部分構造検索

2626

CC(C)(C)[Si](OCc1ccc(CCCC2OCCO2)cc1)(c1ccccc1)c1ccccc1
Reaction #986
171
収率 102.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OCc1ccc(CCCC=O)cc1)(c1ccccc1)c1ccccc1
Reaction #987
aldehyde
収率 42.8%DOI: 10.6084/m9.figshare.5104873.v1
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.v1
CC(C)(C)[Si](OC(CC#N)c1ccncc1)(c1ccccc1)c1ccccc1
Reaction #11555
3-(t-butyldiphenylsiloxy)-3-(4-pyridyl)propionitrile
収率 98.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](O[C@@H]1C[C@H](C(=O)O)N(C(=O)OCc2ccccc2)C1)(c1ccccc1)c1ccccc1
Reaction #41709
(2R,4R)-4-(tert-butyl-diphenyl-silanyloxy)-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OCC=CCO)(c1ccccc1)c1ccccc1
Reaction #44493
4-(tert-Butyl-diphenyl-silanyloxy)-but-2-en-1-ol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OC1CCC=CCC1)(c1ccccc1)c1ccccc1
Reaction #44504
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)[C@H](NC(=O)OC(C)(C)C)c1cc(F)c(F)c(F)c1
Reaction #44607
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)[C@H](NC(=O)OC(C)(C)C)c1cc(F)c(F)c(F)c1
Reaction #44635
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNCCO[Si](c1ccccc1)(c1ccccc1)C(C)(C)C
Reaction #45665
compound
収率 39.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OC(CC#N)c1ccncc1)(c1ccccc1)c1ccccc1
Reaction #46677
3-(t-butyldiphenylsiloxy)-3-(4-pyridyl)propionitrile
収率 98.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OCc1cncc(Br)c1)(c1ccccc1)c1ccccc1
Reaction #49843
product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OCc1cncc(Br)c1)(c1ccccc1)c1ccccc1
Reaction #50184
product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OCc1cccc(C=O)c1)(c1ccccc1)c1ccccc1
Reaction #50880
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCO[C@H]1[C@@H](O)[C@H](n2cnc3c(NC(=O)c4ccccc4)ncnc32)O[C@@H]1CO[Si](c1ccccc1)(c1ccccc1)C(C)(C)C
Reaction #51521
title compound
収率 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OC[C@@H]1C[C@H](O)[C@@H](OCc2ccccc2)[C@H](n2c3cc(F)c(F)cc3c3c4c(c5c6cc(F)c(F)cc6[nH]c5c32)C(=O)NC4=O)O1)(c1ccccc1)c1ccccc1
Reaction #52146
12-[4-deoxy-6-O-(tert-butyldiphenylsilyl)-2-O-benzyl-β-D-glucopyranosyl]-2,3,9,10-tetrafluoro-12,13-dihydro-5H-indolo[2,3-a]pyrrolo [3,4-c]carbazole-5,7(6H)-dione
収率 69.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)cc(OC)c1
Reaction #52983
3,5-dimethoxy-1-[(t-butyldiphenylsilyloxy)methyl]benzene
収率 87.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)cc(OC)c1
Reaction #52986
3,5-dimethoxybenzyl tert-butyldiphenylsilyl ether
収率 87.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](O)(c1ccccc1)c1ccccc1
Reaction #53626
TBDPSOH
収率 141.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CCCCO[Si](c1ccccc1)(c1ccccc1)C(C)(C)C
Reaction #58863
t-butylpent-4-ynyloxy diphenyl silane
収率 98.0%DOI: 10.6084/m9.figshare.5104873.v1
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