Teilstruktursuche

1250774

CCc1ccc(-c2ccc(Cl)cc2)cc1B(O)O
Reaction #68744
4′-chloro-4-ethylbiphen-3-ylboronic acid
Ausbeute 69.1%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(-c2ccc(Cl)cc2)cc1C1=C(OC)CCC1=O
Reaction #68746
2-(4′-chloro-4-ethylbiphen-3-yl)-3-methoxycyclopent-2-enone
Ausbeute 75.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccc(Cl)cc2)cc1B(O)O
Reaction #71601
5-(4-chlorophenyl)-2-methylphenylboronic acid
Ausbeute 50.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccc(Cl)cc2)cc1B(O)O
Reaction #71607
5-(4-chloro-phenyl)-2-methylphenylboronic acid
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
c1cc(-c2ccc3c4ccccc4c4ccccc4c3c2)cc(-c2ccc3sc4sc5ccccc5c4c3c2)c1
Reaction #92499
white solid
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccc(Cl)cc2)cc1B(O)O
Reaction #159429
4′-chloro-4-methylbiphen-3-ylboronic acid
Ausbeute 50.7%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(-c2ccc(Cl)cc2)cc1B(O)O
Reaction #159435
4′-chloro-4-ethylbiphen-3-ylboronic acid
Ausbeute 69.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].CCc1ccc(-c2ccc(Cl)cc2)c[c]1[Pb+3]
Reaction #159436
4′-chloro-4-ethylbiphen-3-yllead triacetate
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)c1cnn2c(-c3ccc(F)c(-c4ccccc4C#N)c3)cnc2n1
Reaction #176641
DOI: 10.1039/C8SC04228D
COc1ccc(-c2ccc3cc(C=O)ccc3c2)cc1-c1ccccc1
Reaction #183313
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1ccccc1-c1cc(-c2cnc3nc(C(F)(F)F)cnn23)ccc1F
Reaction #186364
DOI: 10.1039/C8SC04228D
N#Cc1ccccc1-c1cc(-c2cnc3cc(C(F)(F)F)ncn23)ccc1F
Reaction #187661
DOI: 10.1039/C8SC04228D
CC(C)(O)c1ccn2c(-c3cccc(-c4ccc(F)cc4C#N)c3)cnc2n1
Reaction #195748
DOI: 10.1039/C8SC04228D
O=C(N1CCc2ccc(Cl)c(-c3cccc(-c4ccccc4)c3)c2CC1)C(F)(F)F
Reaction #203055
DOI: 10.1039/C8SC04228D
O=C1OC2(CCN(C(=O)c3cn(-c4cccc(-c5ccccc5)c4)c4cc(Cl)ccc34)CC2)c2ccccc21
Reaction #239180
DOI: 10.1039/C8SC04228D
N#Cc1ccccc1-c1cc(F)cc(-c2ccnc3nc(C(F)(F)F)ccc23)c1
Reaction #239950
DOI: 10.1039/C8SC04228D
Cc1c(-c2cccc(-c3ccc(Cl)cc3)c2)cnc(N)c1C#N
Reaction #250899
DOI: 10.1039/C8SC04228D
N#Cc1ccc(F)c(-c2cc(-c3ccnc4nc(C(F)(F)F)ccc34)ccc2F)c1
Reaction #273926
DOI: 10.1039/C8SC04228D
N#Cc1ccc(-c2cc(-c3ccnc4nc(C(F)(F)F)ccc34)ccc2F)cc1
Reaction #275559
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(-c2ccc(OC)c(-c3ccc(C(F)(F)F)cc3CN3C(=O)OC(c4cc(C(F)(F)F)cc(C(F)(F)F)c4)C3C)c2)c(C)c1
Reaction #281037
DOI: 10.1039/C8SC04228D
Seite 1Weiter