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1296023

O=C1OCCC1N1CCCCC1=O
Reaction #55684
heavy syrup
Ausbeute 107.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(OC3CCOC3=O)cc2n1Cc1ccccc1
Reaction #68325
title compound
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncnc2c1c(-c1ccc(Oc3ccccc3)cc1)cn2C1CCOC1=O
Reaction #79774
2-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]-butyrolactone
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(C(C)=O)c1OC1CCOC1=O
Reaction #94863
α-[(6-acetyl-2-methoxycarbonylphenyl)oxy]-γ-butyrolactone
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OCCC1SCCCO
Reaction #174820
DOI: 10.1039/C8SC04228D
O=C1OCCC12Sc1cc(Cl)ccc1C2=O
Reaction #182799
DOI: 10.1039/C8SC04228D
O=C(O)c1ccccc1SC1CCOC1=O
Reaction #244538
DOI: 10.1039/C8SC04228D
O=C1OCCC1Oc1ccc(C(F)(F)F)cc1
Reaction #259317
DOI: 10.1039/C8SC04228D
Nc1ncnc2c1c(-c1ccc(Oc3ccccc3)cc1)cn2C1CCOC1=O
Reaction #270859
DOI: 10.1039/C8SC04228D
O=C1OCCC1C(O)C1CC2C=CC1C2
Reaction #272520
DOI: 10.1039/C8SC04228D
Cc1nc(N)nc2c1C(=NOC1CCOC1=O)NC(c1ccc(F)cc1Br)C2
Reaction #272786
DOI: 10.1039/C8SC04228D
COC(=O)c1cc(Cl)c(NC(C)=O)cc1OC1CCOC1=O
Reaction #289389
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCN(C2CCOC2=O)CC1
Reaction #299277
DOI: 10.1039/C8SC04228D
O=C1OCCC1Nc1cccc(F)c1
Reaction #312689
3-[(3-fluorophenyl)amino]-dihydrofuran-2(3H)-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OCCC1Nc1ccccc1
Reaction #348487
alpha-phenylamino-gamma-butyrolactone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccccc1NC1CCOC1=O
Reaction #349564
α-[(2-carboxyphenyl)amino]-γ-butyrolactone
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OCCC1Sc1ccc(CO)cc1
Reaction #374524
DOI: 10.1039/C8SC04228D
O=C1OCCC1Oc1ccc(F)cc1
Reaction #390140
DOI: 10.1039/C8SC04228D
O=C1OCCC1N1CCCCC1=O
Reaction #393387
DOI: 10.1039/C8SC04228D
O=C1OCCC1Oc1ccccc1[N+](=O)[O-]
Reaction #399798
DOI: 10.1039/C8SC04228D
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