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1113686

CC(O)Cc1cc2c(cc1C(=NNc1ncccn1)c1ccc([N+](=O)[O-])cc1)OCO2
Reaction #53363
title compound
Rendimiento 64.0%DOI: 10.6084/m9.figshare.5104873.v1
C(=C1C=C(c2ccccc2)OC(c2ccccc2)=C1)C(=Cc1cc(-c2ccccc2)[o+]c2ccccc12)c1ccccc1.[O-][Cl+3]([O-])([O-])[O-]
Reaction #74690
4-[3-(2,6-Diphenyl-4H-pyran-4-ylidene)-2-phenylpropen-1-yl]flavylium perchlorate
DOI: 10.6084/m9.figshare.5104873.v1
C1=CC(=CC(=Cc2cc(-c3ccccc3)[o+]c3ccccc23)c2ccccc2)c2ccccc2O1.[O-][Cl+3]([O-])([O-])[O-]
Reaction #74691
4-[3-(4H-Benzopyran-4-ylidene)-2-phenylpropen-1-yl]flavylium perchlorate
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C=CC1=CCN2C3=CC=C(CNC(=O)OC(C)(C)C)[C+]=C3C(C)(C)C2=C1.[O-][Cl+3]([O-])([O-])[O-]
Reaction #164000
2-(tert-Butoxycarbonylamino-methyl)-8-(2-dimethylamino-vinyl)-10,10-dimethyl-10H-pyrido[1,2-a]indolylium perchlorate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCC1=CC=C2C(=[C+]1)C(C)(C)C1=CC(CC#N)=CCN21.[O-][Cl+3]([O-])([O-])[O-]
Reaction #164001
2-(tert-Butoxycarbonylamino-methyl)-8-cyanomethyl-10,10-dimethyl-10H-pyrido[1,2-a]indolylium perchlorate
DOI: 10.6084/m9.figshare.5104873.v1
C(=C1C=C(c2ccccc2)OC(c2ccccc2)=C1)C(=Cc1cc(-c2ccccc2)[o+]c2ccccc12)c1ccccc1.[O-][Cl+3]([O-])([O-])[O-]
Reaction #311885
4-[3-(2,6-Diphenyl-4H-pyran-4-ylidene)-2-phenylpropen-1-yl]flavylium perchlorate
DOI: 10.6084/m9.figshare.5104873.v1
C1=CC(=CC(=Cc2cc(-c3ccccc3)[o+]c3ccccc23)c2ccccc2)c2ccccc2O1.[O-][Cl+3]([O-])([O-])[O-]
Reaction #311886
4-[3-(4H-Benzopyran-4-ylidene)2-phenylpropen-1-yl]flavylium perchlorate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(OCC)c1nnc2n1-c1ccc(Cl)cc1C(c1ccccc1)=NC2.[O-][Cl+3]([O-])([O-])[O-]
Reaction #355212
6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-carboxaldehyde-diethylacetal perchlorate
DOI: 10.6084/m9.figshare.5104873.v1
CCOCCC(=O)C(CC(=O)[O-])(C[N+](C)(C)C)O[Cl+3]([O-])([O-])[O-]
Reaction #367764
3-ethoxypropionyl carnitine perchlorate
DOI: 10.6084/m9.figshare.5104873.v1
CN=C(c1ccc(OC)cc1)c1c(C)cc(CC(=O)OC)n1C.[O-][Cl+3]([O-])([O-])O
Reaction #458099
title compound
Rendimiento 70.1%DOI: 10.6084/m9.figshare.5104873.v1
CN=C(c1ccc(C)cc1)c1c(C)cc(CC(=O)OC)n1C.[O-][Cl+3]([O-])([O-])O
Reaction #458100
title compound
Rendimiento 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CN=C(c1ccccc1)c1c(C)cc(CC(=O)OC)n1C.[O-][Cl+3]([O-])([O-])O
Reaction #458101
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #458102
bright yellow solid
Rendimiento 69.0%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #458103
yellow solid
Rendimiento 65.0%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #458104
green solid
Rendimiento 30.0%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #458105
bright yellow solid
Rendimiento 64.0%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #458106
lime
Rendimiento 14.0%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #458107
red viscous oil
Rendimiento 77.0%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #458108
green solid
Rendimiento 38.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1cc(C)c(C(=O)c2ccc(Cl)cc2)n1C
Reaction #458111
title compound
Rendimiento 65.0%DOI: 10.6084/m9.figshare.5104873.v1
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