imidazole

CC(C)(C)[Si](OCc1ccc(CCCC2OCCO2)cc1)(c1ccccc1)c1ccccc1
Reaction #986
171
収率 102.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)[Si](OCc1ccc(CCCC=O)cc1)(c1ccccc1)c1ccccc1
Reaction #987
aldehyde
収率 42.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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.v1uspto-grants-1998_03
O=P(O)(O)C(Cn1ccnc1)S(=O)(=O)O
Reaction #2787
2-(1-imidazolyl)-1-phosphonoethanesulfonic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)[Si](C)(C)Oc1ccc(C#N)cc1CN1CC[C@H](NS(=O)(=O)c2ccc(-c3cccnc3)s2)C1=O
Reaction #2870
oil
収率 74.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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.v1uspto-grants-1998_03
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
収率 70.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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.v1uspto-grants-1998_03
CC(C)(C)OC(=O)c1ncc[nH]1
Reaction #4523
tert-butyloxycarbonylimidazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(Cl)OC(=O)c1ncc[nH]1
Reaction #4527
α-chloroethoxycarbonylimidazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COC(=O)c1ccc2c(c1)C(NC(=O)Cn1ccnc1)c1ccccc1CO2
Reaction #5136
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
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
収率 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=C[C@H](O[Si](C(C)C)(C(C)C)C(C)C)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C
Reaction #6171
title compound
収率 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)(C)[Si](OC[C@@H](O)COCc1ccccc1)(c1ccccc1)c1ccccc1
Reaction #6352
title compound
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)(C)[Si](C)(C)Oc1ccc(CC(N)=O)cc1Cl
Reaction #6822
2-[4-(tert-butyldimethylsilanyloxy)-3-chlorophenyl]acetamide
収率 77.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)[Si](Oc1ccc2[nH]cc(CCN)c2c1)(C(C)C)C(C)C
Reaction #6842
2-(5-triisopropylsilanyloxy-1H-indol-3-yl)-ethylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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.v1uspto-grants-2006_08
COc1cc(-c2nc3ccccc3o2)ccc1Cn1ccnc1
Reaction #7839
2-[4-(1H-imidazol-1-ylmethyl)-3-methoxyphenyl]-1,3-benzoxazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)[Si](C)(C)OCCC(N)C(=O)O
Reaction #8625
2-amino-4-(tert-butyldimethylsilanyloxy)butyric acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=CC1C(O[Si](C)(C)C(C)(C)C)CCC12CCN(C(=O)OC(C)(C)C)CC2
Reaction #8858
title compound
収率 86.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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