Teilstruktursuche

459297

CON(C)C(=O)[C@H]1C[C@@H](O[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)CN1C(=O)OCc1ccccc1
Reaction #41710
benzyl (2R,4R)-4-(tert-butyl-diphenyl-silanyloxy)-2-(methoxy-methyl-carbamoyl)-pyrrolidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@]1(C(N)=O)C(C)[C@@H](O)CN1C(=O)OCc1ccccc1
Reaction #41711
benzyl (2R,4R)-4-hydroxy-2-methoxy-methyl-carbamoyl-pyrrolidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(OCc2ccc(Cl)cn2)ccn1-c1ccc(OCCN2CC[C@@H](O)C2)cc1
Reaction #43351
title compound
Ausbeute 50.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)O[C@H]1CCN(CCOc2ccc(-n3ccc(OCc4ccc(Cl)cn4)cc3=O)cc2)C1
Reaction #43353
title compound
Ausbeute 72.1%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(OCc2ccc(Cl)cn2)ccn1-c1ccc(OCCN2CC[C@H](O)C2)cc1
Reaction #43354
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C12CC1C=CCCCCCC(NC(=O)OC(C)(C)C)C(=O)N1CC(O[Si](C)(C)C(C)(C)C)CC1C(=O)N2
Reaction #46089
14-tert-butoxycarbonylamino-18-(tert-butyl-dimethyl-silanyloxy)-2,15-dioxo-3,16-diaza-tricyclo[14.3.0.04,6]nonadec-7-ene-4-carboxylic acid ethyl ester
Ausbeute 96.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCCCCC=CC2CC2(C(=O)O)NC(=O)C2CC(O[Si](C)(C)C(C)(C)C)CN2C1=O
Reaction #46090
14-tert-butoxycarbonylamino-18-(tert-butyl-dimethyl-silanyloxy)-2,15-dioxo-3,16-diaza-tricyclo[14.3.0.04,6]nonadec-7-ene-4-carboxylic acid
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@@H](O[Si](C)(C)C(C)(C)C)CN1C
Reaction #62374
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)O[C@@H]1CNC[C@H]1O[Si](C)(C)C(C)(C)C
Reaction #66274
(3R,4R)-3,4-bis(tert-butyldimethylsilyloxy)pyrrolidine
Ausbeute 99.6%DOI: 10.6084/m9.figshare.5104873.v1
NC1=Nc2cc(-c3ccc(C(=O)N4CCCC4)cc3)ccc2C=C(C(=O)N2C[C@@H](O)[C@H](O)C2)C1
Reaction #66275
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(C(=O)N3CC[C@@H](O[Si](C)(C)C(C)(C)C)C3)cc2)OC1(C)C
Reaction #66281
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)ccc2c3cnc(Nc4ccc(N5CC[C@@H](O[Si](C)(C)C(C)(C)C)C5)cn4)nc3n(C3CCCC3)c21
Reaction #166350
compound 276
Ausbeute 49.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)O[C@@H]1CCN(c2ccc(Nc3ncc4c5ccnc(F)c5n(C5CCCC5)c4n3)nc2)C1
Reaction #166352
compound 278
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)O[C@H]1CCN(c2ccc(Nc3ncc4c5ccnc(F)c5n(C5CCCC5)c4n3)nc2)C1
Reaction #166354
Compound 280
DOI: 10.6084/m9.figshare.5104873.v1
CC1C(O[Si](C)(C)C(C)(C)C)CC(=O)N1c1ccc(C#N)c(C(F)(F)F)c1
Reaction #180825
DOI: 10.1039/C8SC04228D
CC(C)(C)[Si](C)(C)OC1CCN(CC#CCN2CCCCC2)C1=O
Reaction #181968
DOI: 10.1039/C8SC04228D
CCC1C(O)CC(=O)N1c1ccc(C#N)c(OC)c1
Reaction #184660
DOI: 10.1039/C8SC04228D
COC(=O)C1CC(O[Si](C)(C)C(C)(C)C)CN1C
Reaction #197203
DOI: 10.1039/C8SC04228D
CC1NC(=O)CC1O[Si](C)(C)C(C)(C)C
Reaction #207614
DOI: 10.1039/C8SC04228D
CC(O)[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)CCN1C(=O)OC(C)(C)C
Reaction #219868
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter