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COC1=CCCCCC1

COCCCc1nc(C(F)F)ccc1C(=O)OC1=CC(=O)C2CCC1C2
Reaction #48277
6-Difluoromethyl-2-(3-methoxy-propyl)-nicotinic acid 4-oxo-bicyclo[3.2.1]oct-2-en-2-yl ester
Ausbeute 100.1%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(C(=O)C2=C(O)C3CCC(C3)C2=O)c([N+](=O)[O-])c1
Reaction #52570
4-hydroxy-3-(4-methanesulfonyl-2-nitrobenzoyl)-bicyclo[3.2.1]oct-3-en-2-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(C(F)(F)F)ccc1C(=O)OC1=CC(=O)C2CCC1C2
Reaction #52572
2-methyl-6-trifluoromethylnicotinic acid 4-oxobicyclo[3.2.1]oct-2-en-2-yl ester
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(C(=O)OC2=CC(=O)C3CCC2C3)c(Cl)c1Cl
Reaction #52573
2,3-Dichloro-4-methanesulfonylbenzoic acid 4-oxobicyclo[3.2.1]oct-2-en-2-yl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=C(OCc2cnc(-c3ccc(Cl)cc3)[se]2)C2CCC1C2
Reaction #74181
4-[2-(4-chlorophenyl)selenazol-5-ylmethoxy]bicyclo[3.2.1]oct-3-en-2-one
Ausbeute 63.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=C(OCc2cnc(Br)s2)C2CCC1C2
Reaction #74182
4-(2-bromothiazol-5-ylmethoxy)bicyclo[3.2.1]oct-3-en-2-one
Ausbeute 81.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(OC1=CC(=O)C2CCC1C2)c1cnc(-c2ccc(Cl)cc2)s1
Reaction #74186
4-{1-[2-(4-chlorophenyl)thiazol-5-yl]ethoxy}bicyclo[3.2.1]oct-3-en-2-one
Ausbeute 74.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCl)OC1=CC(=O)C2CCC1C2
Reaction #74187
chloro-acetic acid 4-oxo-bicyclo[3.2.1]oct-2-en-2-yl ester
Ausbeute 86.7%DOI: 10.6084/m9.figshare.5104873.v1
CCc1sc(-c2ccc(Cl)cc2)nc1C1=C(OC(=O)C(C)(C)C)C2CCC(C2)C1=O
Reaction #74189
2,2-dimethylpropionic acid 3-[2-(4-chlorophenyl)-5-ethylthiazol-4-yl]-4-oxobicyclo[3.2.1]oct-2-en-2-yl ester
Ausbeute 81.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2ccccc2)cc(C)c1C1=C(OC(=O)C(C)(C)C)C2CCC(C2)C1=O
Reaction #159487
3-(3,5-dimethylbiphen-4-yl)-4-oxo-bicyclo[3.2.1]oct-2-en-2-yl 2,2-dimethylpropionate
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(-c2ccc(Cl)cc2Cl)cc1C1=C(OC(=O)OC)C2CCC(C2)C1=O
Reaction #159488
carbonic acid 3-(2′,4′-dichloro-4-ethylbiphen-3-yl)-4-oxo-bicyclo[3.2.1]oct-2-en-2-yl ester methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)OC2=CC(=O)C3CCC2C3)ccc(C(F)(F)F)c1S(C)=O
Reaction #236849
DOI: 10.1039/C8SC04228D
CC(C)COC1=CC(=O)CCCC1
Reaction #271768
DOI: 10.1039/C8SC04228D
COCCOCc1nc(C(F)(F)F)ccc1C(=O)OC1=CC(=O)C2CCC1C2
Reaction #282575
DOI: 10.1039/C8SC04228D
COC1=CCCCCC1
Reaction #282583
DOI: 10.1039/C8SC04228D
CCc1sc(-c2ccc(Cl)cc2)nc1C1=C(OC(=O)C(C)(C)C)C2CCC(C2)C1=O
Reaction #396029
DOI: 10.1039/C8SC04228D
COCCOCc1nc(C(F)(F)F)ccc1C(=O)OC1=CC(=O)C2CCC1C2
Reaction #402447
DOI: 10.1039/C8SC04228D
Fc1cccc2c1C1(c3ccc(OCc4ccccc4)cc3)CCCCC=C1O2
Reaction #510064
title compound 22
DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(C23CCCCC=C2Oc2cccc(F)c23)cc1
Reaction #510065
title product
Ausbeute 69.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC1=CC(C)(C)CC(C)CC1
Reaction #530280
3,3,5-trimethyl-cyclohepten-1-yl ethyl ether
DOI: 10.6084/m9.figshare.5104873.v1
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