Involved in 222 reactions

18880

CC(C)[Si](OCCC1CCC(=O)CC1)(C(C)C)C(C)C
Reaction #9393
4-(2-triisopropylsilanyloxy-ethyl)-cyclohexanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)[Si](O[C@H]1[C@H](C)OC(=O)[C@@H]1CCc1ccccc1)(C(C)C)C(C)C
Reaction #87231
(3R,4R,5S)-5-methyl-3-phenethyl-4-((triisopropylsilyl)oxy)dihydro-furan-2(3H)-one
Yield 59.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1cc(O[Si](C(C)C)(C(C)C)C(C)C)cc(-n2nc(C(C)(C)C)cc2N)c1
Reaction #88923
title compound
Yield 105.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)[Si](OCc1cc(Cl)cc(Cl)c1)(C(C)C)C(C)C
Reaction #162405
desired product
Yield 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)[Si](Oc1cc(Cl)cc(Cl)c1)(C(C)C)C(C)C
Reaction #162420
desired product
Yield 91.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)[Si](Oc1c(F)cc(C=O)cc1F)(C(C)C)C(C)C
Reaction #199161
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCc1nc(C)n(-c2ccc3c(c2)C(O[Si](C(C)C)(C(C)C)C(C)C)CC(C)(C)O3)c(=O)c1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #202703
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc([N+](=O)[O-])ccc1N1CCC(O[Si](C(C)C)(C(C)C)C(C)C)CC1
Reaction #224943
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)[Si](Oc1ccc(Br)cn1)(C(C)C)C(C)C
Reaction #228765
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)[Si](C(C)C)(C(C)C)n1ccc(-c2ccncc2)c1-c1ccc(F)cc1
Reaction #237135
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC#C[Si](C(C)C)(C(C)C)C(C)C
Reaction #253394
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C=COc1cc(CO[Si](C(C)C)(C(C)C)C(C)C)ccc1OC(F)F
Reaction #259966
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C=CCOC(=O)NC(CO[Si](C(C)C)(C(C)C)C(C)C)Cc1ccc(OCC=C)cc1
Reaction #277731
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)CC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3C(=O)C=C4C[C@@H](O[Si](C(C)C)(C(C)C)C(C)C)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #321909
3
Yield 84.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O[Si](C(C)C)(C(C)C)C(C)C)C(OC)C3)C(C)C(O[Si](C(C)C)(C(C)C)C(C)C)CC1=O)C(C)CC2OC
Reaction #335084
17-Ethyl-1-hydroxy-12-[2'-(4"-triisopropylsilyloxy-3"-methoxycyclohexyl)-1'-methylvinyl]-14-triisopropylsilyloxy-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo-[22.3.1.04,9 ]-octacos-18-ene-2,3,10,16-tetraone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O[Si](C(C)C)(C(C)C)C(C)C)C(OC)C3)C(C)C(O[Si](C(C)C)(C(C)C)C(C)C)CC1=O)C(C)CC2OC
Reaction #335414
product
Yield 89.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CC(C)[Si](C(C)C)(C(C)C)n1ccc2ccc(Br)nc21
Reaction #337871
6-bromo-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CC(C)[Si](C(C)C)(C(C)C)n1cc(C2CCN(C)CC2)c2cc(Br)ccc21
Reaction #365164
clear colorless oil
Yield 173.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CC(C)[Si](C(C)C)(C(C)C)n1ccc(-c2ccncc2)c1-c1ccc(F)cc1
Reaction #369592
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COC(=O)CC(O[Si](C(C)C)(C(C)C)C(C)C)C(NC(=O)OCc1ccccc1)C(C)C
Reaction #388289
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
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