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CC1CCOC1=O

O=C1OC(=O)C2C(Sc3ccccc3)CC12
Reaction #6072
title compound
Ausbeute 90.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]c3c(c2c1)C1C(=O)OC(=O)C1C(c1ccccc1Cl)C3
Reaction #11223
4-(2-Chlorophenyl)-9-methoxy-4,5,6,10c-tetrahydro-1H-furo[3,4-c]carbazole-1,3(3aH)-dione
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)c3c(-c4ccccc4Cl)cc4[nH]c5ccc(OC)cc5c4c3C2=O)c(OC)c1
Reaction #11224
4-(2-Chlorophenyl)-2-(2,4-dimethoxybenzyl)-9-methoxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=C(CCO)C(=O)N1
Reaction #52243
hydroxy ethylmaleimide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC=C1CCOC1=O
Reaction #65054
3-Pentylidene-dihydro-2(3H)-furanone
DOI: 10.6084/m9.figshare.5104873.v1
CC1CC(=CC2CCCCC2)C(=O)O1
Reaction #65055
3-cyclohexylmethylene-5-methyldihydro-2(3H)-furanone
Ausbeute 97.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1C/C(=C\c2ccccc2)C(=O)O1
Reaction #65056
(E)-3-(phenylmethylene)-5-butyldihydro-2 (3H)-furanone
Ausbeute 64.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1=CCC(/C=C/C2CCOC2=O)C1(C)C
Reaction #65057
(E)-3-[2-(2,2,3-trimethylcyclopent-3-en-yl)ethenyl]dihydro-2 (3H)-furanone
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1O[C@H]2C[C@@H]1CC[C@@H]2Br
Reaction #92314
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)[C@H]1CC[C@H](Br)[C@@H](O)C1
Reaction #92315
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)[C@H]1CC[C@H](Br)[C@@H](O)C1
Reaction #92319
(1S,3S,4S)-3-hydroxy-4-bromo-N,N-dimethylcyclohexanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1ccc(C(=O)SCC2C(=O)OCC2c2ccccc2)cc1
Reaction #93538
title compound
Ausbeute 79.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(SCC1C(=O)OCC1c1ccccc1)c1ccccc1F
Reaction #93540
title compound
Ausbeute 67.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OCC(c2ccccc2)C1CS
Reaction #93541
title compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(S(=O)(=O)O)CC(=O)OC1=O
Reaction #94707
SULFO-METHYL-SUCCINIC ANHYDRIDE
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])CCC(=O)[O-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #163392
triphenylsulfonium succinic acid salt
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])CCC(=O)[O-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #163393
triphenylsulfonium succinic acid salt
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])CCC(=O)[O-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #163394
triphenylsulfonium succinic acid salt
DOI: 10.6084/m9.figshare.5104873.v1
CCC1CC(c2ccccc2)C(=O)O1
Reaction #176221
DOI: 10.1039/C8SC04228D
O=C1OCCC12Sc1cc(Cl)ccc1C2=O
Reaction #182799
DOI: 10.1039/C8SC04228D
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