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

COc1cc(OC)c(C2OCCO2)cc1B1OC(C)(C)C(C)(C)O1
Reaction #10759
2-(5-[1,3]dioxolan-2-yl-2,4-dimethoxy-phenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane
收率 92.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(/C=C/B1OC(C)(C)C(C)(C)O1)OCC
Reaction #45472
title compound
收率 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1(C)OB(/C=C/c2cccc(F)c2)OC1(C)C
Reaction #62309
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1ccc(Cn2cc(B3OC(C)(C)C(C)(C)O3)c(-c3cccc([N+](=O)[O-])c3)n2)cc1
Reaction #74159
title compound
收率 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC1(C)OB(c2ccc3c(c2)CC[C@H](CO[Si](C)(C)C(C)(C)C)O3)OC1(C)C
Reaction #75951
tert-butyl(dimethyl)silyl [(2R)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydro-2H-chromen-2-yl]methyl ether
收率 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COC(=O)c1c(-c2nc(C)ncc2C)cnn1C
Reaction #88414
title compound
收率 110.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(=O)N[C@@]1(C(=O)NC(C)(C)C)CCC[C@@H]1CCCB1OC(C)(C)C(C)(C)O1
Reaction #89625
(1S,2S)-1-acetamido-N-tert-butyl-2-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propyl) cyclopentanecarboxamide
收率 78.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(=O)N[C@@]1(C(=O)NC(C)(C)C)CCO[C@@H]1CCCB1OC(C)(C)C(C)(C)O1
Reaction #89628
(2R,3S)-3-acetamido-N-tert-butyl-2-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propyl)tetrahydrofuran-3-carboxamide
收率 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(=O)N[C@@]1(C(=O)NC(C)(C)C)CN(C(=O)OC(C)(C)C)C[C@@H]1CCCB1OC(C)(C)C(C)(C)O1
Reaction #89633
(3R,4S)-tert-butyl 3-acetamido-3-(tert-butylcarbamoyl)-4-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propyl)pyrrolidine-1-carboxylate
收率 82.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC1(C)OB(c2ccc(-n3c(=O)n(COCC[Si](C)(C)C)c4cccnc43)cc2)OC1(C)C
Reaction #169705
3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1-{[2-(trimethylsilyl)ethoxy]methyl}-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)c1cc2cccc(B3OC(C)(C)C(C)(C)O3)c2[nH]1
Reaction #186882
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1ccc(B2OC(C)(C)C(C)(C)O2)cc1
Reaction #199223
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(B2OC(C)(C)C(C)(C)O2)cs1
Reaction #217608
title compound ( D38 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CN1CCN(c2cccc(B3OC(C)(C)C(C)(C)O3)c2)CC1
Reaction #221184
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCOc1ccc(OC)cc1B1OC(C)(C)C(C)(C)O1
Reaction #223873
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1(C)OB(C=Cc2ccc(CN3CCOCC3)cc2)OC1(C)C
Reaction #224844
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(COCC(=O)OC(C)(C)C)cc1B1OC(C)(C)C(C)(C)O1
Reaction #242911
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1(C)OB(C=Cc2cccnc2)OC1(C)C
Reaction #273142
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc(C)c(B2OC(C)(C)C(C)(C)O2)c(N)c1
Reaction #286254
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1ccc(-c2cc(OC)ccc2F)c(B2OC(C)(C)C(C)(C)O2)c1
Reaction #298835
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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