Recherche de Sous-structure

CC(C)(C)[Si](C)(C)Cl

CC(C)(C)[Si](OCc1ccc(CCCC2OCCO2)cc1)(c1ccccc1)c1ccccc1
Reaction #986
171
Rendement 102.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OCc1ccc(CCCC=O)cc1)(c1ccccc1)c1ccccc1
Reaction #987
aldehyde
Rendement 42.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(Cc1ccc(Br)cc1)O[Si](C)(Cc1ccc(Br)cc1)C(C)(C)C
Reaction #1133
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1cc2ccc(Br)cc2cc1C12CC3CC(CC(C3)C1)C2
Reaction #1239
7-(1-adamantyl)-6-tert-butyldimethylsilyloxy-2-bromonaphthalene
DOI: 10.6084/m9.figshare.5104873.v1
ClCCl.N
Reaction #1246
NH3 CH2Cl2
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(O[Si](C)(C)C(C)(C)C)c2cc(Br)ccc21
Reaction #1455
Compound B15
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OC1C=CC(=O)C1
Reaction #2634
title compound
Rendement 83.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(C#N)cc1CN1CC[C@H](NS(=O)(=O)c2ccc(-c3cccnc3)s2)C1=O
Reaction #2870
oil
Rendement 74.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)O[C@@H]1CCC[C@H]1O
Reaction #3238
(trans)-2-(t-butyldimethysiloxy)-cyclopentanol
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn([C@H]2C[C@H](O)[C@@H](CO[Si](C)(C)C(C)(C)C)O2)c(=O)[nH]c1=O
Reaction #3745
5'-O-(tert-butyldimethylsilyl) thymidine
Rendement 70.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC[C@H]2O[C@@H](n3cc(C)c(=O)[nH]c3=O)C[C@@H]2O[Si](C)(C)C(C)(C)C)(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #3747
5'-O-(4,4'-dimethoxytrityl)-3'-O-(tert-butyldimethlsilyl) thymidine
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC=C(C)CCC=C(C)CO[Si](C)(C)C(C)(C)C
Reaction #5750
1-acetoxy-8-(dimethyl t-butylsilyl)oxy-3,7-dimethyl-2,6-octadiene
Rendement 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OCc1ccc(CBr)cc1
Reaction #6023
title compound
Rendement 71.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCc1cc(C(=O)OC)cc(CC=C)c1O[Si](C)(C)C(C)(C)C
Reaction #6026
title compound
Rendement 97.2%DOI: 10.6084/m9.figshare.5104873.v1
CON=C1CC(CO[Si](C)(C)C(C)(C)C)(CO[Si](C)(C)C(C)(C)C)C1
Reaction #6061
title compound
Rendement 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OC1CC(NC(=O)OCc2ccccc2)C1
Reaction #6064
title compound
Rendement 94.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC[C@@H]1C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](CCCCCC)C(=O)O1
Reaction #6156
(3S,4S,6R)-tetrahydro-3-hexyl-4-[(t-butyldimethylsilyl)oxy]-6-undecyl-2H-pyran-2-one
Rendement 63.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OC[C@@H](O)COCc1ccccc1)(c1ccccc1)c1ccccc1
Reaction #6352
title compound
Rendement 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(CC(N)=O)cc1Cl
Reaction #6822
2-[4-(tert-butyldimethylsilanyloxy)-3-chlorophenyl]acetamide
Rendement 77.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc([N+](=O)[O-])cc1
Reaction #7332
1-nitro-4-(1,1,2,2-tetramethyl-1-silapropoxy)benzene
DOI: 10.6084/m9.figshare.5104873.v1
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