Поиск подструктуры

742454

CCOP(=O)(OCC)C(CCCCNC(=O)c1ccccc1)P(=O)(OCC)OCC

Reaction #2070

title compound

Выход 30.7%DOI: 10.6084/m9.figshare.5104873.v1

CCOP(=O)(OCC)C(CCCCNCc1ccccc1)P(=O)(OCC)OCC

Reaction #2071

title compound

Выход 45.8%DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)c1ccc(/C(=C/c2ccc3c(c2)C(c2ccc(C)cc2)=CCC3(C)C)CC(OC)OC)cc1

Reaction #2702

title compound

DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)c1ccc(/C(=C/c2ccc3c(c2)C(c2ccc(C)s2)=CCC3(C)C)CC(OC)OC)cc1

Reaction #2706

title compound

DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)c1ccc(-c2cccc3cc4c(cc23)C(c2ccc(C)nc2)=CCC4(C)C)cc1

Reaction #2709

Ethyl 4-[1-(6-methyl-pyrid-3-yl)-3,4-dihydro-4,4-dimethyl-anthracen-8-yl]-benzoate

DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)c1ccc(-c2ccc3cc4c(cc3c2)C(c2ccc(C)cc2)=CC(C)(C)O4)cc1

Reaction #2713

title compound

DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)c1ccc(-c2ccc3cc4c(cc3c2)C(c2ccc(C)s2)=CC(C)(C)O4)cc1

Reaction #2717

title compound

DOI: 10.6084/m9.figshare.5104873.v1

Reaction #2721

product E

DOI: 10.6084/m9.figshare.5104873.v1

CCOP(=O)(CO[C@H](CO)COn1cnc2c(N)ncnc21)OCC

Reaction #6363

(R)-9-[2-(diethoxyphosphorylmethoxy)-3-hydroxypropoxy]adenine

Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1

CCOP(=O)(Cc1ccc(NC(=S)Nc2cc(-c3cc4cc(F)c(F)cc4[nH]3)ccc2OC)cc1)OCC

Reaction #53792

product

DOI: 10.6084/m9.figshare.5104873.v1

CCOP1(=O)OCC(C)(C)c2cc(OS(C)(=O)=O)ccc2O1

Reaction #55916

desired product

Выход 44.6%DOI: 10.6084/m9.figshare.5104873.v1

CC(C)(C)OC(=O)Nc1cc(C=C(CC(=O)OCc2ccccc2)C(=O)OC(C)(C)C)ccn1

Reaction #58034

2-(2-tert-Butoxycarbonylamino-pyridin-4-ylmethylene)-succinic acid 4-benzyl ester 1-tert-butyl ester

Выход 55.0%DOI: 10.6084/m9.figshare.5104873.v1

CC(C)(C)OC(=O)N[C@H]1CC[C@H](C=C(CC(=O)OCc2ccccc2)C(=O)OC(C)(C)C)CC1

Reaction #58040

trans-2-(4-tert-Butoxycarbonylamino-cyclohexylmethylene)-succinic acid 4-benzyl ester 1-tert-butyl ester

Выход 40.6%DOI: 10.6084/m9.figshare.5104873.v1

—

Reaction #67563

oil

Выход 119.0%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #82694

diethyl (3-methoxy-isoxazol-5-yl)-methane phosphonate

Выход 56.1%DOI: 10.6084/m9.figshare.5104873.v1

$CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCC/C=C\CCCCCCCC.CCCCCCCC/C=C\CCCCCCCCOCC(C[N+](C)(C)C)OCCCCCCCC/C=C\CCCCCCCC.[Cl-]$

Reaction #82860

DOTMA DOPC

DOI: 10.6084/m9.figshare.5104873.v1

$CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCC/C=C\CCCCCCCC.CCCCCCCC/C=C\CCCCCCCCOCC(C[N+](C)(C)C)OCCCCCCCC/C=C\CCCCCCCC.[Cl-]$

Reaction #82861

DOTMA DOPC

DOI: 10.6084/m9.figshare.5104873.v1

$CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCC/C=C\CCCCCCCC.CCCCCCCCC=CCCCCCCCC(=O)OCC(COP(=O)(O)OCC(O)CO)OC(=O)CCCCCCCC=CCCCCCCCC$

Reaction #82862

DOPG DOPC

DOI: 10.6084/m9.figshare.5104873.v1

CC(C)=CCC/C(C)=C/CC/C(C)=C/CC(P(=O)(OC(C)C)OC(C)C)P(=O)(OC(C)C)OC(C)C

Reaction #83190

Tetraisopropyl (E,E)-farnesylmethylenebisphosphonate

Выход 60.9%DOI: 10.6084/m9.figshare.5104873.v1

COc1ccc(N(c2ccc(OC)cc2)c2ccc(N(c3ccc(OC)cc3)c3ccc(OCCCP(=O)(O)O)cc3)cc2)cc1

Reaction #172182

3-(4-((4-(bis(4-methoxyphenyl)amino)phenyl)(4-methoxyphenyl)amino)phenoxy)propylphosphonic acid

DOI: 10.6084/m9.figshare.5104873.v1

Страница 1Далее