2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Cc1cc(B2OC(C)(C)C(C)(C)O2)sc1CO[Si](C(C)C)(C(C)C)C(C)C
Reaction #9769
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC1(C)OB(c2ccc(N(c3ccccc3)c3ccccc3)cc2)OC1(C)C
Reaction #11284
N,N-diphenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
Ausbeute 72.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cc2cc(B3OC(C)(C)C(C)(C)O3)ccc2[nH]1
Reaction #45442
desired product
Ausbeute 63.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cn1cc(B2OC(C)(C)C(C)(C)O2)c(-c2ccc(F)cc2)n1
Reaction #70155
3-(4-fluorophenyl)-1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOCn1nccc1B1OC(C)(C)C(C)(C)O1
Reaction #74606
title compound
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
OB(O)c1ccc(C2OCCO2)c(C(F)(F)F)c1
Reaction #157506
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC1(C)OB(c2ccc(Cl)c(F)c2F)OC1(C)C
Reaction #171448
2-(4-chloro-2,3-difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCCCCCCc1ccc(B2OC(C)(C)C(C)(C)O2)cc1
Reaction #176569
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cn1nccc1B1OC(C)(C)C(C)(C)O1
Reaction #176735
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)n1cc(B2OC(C)(C)C(C)(C)O2)cc1C(=O)OCc1ccccc1
Reaction #177916
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1c(B2OC(C)(C)C(C)(C)O2)n(C(=O)OC(C)(C)C)c2ccccc12
Reaction #185256
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC1(COCCCCCCc2ccc(B3OC(C)(C)C(C)(C)O3)s2)COC1
Reaction #190581
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cn1nccc1B1OC(C)(C)C(C)(C)O1
Reaction #195850
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOCn1nccc1B1OC(C)(C)C(C)(C)O1
Reaction #239105
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1(C)OB(c2ccc(Cl)c(F)c2F)OC1(C)C
Reaction #241564
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1(C)OB(c2cc(F)c(Cl)cc2F)OC1(C)C
Reaction #245665
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1(C)CCN(c2cccc(B3OC(C)(C)C(C)(C)O3)c2)C1
Reaction #265106
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCC1(COCCCCCCc2ccc(-c3ccc(B4OC(C)(C)C(C)(C)O4)s3)s2)COC1
Reaction #267602
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CN1CCN(c2ccc(B3OC(C)(C)C(C)(C)O3)cc2)CC1
Reaction #303895
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Cn1c(B2OC(C)(C)C(C)(C)O2)cc2cccnc21
Reaction #313217
title compound
Ausbeute 11.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
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