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B(CC)(CC)CC

CN(C)Cc1ccc([C@H]2CC[C@@H](O)CC2)cc1
Reaction #1743
cis-4-(4-Dimethylaminomethylphenyl)-cyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OCC1CC(O)C1CO[Si](C)(C)C(C)(C)C
Reaction #6052
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CC(O)C1)OCc1ccccc1
Reaction #6063
title compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC1(C(O)c2cccc([C@H]3[C@H](O)CC(=O)[C@@H]3C/C=C\CCCC(=O)NCC)c2)CCC1
Reaction #9331
alcohol
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)COCC#CC[C@@H]1[C@@H](c2ccc(C(O[Si](C)(C)C(C)(C)C)C3CCCCC3)cc2)[C@H](O[Si](C)(C)C(C)(C)C)C[C@@H]1O
Reaction #9335
alcohol
Ausbeute 61.9%DOI: 10.6084/m9.figshare.5104873.v1
OCCC1CCC=C1Br
Reaction #9367
2-(2-bromo-cyclopent-2-enyl)-ethanol
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CCN1C(=O)OC(C)(C)C
Reaction #10488
title compound
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1CCC(O)N1C(=O)OC(C)(C)C
Reaction #10515
crude product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3n2C)cc1C=O
Reaction #10839
2,4-dimethoxy-5-(1-methyl-1H-indol-2-yl)-benzaldehyde
Ausbeute 25.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc2c(n1)N1[C@H](C2)CN(C(=O)OC(C)(C)C)C[C@H]1C
Reaction #12012
product
Ausbeute 89.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCCCC1=O
Reaction #40310
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cccc(CNC2CC2)c1
Reaction #42561
11
DOI: 10.6084/m9.figshare.5104873.v1
CC1CN([C@H](c2cc(F)c(F)c(F)c2)[C@@H](C)O[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)C(=O)[C@@H](O)O1
Reaction #44611
title compound
Ausbeute 97.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1CN([C@@H](C)c2ccc(F)nc2F)C(=O)[C@@H](O)O1
Reaction #44619
title compound
Ausbeute 99.7%DOI: 10.6084/m9.figshare.5104873.v1
CC1CN([C@H](c2cc(F)c(F)c(F)c2)[C@@H](C)O[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)C(=O)[C@@H](O)O1
Reaction #44639
title compound
Ausbeute 97.5%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC(CO)c1c(-c2ccccc2)c(C)c(C#N)c2nc(C3CC3)oc12
Reaction #45864
compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CC=CN1C(=O)O
Reaction #46048
4,5-dihydro-1H-pyrrole-1,5-dicarboxylic acid
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
O[C@H]1C[C@H]2CO[C@@H](C1)O2
Reaction #50185
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](C)/C=C(/C)CO
Reaction #50356
alcohol
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
O[C@H]1C[C@H]2CO[C@@H](C1)O2
Reaction #50688
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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