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1129861

C[Si](C)(C)CCOC(=O)N[C@H]1C[C@@H]2C[C@@H]2[C@H]1N1C(=O)c2ccccc2C1=O
Reaction #84687
title compound
Ausbeute 78.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC[C@H](NC(=O)OCc2ccccc2)[C@H](NC(=O)OCC[Si](C)(C)C)C1
Reaction #84697
title compound
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](CC1CCCCC1)[C@H](O)CN(Cc1ccc(C#N)cc1)C(=O)OCC[Si](C)(C)C
Reaction #340748
tert-butyl (2S,3R)-4-(N-(4-cyanobenzyl)-N-(2-(trimethylsilyl)ethoxycarbonyl)amino)-1-cyclohexyl-3-hydroxybutan-2-ylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOC(=O)ON1C(=O)CCC1=O
Reaction #408334
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC2(CC1)CC(NC(=O)OCC[Si](C)(C)C)c1cccc(Br)c12
Reaction #477337
(±)-tert-butyl 7-bromo-3-((2-(trimethylsilyl)ethoxy)carbonylamino)-2,3-dihydrospiro[indene-1,4′-piperidine]-1′-carboxylate
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CO)NC(=O)OCC[Si](C)(C)C
Reaction #500798
colorless liquid
Ausbeute 108.2%DOI: 10.6084/m9.figshare.5104873.v1
CN(C[C@H](CC1(F)CCCCC1)NC(=O)OC(C)(C)C)C(=O)OCC[Si](C)(C)C
Reaction #538943
(S)-2-(trimethylsilyl)ethyl 2-(t-butoxycarbonylamino)-3-(1-fluorocyclohexyl)propyl(methyl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)OCCCC1CCCCC1
Reaction #538948
3-cyclohexylpropyl-(ethyl)carbamate
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC([C@H](CC1CCCCC1)NC(=O)OC(C)(C)C)N(C)C(=O)OCC[Si](C)(C)C
Reaction #538953
(2S)-tert-butyl 1-cyclohexyl-3-(N-methyl-N-(2-(trimethylsilyl)ethoxycarbonyl)amino)pentan-2-ylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H]1CC[C@H](NC(=O)OCC[Si](C)(C)C)CC1
Reaction #557881
title compound
Ausbeute 98.2%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOC(=O)N1CCN(c2ccc([N+](=O)[O-])cc2Br)CC1
Reaction #629140
desired product
Ausbeute 96.1%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOC(=O)N1CCn2c(nnc2-c2cnccn2)C1
Reaction #663872
desired product
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOC(=O)N1C[C@H](NOCc2ccccc2)CC[C@H]1C(=O)O
Reaction #798184
title compound
Ausbeute 86.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(NC(=O)OCC[Si](C)(C)C)C(=O)O
Reaction #1049209
DOI: 10.1039/C8SC04228D
CC(C)[C@@H](NC(=O)OCC[Si](C)(C)C)C(=O)O
Reaction #1103341
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOC(=O)ON1C(=O)CCC1=O
Reaction #1256080
1-[2(Trimethylsilyl)ethoxycarbonyloxy]pyrrolidin-2,5-dione
DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOC(=O)N[C@@H](Cc1cc(I)c(Oc2cc(I)c(O)c(I)c2)c(I)c1)C(=O)O
Reaction #1256081
N-Trimethylsilylethoxycarbonylthyroxine
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C[C@H](CC1CCCCC1)NC(=O)OC(C)(C)C)C(=O)OCC[Si](C)(C)C
Reaction #1341405
(2S)-2-(tert-butoxycarbonylamino)-1-(N-butyl-N-(2-(trimethylsilyl)ethoxycarbonyl)amino)-3-cyclohexylpropane
Ausbeute 106.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C[C@H](CO)NC(=O)OC(C)(C)C)C(=O)OCC[Si](C)(C)C
Reaction #1341495
(2R)-2-(t-butoxycarbonylamino)-3-(N-methyl-N-(2-(trimethylsilyl)ethoxycarbonyl)amino)propan-1-ol
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(CN(C)C(=O)OCC[Si](C)(C)C)CC2(O)CCCCC2)cc1
Reaction #1341501
2-(trimethylsilyl)ethyl 3-(1-hydroxycyclohexyl)-2-(tosylamino)propylmethylcarbamate
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
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