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1250630

c1cncc(-c2ccc(-c3c4ccccc4c(-c4ccc(-c5cccnc5)nc4)c4ccccc34)cn2)c1
Reaction #308359
9,10-bis(2,3′-bipyridine-5-yl)anthracene
DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(C)cnc1N(C(=O)OCC(C)C)S(=O)(=O)c1cccnc1-c1ccc(-c2ncccn2)cc1
Reaction #448634
N-isobutoxycarbonyl-N-(3-methoxy-5-methylpyrazin-2-yl)-2-(4-[pyrimidin-2-yl]phenyl)pyridine-3-sulphonamide
Ausbeute 17.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccccc1-c1ccc(-c2ccccc2C(=O)OC)c2ccccc12
Reaction #490319
1,4-Bis(2-methoxycarbonylphenyl)naphthalene
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(C(=O)OCc3ccccc3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(B(O)O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #494077
(4-((1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR,13bR)-3a-((benzyloxy)carbonyl)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-octadecahydro-1H-cyclopenta[a]chrysen-9-yl)phenyl)boronic acid
Ausbeute 34.2%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(-c2ccc(-c3ccc(C=O)o3)cc2)o1
Reaction #509301
11
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(-c2ccc(-c3ccc(C#N)cc3)cc2)cc1
Reaction #509303
17
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(-c3ncccn3)cc2)OC1(C)C
Reaction #555825
title compound
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1
CCn1nc(-c2ccc(-c3nn(CC)c4cccnc34)cc2)c2ncccc21
Reaction #660469
title compound
Ausbeute 7.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)c2ccccc2-c2cccc(-c3ccc(-c4cccc5c4C(C)(C)c4ccccc4-5)cc3)c21
Reaction #725956
1,4-phenylenebis(9,9-dimethylfluorene)
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2cc3c(ccc4c(-c5ccc(-c6cccc7c6ccc6cc8ccccc8cc67)cc5)cccc43)cc2c1
Reaction #964472
1,4-bis(benz[a]anthracen-4-yl)benzene
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(-c3ccc(CS(C)(=O)=O)cc3)cc2)OC1(C)C
Reaction #1137419
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(-c2ccc(B3OC(C)(C)C(C)(C)O3)cc2)cc1)NC(=O)OC(C)(C)C
Reaction #1137428
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(-c3nc4nc(O[C@H]5CO[C@@H]6COC(c7ccccc7)O[C@H]6C5)n(COCC[Si](C)(C)C)c4cc3Cl)cc2)OC1(C)C
Reaction #1137434
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(-c2ccc(-c3ccc(Br)c4nn(-c5ccncc5)nc34)cc2)c2nn(-c3ccncc3)nc12
Reaction #1137863
Intermediate G
DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(C)cnc1N(C(=O)OCC(C)C)S(=O)(=O)c1cccnc1-c1ccc(-c2ncccn2)cc1
Reaction #1471418
N-isobutoxycarbonyl-N-(3-methoxy-5-methylpyrazin-2-yl)-2-(4-[pyrimidin-2-yl]phenyl)pyridine-3-sulphonamide
Ausbeute 17.9%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(-c3nc4c(cc3Cl)nc(O[C@@H]3CO[C@H]5[C@@H]3OC[C@H]5O)n4COCC[Si](C)(C)C)cc2)OC1(C)C
Reaction #1572787
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(-c3ncccn3)cc2)OC1(C)C
Reaction #1712221
title compound
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(-c2ccc(-c3ccc(C=O)o3)cc2)o1
Reaction #2017677
11
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(-c2ccc(-c3ccc(C#N)cc3)cc2)cc1
Reaction #2017679
17
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1ccc(-c2ccc(C(=O)OCCCC)cc2-c2ccccc2)cc1
Reaction #2460307
dibutyl 4,4′-terphenyl dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
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