sodium carbonate

CCn1ncc(C(=O)c2ccc3c(c2C)C(OC)CCS3(=O)=O)c1OC(=O)C1CCCCC1
Reaction #1162
4-methoxy-5-methyl-6-(5-cyclohexylcarbonyloxy-1-ethylpyrazol-4-yl)carbonylthiochroman-1,1-dioxide
المردود 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CS[C@@H]1CN(C(=O)c2ccccc2)C[C@H]1N
Reaction #1411
1-Benzoyl-trans-3-amino-4-methylthio-pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #1472
crude material
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc2cc(C3CC(C)(C)c4ccccc4C3O[Si](C)(C)C(C)(C)C)ccc2c1
Reaction #1473
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Oc1ccc(CCN(Cc2ccccc2)C[C@H](O)COc2ccc(OCc3ccccc3)cc2)cc1
Reaction #1637
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(NCC(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)O)OCC1c2ccccc2-c2ccccc21
Reaction #1844
Fmoc-Gly-Pro-Hyp
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=Cc1ccc(O)cn1
Reaction #1915
product
المردود 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C#CCOc1cc(-n2nc(CCC3CO3)[nH]c2=O)c(Cl)cc1Cl
Reaction #2058
title compound
المردود 95.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOP(=O)(CCCCCO)OCC
Reaction #2108
Diethyl 5-hydroxypentylphosphonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CC(Br)CCc1ccccc1
Reaction #2347
ethyl 4-benzyl-3-bromobutyrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1NS(=O)(=O)c1cccnc1
Reaction #2502
title compound
المردود 83.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(c1ccc(F)cc1)C1CCN(CCCl)CC1
Reaction #2555
title compound
المردود 92.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1NCCN1CCC(C(=O)c2ccc(F)cc2)CC1
Reaction #2557
title compound
المردود 66.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)S(=O)(=O)C1=CCC(=NO)C=C1
Reaction #2568
title compound
المردود 102.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=Cc1ccc(O)cc1.C=Cc1ccc(OC2CCCCO2)cc1
Reaction #2770
p-tetrahydropyranyloxystyrene p-hydroxystyrene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=Cc1ccccc1CC(C(=O)O)N1C(=O)c2ccccc2C1=O
Reaction #2807
title compound
المردود 60.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
c1cncc(-c2cccs2)c1
Reaction #2867
title compound
المردود 16.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #3010
glass
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCCCCCCCCCOc1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #3028
1-octadecyloxy-2,4-dinitrobenzene
المردود 79.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCCCCCCCCCN(CCCCCCCCCCCCCCCCCC)c1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #3029
N,N-dioctadecyl-2,4-dinitrobenzenamine
المردود 87.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
الصفحة 1التالي