بحث البنية الفرعية

3021

C[Si](C)(C)OCCN(CCO[Si](C)(C)C)S(=O)(=O)c1ccccc1
Reaction #2934
title compound
المردود 88.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1cc[c]([Bi]([c]2ccc(S(=O)(=O)N(CCO)CCO)cc2S(=O)(=O)N(CCO)CCO)[c]2ccc(S(=O)(=O)N(CCO)CCO)cc2S(=O)(=O)N(CCO)CCO)c(S(=O)(=O)N(CCO)CCO)c1)N(CCO)CCO
Reaction #2935
title compound
المردود 79.5%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1cc[c]([Bi]([c]2ccc(S(=O)(=O)N(CCO)CCO)cc2S(=O)(=O)N(CCO)CCO)[c]2ccc(S(=O)(=O)N(CCO)CCO)cc2S(=O)(=O)N(CCO)CCO)c(S(=O)(=O)N(CCO)CCO)c1)N(CCO)CCO
Reaction #2936
title compound
المردود 94.7%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
المردود 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
CC(C)(C)[Si](C)(C)OCC1CCC(CO[Si](C)(C)C(C)(C)C)N1c1nc(-c2ccc(N)cc2)nc(N2C3CCC2COC3)n1
Reaction #188285
DOI: 10.1039/C8SC04228D
CC(C)(C)[Si](C)(C)OCCN(CCO[Si](C)(C)C(C)(C)C)C(=O)CCl
Reaction #226523
DOI: 10.1039/C8SC04228D
CC(C)(C)[Si](C)(C)OCC1CCC(CO[Si](C)(C)C(C)(C)C)N1c1nc(-c2ccc(N)cc2)nc(N2CC3CCC(C2)O3)n1
Reaction #233801
DOI: 10.1039/C8SC04228D
C[Si](C)(C)OC(=O)C1CC(O[Si](C)(C)C)CN1C(=O)CBr
Reaction #235102
DOI: 10.1039/C8SC04228D
C[Si](C)(C)OC(=O)C1CC(O[Si](C)(C)C)CN1C(=O)CCl
Reaction #249536
DOI: 10.1039/C8SC04228D
CC(C)(C)[Si](C)(C)OCCN(CCO[Si](C)(C)C(C)(C)C)c1ccc(O)cc1
Reaction #266394
DOI: 10.1039/C8SC04228D
C[Si](C)(C)OC(=O)[C@@H]1C[C@@H](O[Si](C)(C)C)CN1C(=O)CCl
Reaction #307927
trimethylsilyl (2S,4R)—N-chloroacetyl-4-(trimethylsilyloxy)pyrrolidine-2-carboxylate
المردود 95.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H]1C[C@@H](O)CN1C(=O)CCl
Reaction #307928
(2S,4R)—N-(chloroacetyl)-4-hydroxypyrrolidine-2-carboxylic acid
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)OC(=O)[C@@H]1C[C@@H](O[Si](C)(C)C)CN1C(=O)CCl
Reaction #307929
trimethylsilyl (2S,4R)—N-chloroacetyl-4-(trimethylsilyloxy)pyrrolidine-2-carboxylate
المردود 96.1%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)OC(=O)[C@@H]1C[C@@H](O[Si](C)(C)C)CN1C(=O)CBr
Reaction #307930
trimethylsilyl (2S,4R)—N-(bromoacetyl)-4-(trimethylsilyloxy)pyrrolidine-2-carboxylate
المردود 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(NC(=O)Nc2ccc(Oc3ccncc3)cc2)n(-c2cccc(N(CCO)CCO)c2)n1
Reaction #309083
desired product
المردود 36.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OCCN(CCO[Si](C)(C)C(C)(C)C)C(=O)CCl
Reaction #314337
N,N-bis-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2-chloro-acetamide
المردود 87.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](C(=O)O)c1ccc(OCC(=O)N(CCO[Si](C)(C)C(C)(C)C)CCO[Si](C)(C)C(C)(C)C)cc1
Reaction #314338
(R)-[4-({bis-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-carbamoyl}-methoxy)-phenyl]-tert-butoxycarbonylamino-acetic acid
المردود 91.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](c1ccccc1)[C@H](NC(=O)[C@H](N)c1ccc(OCC(=O)N(CCO)CCO)cc1)c1nc2ccc(I)cc2[nH]1
Reaction #314339
(R)-2-amino-2-(4-{[bis-(2-hydroxy-ethyl)-carbamoyl]-methoxy}-phenyl)-N-[(1S,2S)-1-(6-iodo-1H-benzoimidazol-2-yl)-2-phenyl-propyl]-acetamide
المردود 93.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](c1ccccc1)[C@H](NC(=O)[C@H](N)c1ccc(OCC(=O)N(CCO[Si](C)(C)C)CCO[Si](C)(C)C)cc1)c1nc2ccc(I)cc2[nH]1
Reaction #314340
(R)-2-amino-2-(4-{[bis-(2-trimethylsilanyloxy-ethyl)-carbamoyl]-methoxy}-phenyl)-N-[(1S,2S)-1-(6-iodo-1H-benzoimidazol-2-yl)-2-phenyl-propyl]-acetamide
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي