بحث البنية الفرعية

1015297

CCNC(=O)[C@H]1O[C@@H](OC)[C@@H]2OC(C)(C)O[C@@H]21
Reaction #10539
title compound
المردود 94.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(NCC(c2ccccc2)c2ccccc2)c2ncn([C@@H]3O[C@H](C(=O)O)[C@H]4OC(C)(C)O[C@H]43)c2n1
Reaction #10565
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)[C@H]1O[C@@H](n2cnc3c(NCC(c4ccccc4)c4ccccc4)nc(C(=O)OCC)nc32)[C@@H]2OC(C)(C)O[C@@H]21
Reaction #10566
title compound
المردود 78.9%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(I)nc2c1ncn2[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H]1O
Reaction #44333
6.8
المردود 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COCCOc1ccccc1
Reaction #47098
product 440
المردود 82.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COC(C)COC
Reaction #47109
product 473
المردود 64.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCOCC(CO)OCC(=O)O
Reaction #64237
title compound
المردود 53.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)COCC(=O)OC
Reaction #65331
diglycolic acid dimethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C1COCC(=O)NC(COCc2ccccc2)CNCC(COCc2ccccc2)N1
Reaction #65332
5,9-Bis(benzyloxymethyl)-1-oxa-4,7,10-triazacyclododecane-3,11-dione
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1O[C@H](CO)[C@@H]1O
Reaction #83112
desired product
المردود 96.2%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](NC(=O)[C@H](C)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCSC)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(=O)O)NC(=O)CNC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(=O)N[C@@H]1O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[C@]3(C(=O)O)C[C@H](O)[C@@H](NC(C)=O)[C@H](C[C@H](O)[C@H](O)CO)O3)[C@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1NC(C)=O)C(=O)NCC(=O)NCC(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](C)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(N)=O.O=C([O-])c1ccccc1O
Reaction #90248
exendin-4 salicylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)COCCOc1ccc(N)cc1
Reaction #170992
43
المردود 71.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COC(C)COC
Reaction #188343
DOI: 10.1039/C8SC04228D
CCCNC(=O)COC1CCC2(CO2)C(C2(C)OC2CC=C(C)C)C1OC
Reaction #189611
DOI: 10.1039/C8SC04228D
CC1(C)OC2C(C(=O)NNC(=O)C(C)(C)C)OC(n3cnc4c(Cl)ncnc43)C2O1
Reaction #197237
DOI: 10.1039/C8SC04228D
CC1(C)OC2C(C(=O)O)OC(n3cnc4c(N)nc(I)nc43)C2O1
Reaction #199795
DOI: 10.1039/C8SC04228D
C#CC=CC=CC1OC(C)(C)OC1COCC(=O)O
Reaction #237514
DOI: 10.1039/C8SC04228D
COCCOCCOCCOCC(=O)O
Reaction #251150
DOI: 10.1039/C8SC04228D
CC(C)Nc1ncnc2c1ncn2C1OC(C(=O)O)C2OC(C)(C)OC21
Reaction #265299
DOI: 10.1039/C8SC04228D
COC(=O)C1OC(c2ccc(Cl)c(Cc3ncc(-c4ccco4)s3)c2)C(OCc2ccccc2)C(OCc2ccccc2)C1OCc1ccccc1
Reaction #279203
DOI: 10.1039/C8SC04228D
الصفحة 1التالي