Teilstruktursuche

ON1CCOCC1

CCOC(=O)c1ccc2cc(-c3ccc4c(c3)C(=O)CCC4(C)C)ccc2c1
Reaction #1474
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cccc2[nH]ccc12
Reaction #6795
indole-4-aldehyde
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCC(O)CO
Reaction #8282
title compound
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)c1oc2nc(-c3ccccc3Cl)c(-c3ccc(Cl)cc3)cc2c1C=O
Reaction #8908
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCC1(C=O)CCC1
Reaction #9328
1-4
Ausbeute 218.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCC/C=C\C[C@@H]1[C@@H](c2ccc(C=O)cc2)[C@H](O[Si](C)(C)C(C)(C)C)C[C@H]1Cl
Reaction #9334
9-2
Ausbeute 79.7%DOI: 10.6084/m9.figshare.5104873.v1
O=CCC1Cc2ccccc2C1
Reaction #9372
indan-2-yl-acetaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)c3c(-c4ccccc4Cl)cc4c(c3C2=O)c2cc(OC)ccc2n4CC(O)CO)c(OC)c1
Reaction #11227
diol
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(Br)C(=O)c1cccc(Cl)c1
Reaction #11303
2-bromo-3′-chloropropiophenone
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OC1CCCC(=O)CCC1
Reaction #44489
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1c2c(c3n(c1=O)CCC(=O)CN(C)C3=O)CCN(Cc1ccc(F)c(Cl)c1)C2=O
Reaction #46301
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1c2c(c3n(c1=O)CC(CO)OC3=O)CCN(Cc1ccc(F)c(Cl)c1)C2=O
Reaction #46311
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)CCCC12CCC(c3nnc(-c4ccc(O)cc4Cl)n3C)(CC1)CC2
Reaction #51123
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OC[C@H]1O[C@@H](n2cnc3c(NC(=O)c4ccccc4)ncnc32)[C@H](OCC(O)CO)[C@@H]1O)(c1ccccc1)c1ccccc1
Reaction #51522
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](c1ccccc1)(c1ccccc1)C(O)[C@H]1O[C@@H](n2cnc3c(=O)[nH]c(N)nc32)[C@H](OCCO)[C@@]1(O)[Si](c1ccccc1)(c1ccccc1)C(C)(C)C
Reaction #51524
title compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CN(C2CC2)Cc2ccc(C=O)cc21
Reaction #52355
title compound
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(Br)C(=O)c1cccc(Cl)c1
Reaction #52551
2-bromo-3′-chloropropiophenone
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc2cc(-c3ccc4c(c3)C(=O)CCC4(C)C)ccc2c1
Reaction #52852
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCCc1ccccc1OCC(O)CO)OCc1ccccc1
Reaction #53397
Compound 31
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cccc2[nH]ccc12
Reaction #56691
indole-4-aldehyde
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter