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CC(O)OCCN

OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@H]1O
Reaction #7438
Gal
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2OCC(C)(C)C(C(=O)NCCC(=O)O)O2)cc1
Reaction #40283
3-{[2-(4-Methoxy-phenyl)-5,5-dimethyl-[1,3]dioxane-4-carbonyl]-amino}-propionic acid
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cc(F)cc(F)c1)[C@H](O)[C@H]1CO[C@@H](OCCC(C)(C)C)CN1C(=O)OC(C)(C)C
Reaction #48615
title compound
Ausbeute 99.4%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(C(=O)OC(C)(C)C)[C@@H]([C@@H](O)[C@@H](N)Cc2cc(F)cc(F)c2)CO1
Reaction #48619
title compound
Ausbeute 70.2%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@H]1CN(C(=O)OC(C)(C)C)C([C@@H](O)[C@@H](N)Cc2cc(F)cc(F)c2)CO1
Reaction #48670
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1N[C@@H]([C@@H](OCc2ccccc2)[C@H](Cc2cc(F)cc(F)c2)N(Cc2ccccc2)Cc2ccccc2)CO[C@H]1OCC1(F)CCCCC1
Reaction #48708
title compound
Ausbeute 31.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1[C@H](OCC(C)(C)C)OC[C@H](C(O)C(N)Cc2cc(F)cc(OCc3ccccc3)c2)N1C(=O)OC(C)(C)C
Reaction #48721
desired compound
Ausbeute 77.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](OCC2(CF)CCCC2)OC[C@@H]1[C@@H](OCc1ccccc1)[C@H](Cc1cc(F)cc(F)c1)N(Cc1ccccc1)Cc1ccccc1
Reaction #48749
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CO[C@H]1CN(C(=O)OC(C)(C)C)[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)C2CCCC2)CO1
Reaction #48760
desired compound
Ausbeute 98.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccccc1-c1c2ccc(=O)cc-2oc2cc(O)ccc12
Reaction #54905
fluorescein
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1[C@@H](NC(=O)Cc2cccc3c2Cc2ccccc2-3)[C@H](CO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)O[C@@H]1n1cnc2c(Cl)ncnc21
Reaction #58428
7
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=NCC(F)(F)F)Nc1nc(CO)ns1
Reaction #63106
5-[2-(2,2,2-trifluoroethyl)guanidino]-3-hydroxymethyl-1,2,4-thiadiazole
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@H]1[C@@H](OCCCCCCCCC(=O)NN)O[C@H](CO)[C@H](O)[C@@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O
Reaction #64003
hydrazide
DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc2c(c1)c(/C=C/c1cnn(CCOC3CCCCO3)c1)nn2C1CCCCO1
Reaction #69792
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Oc1ccc2c(c1)c(/C=C/c1cnn(CCOC3CCCCO3)c1)nn2C1CCCCO1)c1c(Cl)cncc1Cl
Reaction #69793
5-((R)-1-(3,5-Dichloropyridin-4-yl)ethoxy)-1-(tetrahydro-2H-pyran-2-yl)-3-((E)-2-(1-(2-(tetrahydro-2H-pyran-2-yloxy)ethyl)-1H-pyrazol-4-yl)vinyl)-1H-indazole
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(CCN2CCC3(CC2)OCC(CN2CCOCC2)O3)cc1
Reaction #164519
2-(morpholin-4-yl)methyl-8-phenethyl-1,4-dioxa-8-azaspiro[4,5]decane
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1OC[C@@H](O)[C@H](CN(CCOc2ccc(CCCCNC(=N)NC(=O)c3nc(Cl)c(N)nc3N)cc2)C[C@@H]2O[C@H](C)OC[C@H]2O)O1
Reaction #168508
11
Ausbeute 73.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](COC1CCCCO1)n1cc(C(=O)c2cncc(Br)c2)c2cncnc21
Reaction #169332
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](COC1CCCCO1)n1cc(C(=O)c2cncc(N)c2)c2cncnc21
Reaction #169334
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](COC1CCCCO1)n1cc(C(=O)c2cncc(NC(=O)Cn3nc4ccccc4n3)c2)c2cncnc21
Reaction #169335
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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