類似構造検索

340

COc1ccc(NC[C@@H](C)O[Si](C)(C)C(C)(C)C)cc1C#N
Reaction #402
収率 47.6%
COc1ccc(NC[C@@H](C)O[Si](C)(C)C(C)(C)C)cc1C#N
Reaction #403
収率 20.6%
COc1ccc(NC[C@@H](C)O[Si](C)(C)C(C)(C)C)cc1C#N
Reaction #404
収率 62.2%
C[C@H](CNc1ccc(OCc2ccccc2)c(F)c1)O[Si](C)(C)C(C)(C)C
Reaction #424
収率 68.3%
C[C@H](CNc1ccc(OCc2ccccc2)c(F)c1)O[Si](C)(C)C(C)(C)C
Reaction #425
収率 61.4%
C[C@H](CNc1ccc(OCc2ccccc2)c(F)c1)O[Si](C)(C)C(C)(C)C
Reaction #426
収率 0.0%
C[C@H](CNc1ccc(OCc2ccccc2)c(F)c1)O[Si](C)(C)C(C)(C)C
Reaction #427
収率 67.7%
C[C@H](CNc1ccc(OCc2ccccc2)c(F)c1)O[Si](C)(C)C(C)(C)C
Reaction #428
収率 68.6%
C[C@H](CNc1ccc(OCc2ccccc2)c(F)c1)O[Si](C)(C)C(C)(C)C
Reaction #429
収率 69.6%
C[C@H](CNc1ccc(OCc2ccccc2)c(F)c1)O[Si](C)(C)C(C)(C)C
Reaction #430
収率 64.8%
C[C@H](CNc1ccc(OCc2ccccc2)c(F)c1)O[Si](C)(C)C(C)(C)C
Reaction #431
収率 73.6%
C[C@H](CNc1ccc(OCc2ccccc2)c(F)c1)O[Si](C)(C)C(C)(C)C
Reaction #432
収率 72.9%
C[C@H](CNc1ccc(OCc2ccccc2)c(F)c1)O[Si](C)(C)C(C)(C)C
Reaction #433
収率 67.5%
C[C@H](CNc1ccc(OCc2ccccc2)cc1)O[Si](C)(C)C(C)(C)C
Reaction #434
収率 65.2%
C[C@H](CNc1ccc(OCc2ccccc2)cc1)O[Si](C)(C)C(C)(C)C
Reaction #435
収率 18.9%
C[C@H](CNc1ccc(-c2c(F)cccc2F)cc1)O[Si](C)(C)C(C)(C)C
Reaction #533
収率 59.4%
C[C@@H](CONC(=O)c1ccc(=O)n(C)c1Nc1ccc(Br)cc1F)O[Si](C)(C)C(C)(C)C
Reaction #44256
(S)-2-(4-Bromo-2-fluorophenylamino)-N-(2-(tert-butyldimethylsilyloxy)propoxy)-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CO)O[Si](C)(C)C(C)(C)C
Reaction #166178
title product
収率 97.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CON1C(=O)c2ccccc2C1=O)O[Si](C)(C)C(C)(C)C
Reaction #166179
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CON)O[Si](C)(C)C(C)(C)C
Reaction #166180
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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