بحث البنية الفرعية

CC1(NCCO1)C

CNc1ccc(Oc2ccnc(C(=O)NCCO)c2)cc1[N+](=O)[O-]
Reaction #41790
4-(4-Methylamino-3-nitro-phenoxy)-pyridine-2-carboxylic acid (2-hydroxy-ethyl)-amide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1[C@@H](CC=O)COC1(C)C
Reaction #47304
(S)-2,2-dimethyl-4-(2-oxo-ethyl)-oxazolidine-3-carboxylic acid t-butyl ester
المردود 201.4%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@H](C)C[C@H](NC(=O)OC(C)(C)C)C(=O)O
Reaction #47315
(2S,4R)-2-t-butoxycarbonylamino-4-ethoxy-pentanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1[C@H](CO)COC1(C)C
Reaction #47471
(R)-4-hydroxymethyl-2,2-dimethyl-oxazolidine-3-carboxylic acid t-butyl ester
المردود 93.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1[C@@H]([C@@H](O)[C@@H](N)Cc2cc(F)cc(F)c2)COC1(C)C
Reaction #48611
desired compound
المردود 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cc(F)cc(F)c1)[C@H](O)[C@H]1COC(C)(C)N1C(=O)OC(C)(C)C
Reaction #48612
desired compound
المردود 72.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cc(F)cc(F)c1)[C@H](OCc1ccccc1)[C@H]1COC(C)(C)N1C(=O)OC(C)(C)C
Reaction #48613
desired compound
المردود 85.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)N(Cc2ccccc2)Cc2ccccc2)COC1(C)C
Reaction #48699
desired compound
المردود 87.0%DOI: 10.6084/m9.figshare.5104873.v1
COP(=O)(CC(=O)[C@@H]1COC(C)(C)N1C(=O)OC(C)(C)C)OC
Reaction #50362
(S)-3-(tert-butoxycarbonyl)-4-(2-(dimethoxyphosphoryl)-1-oxo-ethyl)-2,2-dimethyloxazolidine
المردود 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=N)N(c2ccc(C#N)c(C(F)(F)F)c2)C(=S)N1CCO
Reaction #64218
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(COC2CC(C3OC(C)(C)N(C(C)=O)C3Cc3cc(F)cc(F)c3)N(C(=O)OC(C)(C)C)C2)cc1
Reaction #177824
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C(c2ccc(NC(=O)c3ccc(Cl)cc3)cc2)COC1(C)C
Reaction #179948
DOI: 10.1039/C8SC04228D
COC(=O)CC1COC(C)(C)N1C(=O)OC(C)(C)C
Reaction #180526
DOI: 10.1039/C8SC04228D
CC(=O)OC(C(=O)N1C(Cc2ccccc2)COC1(C)C)c1ccc(-c2ccc(-c3ccccc3)cc2)o1
Reaction #180612
DOI: 10.1039/C8SC04228D
CC(C)N(CC1COC(C)(C)N1C(=O)OC(C)(C)C)c1ccccc1
Reaction #187226
DOI: 10.1039/C8SC04228D
CCCCC(C)(C)C(=O)NCC1OC(C)(C)N(C(=O)OC(C)(C)C)C1CC(CO)C(C)C
Reaction #187816
DOI: 10.1039/C8SC04228D
CC1(C)OCC(Cc2ccccc2)N1C(=O)Cc1ccc(-c2ccc(-c3ccccc3)cc2)o1
Reaction #194660
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C(CC2CCCOC2)COC1(C)C
Reaction #201081
DOI: 10.1039/C8SC04228D
CC(CC(N)CO)Oc1ccc(Cl)cc1
Reaction #201457
DOI: 10.1039/C8SC04228D
C#CC(NC(=O)OC(C)(C)C)C(C)O
Reaction #203812
DOI: 10.1039/C8SC04228D
الصفحة 1التالي