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1204663

CCCCC(c1ccc(OC2CCCCO2)cc1)N(C(=O)CCc1ccccc1)c1ccc(OCCN2CCCC2)cc1
Reaction #188542
DOI: 10.1039/C8SC04228D
COc1cc(OC2CCCCO2)ccc1CN(C(=O)C1CCCCC1)c1ccc(OCCN2CCCC2)cc1
Reaction #194916
DOI: 10.1039/C8SC04228D
O=C(NCc1ccc(O)cc1)N1CCN(Cc2ccc3c(c2)OCO3)CC1
Reaction #204111
DOI: 10.1039/C8SC04228D
O=C(C1CCCCC1)N(Cc1ccc(OC2CCCCO2)cc1Cl)c1ccc(OCCN2CCCC2)cc1
Reaction #205432
DOI: 10.1039/C8SC04228D
Cc1cc(C)c(S(=O)(=O)N(c2ccc(OCCN3CCCC3)cc2)C(C)c2ccc(O)cc2)c(C)c1
Reaction #245643
DOI: 10.1039/C8SC04228D
COc1ccc(S(=O)(=O)N(Cc2ccc(O)cc2)c2ccc(OCCN3CCCC3)cc2)cc1
Reaction #255381
DOI: 10.1039/C8SC04228D
O=S(=O)(c1ccc(C(F)(F)F)cc1Cl)N(Cc1ccc(O)cc1)c1ccc(OCCN2CCCC2)cc1
Reaction #257623
DOI: 10.1039/C8SC04228D
CN[C@H](CC(C)C)C(=O)N[C@H]1C(=O)N[C@@H](CC(N)=O)C(=O)N[C@H]2C(=O)N[C@H]3C(=O)N[C@H](C(=O)N[C@H](C(=O)O)c4cc(O)cc(O)c4-c4cc3ccc4O)[C@H](O)c3ccc(c(Cl)c3)Oc3cc2cc(c3O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[C@H]2C[C@](C)(N)[C@H](O)[C@H](C)O2)Oc2ccc(cc2Cl)[C@H]1O
Reaction #340232
Vancomycin
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H]1[C@H](Oc2c3cc4cc2Oc2ccc(cc2Cl)[C@@H](O[C@@H]2O[C@@H](CO)[C@@H](O)[C@H](O)[C@@H]2NC(C)=O)[C@@H]2NC(=O)[C@H](NC(=O)[C@@H]4NC(=O)[C@H]4NC(=O)[C@@H](Cc5ccc(c(Cl)c5)O3)NC(=O)[C@H](N)c3ccc(O)c(c3)Oc3cc(O)cc4c3)c3ccc(O)c(c3)-c3c(O[C@H]4O[C@H](CO)[C@@H](O)[C@@H](O)[C@@H]4O)cc(O)cc3[C@@H](C(=O)O)NC2=O)O[C@@H](CO)[C@@H](O)[C@@H]1O
Reaction #343132
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CC(=O)N(Cc1ccc(OC2CCCCO2)cc1Cl)c1ccc(OCCN2CCCC2)cc1
Reaction #369374
DOI: 10.1039/C8SC04228D
NCc1ccc(OC2CCCCO2)cc1
Reaction #370990
DOI: 10.1039/C8SC04228D
Cc1cc(C)c(S(=O)(=O)N(Cc2ccc(O)c(C)c2)c2ccc(OCCN3CCCC3)cc2)c(C)c1
Reaction #373818
DOI: 10.1039/C8SC04228D
Clc1cc(OC2CCCCO2)ccc1CNc1ccc(I)cc1
Reaction #393140
DOI: 10.1039/C8SC04228D
O=C(C1CCCCC1)N(Cc1ccc(O)cc1)c1ccc(OCCN2CCCC2)cc1
Reaction #406425
DOI: 10.1039/C8SC04228D
Cl.O=C(N[C@@H]1CNCCC[C@H]1OC(=O)c1ccc(O)cc1)c1ccc(O)cc1
Reaction #456633
4-Hydroxy-benzoic acid (3R,4R)-3-(4-hydroxy-benzoylamino)-azepan-4-yl ester hydrochloride
Rendimiento 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CN[C@H](CC(C)C)C(=O)N[C@H]1C(=O)N[C@@H](CC(N)=O)C(=O)N[C@H]2C(=O)N[C@H]3C(=O)N[C@H](C(=O)N[C@H](C(=O)O)c4cc(O)cc(O)c4-c4cc3ccc4O)[C@H](O)c3ccc(c(Cl)c3)Oc3cc2cc(c3O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[C@H]2C[C@](C)(N)[C@H](O)[C@H](C)O2)Oc2ccc(cc2Cl)[C@H]1O
Reaction #479210
vancomycin
DOI: 10.6084/m9.figshare.5104873.v1
O=C[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
Reaction #552005
mannose
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(N2C(=O)[C@H](CC[C@H](O)c3ccc(F)cc3)[C@H]2c2ccc(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]3O)cc2)cc1
Reaction #687369
title compound ( 8b )
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)NCCCc1ccc(N2C(=O)[C@H](CC[C@H](O)c3ccc(F)cc3)[C@H]2c2ccc(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]3O)cc2)cc1
Reaction #687370
title compound ( 9b )
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1O[C@@H](Oc2ccc([C@@H]3[C@@H](CC[C@H](OC(C)=O)c4ccc(F)cc4)C(=O)N3c3ccc(C#CC=O)cc3)cc2)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #687371
title compound 10c
DOI: 10.6084/m9.figshare.5104873.v1
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