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698155

CC(=O)S[C@@H]1CO[C@H](COC(N)=O)C1
Reaction #83042
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(O)C1C(=O)N2C(C(=O)[O-])=C(SC3COC(COC(N)=O)C3)C(C)C12.[Na+]
Reaction #83043
desired product
Выход 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)C1C(=O)N2C(C(=O)[O-])=C(SC3COC(COC(N)=O)C3)C(C)C12.[Na+]
Reaction #83044
desired product
Выход 55.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)C1C(=O)N2C(C(=O)OCOC(=O)C(C)(C)C)=C(SC3COC(COC(N)=O)C3)C(C)C12
Reaction #83113
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(NC(=O)OCC[Si](C)(C)C)c2ccccc2[C@@H](O)[C@H]1O
Reaction #92732
2-(trimethylsilyl)ethyl rac-[(1R,2S,3R)-2,3-dihydroxy-1-methyl-2,3-dihydro-1H-inden-1-yl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C=Cc2ccc(Cl)nn2)cc(OC)c1OC
Reaction #174450
DOI: 10.1039/C8SC04228D
CNC(=O)OC1CN(C(=O)N(C)C)CC1Oc1ccc(Cl)cc1
Reaction #182616
DOI: 10.1039/C8SC04228D
CC(=O)OC1C2CC(C)(OC(=O)N2)C(OC(C)=O)C1OC(C)=O
Reaction #182933
DOI: 10.1039/C8SC04228D
COC(C)COC(=O)Nc1ccc(C2=NNC(=O)CC2C)cc1
Reaction #187095
DOI: 10.1039/C8SC04228D
C=C1N(CCC)C(=O)OC12CCN(Cc1ccccc1)CC2
Reaction #209945
DOI: 10.1039/C8SC04228D
O=C(OCC1CNCCO1)N1CCN(c2ccc(F)cc2)CC1
Reaction #225122
DOI: 10.1039/C8SC04228D
CC(=O)OC1C2CC(CN=[N+]=[N-])(OC(=O)N2)C(OC(C)=O)C1OC(C)=O
Reaction #229878
DOI: 10.1039/C8SC04228D
CCC(O)C(C)C1OC1CC(C)(O)C=CC=C(C)C1OC(=O)CC(O)CCC(C)(O)C(OC(=O)N2CCN(C3CCCCCC3)CC2)C=CC1C
Reaction #245970
DOI: 10.1039/C8SC04228D
CC(O)(COC(=O)N1CCN(C(=O)OC(C)(C)C)CC1)Cn1cc([N+](=O)[O-])nc1Cl
Reaction #248337
DOI: 10.1039/C8SC04228D
CC1(COC(=O)N2CCc3cc(Cl)ccc32)Cn2cc([N+](=O)[O-])nc2O1
Reaction #258611
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCOC(COC(=O)N2CCN(c3ccccc3)CC2)C1
Reaction #259341
DOI: 10.1039/C8SC04228D
O=C(OCC1CCCCO1)n1ccnc1
Reaction #259880
DOI: 10.1039/C8SC04228D
C=C(C)C(=O)NC(=O)OC1CCC(O)(CCl)C(C2(C)OC2CC=C(C)C)C1OC
Reaction #262243
DOI: 10.1039/C8SC04228D
CC1(COC(=O)N2CCC(Oc3ccc(C(F)(F)F)cc3)CC2)Cn2cc([N+](=O)[O-])nc2O1
Reaction #264017
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #277859
DOI: 10.1039/C8SC04228D
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