Substructure Search

1396292

CCOC(=O)C(=NOCCOC(=O)c1ccccc1)C(C)=O
Reaction #55547
ethyl 2-(2-benzoyloxyethoxyimino)-3-oxobutyrate
Yield 92.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC[C@H]1O[C@@H](N=C=S)[C@H](OC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@@H]1O[C@H]1O[C@H](COC(=O)c2ccccc2)[C@@H](O[C@H]2O[C@H](COC(=O)c3ccccc3)[C@@H](OC(=O)c3ccccc3)[C@H](OC(=O)c3ccccc3)[C@H]2OC(=O)c2ccccc2)[C@H](OC(=O)c2ccccc2)[C@H]1OC(=O)c1ccccc1)c1ccccc1
Reaction #162040
white solid
Yield 64.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCC1OC(n2ccnc2[N+](=O)[O-])C(OC(=O)c2ccccc2)C1OC(=O)c1ccccc1)c1ccccc1
Reaction #176865
DOI: 10.1039/C8SC04228D
CC(C)c1cc([N+](=O)[O-])ccc1C(=O)OCCn1ccnc1C(C)C
Reaction #176875
DOI: 10.1039/C8SC04228D
CCOC(=O)C(=NOCCOC(=O)c1ccccc1)C(C)=O
Reaction #196236
DOI: 10.1039/C8SC04228D
O=C(OCCBr)c1cccc(Cl)c1
Reaction #224299
DOI: 10.1039/C8SC04228D
O=C(O)C(F)(F)F
Reaction #243041
DOI: 10.1039/C8SC04228D
O=C(OC(COCc1ccccc1)C(Br)COCc1ccccc1)c1ccccc1
Reaction #260570
DOI: 10.1039/C8SC04228D
O=C(OCCN1CCN(c2cccc(Cl)c2)CC1)c1cccc2c1Cc1ccccc1-2
Reaction #299758
DOI: 10.1039/C8SC04228D
CCCC(OC(=O)c1ccccc1)C(C#N)CC.CCCCCCc1ccc(-c2ccccc2)cc1
Reaction #312195
pure product
Yield 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)SCC(Cc1ccccc1)C(=O)Nc1cccc(C(=O)OCCO)c1
Reaction #335883
title compound
Yield 55.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCCBr)c1ccccc1
Reaction #335971
2-Bromoethyl Benzoate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCC[n+]1ccccc1)c1ccccc1.[Br-]
Reaction #335972
N-(2-Benzoyloxyethyl)pyridinium Bromide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=NOCCOC(=O)c1ccccc1)C(C)=O
Reaction #342926
ethyl 2-(2-benzoyloxyethoxyimino)-3-oxobutyrate
Yield 92.4%DOI: 10.6084/m9.figshare.5104873.v1
[Br-]
Reaction #369803
DOI: 10.1039/C8SC04228D
COc1ccc(C(=O)O)c(Cl)c1OCCBr
Reaction #401391
DOI: 10.1039/C8SC04228D
Nc1ncnc2c1ncn2CCO
Reaction #423239
9-(2-hydroxyethyl)adenine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O[C@@H](COCc1ccccc1)[C@H](Br)COCc1ccccc1)c1ccccc1
Reaction #521503
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCCBr)c1ccccc1
Reaction #580541
title compound
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1
N#C[C@@H]1O[C@H](COC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@H]1OC(=O)c1ccccc1
Reaction #631915
product
Yield 524.3%DOI: 10.6084/m9.figshare.5104873.v1
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