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1247857

COc1ccc(/C=C\c2cc(OC)c(OC)c(OC)c2)cc1O
Reaction #8837
combretastatin A-4
DOI: 10.6084/m9.figshare.5104873.v1
NOCCNC(=O)OCc1ccccc1
Reaction #77158
title compound
収率 95.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(=N)N(OCCNC(=O)OCc1ccccc1)C(=O)OC(C)(C)C
Reaction #77159
title compound
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)OC(C)(C)C)C(=NOCCN)NC(=O)OC(C)(C)C
Reaction #77173
title compound
収率 50.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CNC(=O)OCc1ccccc1)ON1C(=O)CCC1=O
Reaction #159280
Z-Gly-OSu
収率 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@H](CCC(=O)O)NC(=O)CNC(=O)OCc1ccccc1
Reaction #159281
Z-Gly-Glu-OtBu
収率 101.4%DOI: 10.6084/m9.figshare.5104873.v1
COCC1CC(C(=O)OCc2ccc([N+](=O)[O-])cc2)(N2OCC(NC(=O)OCc3ccccc3)C2=O)OC1=O
Reaction #231606
DOI: 10.1039/C8SC04228D
CN(C(=O)OC(C)(C)C)C(=NOCCN)NC(=O)OC(C)(C)C
Reaction #238952
DOI: 10.1039/C8SC04228D
COC1CC(C(=O)OCc2ccc([N+](=O)[O-])cc2)(N2OCC(NC(=O)OCc3ccccc3)C2=O)OC1=O
Reaction #243924
DOI: 10.1039/C8SC04228D
COC(OC)c1cc(OC(C)=O)c2c(c1)N1CC3NC3C(OC(C)=O)(O1)C2COC(N)=O
Reaction #259005
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C#N)=NOC(=O)C1CCCN1C(=O)OCc1ccccc1
Reaction #274886
DOI: 10.1039/C8SC04228D
O=C(NC1CON(C2(C(=O)OCc3ccc([N+](=O)[O-])cc3)OC(=O)c3ccccc32)C1=O)OCc1ccccc1
Reaction #276844
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC(=N)N(OCCN)C(=O)OC(C)(C)C
Reaction #277541
DOI: 10.1039/C8SC04228D
O=C1CCC(C(=O)OCc2ccc([N+](=O)[O-])cc2)(N2OCC(NC(=O)OCc3ccccc3)C2=O)O1
Reaction #290357
DOI: 10.1039/C8SC04228D
CCC(NC(=O)OCc1ccccc1)c1nc2cccc(C)c2c(=O)n1-c1ccccc1
Reaction #308484
quinazolinone
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc2nc(C(CO)Nc3nc(N)nc4[nH]cnc34)n(-c3ccccc3)c(=O)c12
Reaction #308489
product 68
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OCC(Nc1ncnc2[nH]cnc12)c1nc2ccccc2c(=O)n1-c1ccccc1
Reaction #308492
2-[2-tert-butoxy-1-(9H-purin-6-ylamino)-ethyl]-3-phenyl-3H-quinazolin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(C(=O)OCc2ccc([N+](=O)[O-])cc2)(N2OC[C@@H](NC(=O)OCc3ccccc3)C2=O)O1
Reaction #319375
subject compound ( 8 )
収率 75.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(C(=O)OCc2ccc([N+](=O)[O-])cc2)(N2OC[C@@H](NC(=O)OCc3ccccc3)C2=O)O1
Reaction #319376
subject Compound ( 8 )
収率 24.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(C(=O)OCc2ccc([N+](=O)[O-])cc2)(N2OC[C@H](NC(=O)OCc3ccccc3)C2=O)O1
Reaction #319377
subject Compound ( 9 )
収率 29.0%DOI: 10.6084/m9.figshare.5104873.v1
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