04228D
CC12CCC3c4ccc(C(=O)O)cc4CCC3C1CCC2C(=O)c1ccc2c(c1)OCO2
Reaction #394155
DOI: 10.1039/C8SC04228D
COc1ccc(C(=O)C2CCCC2)cc1
Reaction #571524
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(O)cc1)C1CCCC1
Reaction #571525
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(OCc2ccc3ccccc3n2)cc1)C1CCCC1
Reaction #571526
title compound
DOI: 10.6084/m9.figshare.5104873.v1
ON=C(c1ccc(OCc2ccc3ccccc3n2)cc1)C1CCCC1
Reaction #571527
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1C[C@H]2[C@@H](C1)c1cc(O)ccc1O[C@H]2c1ccc(O)cc1
Reaction #819486
4-(4-Hydroxy-phenyl)-2-methyl-1,2,3,3a,4,9b-hexahydro-cyclopenta[c]chromen-8-ol
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)C2CCCC2)cc1OC
Reaction #963381
dark brown oil
Ausbeute 116.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC2CCCC2)cc1OC
Reaction #963382
pale brown oil
Ausbeute 98.7%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(COc2ccc3c(C4CCCC4)n[nH]c3c2)cc1
Reaction #1098657
expected product
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)C2CCCC2)cc1OC
Reaction #1137659
dark brown oil
Ausbeute 116.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC2CCCC2)cc1OC
Reaction #1137660
pale brown oil
Ausbeute 98.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(OCCCc2c[nH]cn2)cc1)C1CCCC1
Reaction #1154871
Cyclopentyl 4-(3-(1H-imidazol-4-yl)propyloxy)phenyl ketone
DOI: 10.6084/m9.figshare.5104873.v1
COCOc1ccc(C(=O)C2CCCC2c2cc(OCOC)cc(C(C)(C)O[SiH2]C(C)(C)C)c2OCOC)cc1
Reaction #1266654
subtitled product
Ausbeute 76.4%DOI: 10.6084/m9.figshare.5104873.v1
COCOc1ccc(C(=O)C2CCCC2c2cc(C=O)cc(OC(OC)OC)c2)cc1
Reaction #1266655
subtitled product
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2c(cc(OCc3nnn[nH]3)c(Cl)c2Cl)CC12CCCC2
Reaction #1370435
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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