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CCOCCl

CCOCn1c(=O)c2c(ncn2Cc2ccccc2)n(C)c1=O
Reaction #2092
7-Benzyl-1-ethoxymethyl-3-methylxanthine
DOI: 10.6084/m9.figshare.5104873.v1
C=CCN1CCCN(c2ccc(C(=O)Nc3cc(CCc4cc(OC)cc(OC)c4)n[nH]3)cc2)CC1
Reaction #45160
title compound
المردود 14.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CCc2cc(NC(=O)c3ccc(N4CCCN(C5CC5)CC4)cc3)[nH]n2)cc(OC)c1
Reaction #45163
title compound
المردود 33.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CCc2cc(NC(=O)c3ccc(N4CCCN(C(C)C)CC4)cc3)[nH]n2)cc(OC)c1
Reaction #45165
title compound
المردود 42.9%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCCN(c2ccc(C(=O)Nc3cc(CCc4cc(OC)cc(OC)c4)n[nH]3)cc2)CC1
Reaction #45172
title compound
المردود 25.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOCn1c(C(N)=O)c(OC(C)C)c2cc(OC)ccc21
Reaction #49878
1-ethoxymethyl-5-methoxy-3-(1-methylethoxy)-1H-indole-2-carboxamide
المردود 59.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOCOC(=O)c1c(I)cc(I)c(NC(C)=O)c1I
Reaction #56528
product
المردود 32.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOCC(O)c1cc2[nH]cnc2c(F)c1Nc1ccc(Br)cc1Cl
Reaction #60293
desired product
المردود 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN1C(=O)C2(c3ccc(N)cc3)CC(c3ccc(N)cc3)(C2)C1=O
Reaction #63362
1,5-di-(4-aminophenyl)-3-n-propyl-3-azabicyclo[3.1.1]heptane-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #64096
liquid
المردود 78.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOCOC(=O)c1ccc(B2OC(C)(C)C(C)(C)O2)cc1
Reaction #66305
ethoxymethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
المردود 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOCn1cccn1
Reaction #74607
title compound
المردود 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Cl-]
Reaction #74686
(Ethoxymethyl)triphenylphosphonium chloride
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc(C2C=C(C(F)(F)F)NC3=C2C(=O)CCC3)c1
Reaction #82739
title compound
المردود 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CNc1ccccc1C(=O)OCCCC1CCC(=O)CC1=O
Reaction #164454
6
DOI: 10.6084/m9.figshare.5104873.v1
CN[C@@H]1CCN(c2ccnc(Cl)c2)C1
Reaction #164483
desired product
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[CH2]OCC
Reaction #165395
title compound
المردود 66.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOCOC(=O)c1ccc(B2OC(C)(C)C(C)(C)O2)cc1
Reaction #175074
DOI: 10.1039/C8SC04228D
CCOCn1cnc(SC)n1
Reaction #175428
DOI: 10.1039/C8SC04228D
CCOCCOC(=O)C1=C(C)N(COCC)C(C)=C(C(=O)OCCOCC)C1c1cccc([N+](=O)[O-])c1
Reaction #196922
DOI: 10.1039/C8SC04228D
الصفحة 1التالي