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Clc1ccn(-c2ncccc2Cl)n1
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title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_07
Clc1ccn(-c2ncccc2Cl)n1
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DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_04
Clc1ccn(-c2ncccc2Cl)n1
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Clc1ccn(-c2ncccc2Cl)n1
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Clc1ccn(-c2ncccc2Cl)n1
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DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_06
Cc1cc(-n2ccc(Cl)n2)sc1C=O
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title compound
Выход 38.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01
CCc1nc2c(F)ccc(OCC(=O)OC)c2c(OC(F)F)c1Cc1ccc(-n2ccc(Cl)n2)cc1
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title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_05
Cc1c(Cc2ccc(-n3ccc(Cl)n3)cc2)c(OC(F)F)nc2c(Cl)ccc(OCC(=O)OC(C)(C)C)c12
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title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_05
CCc1nc2c(F)ccc(OCC(=O)OC)c2c(OC(F)F)c1Cc1ccc(-n2ccc(Cl)n2)cc1
Reaction #2031515
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_03
Cc1c(Cc2ccc(-n3ccc(Cl)n3)cc2)c(OC(F)F)nc2c(Cl)ccc(OCC(=O)OC(C)(C)C)c12
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DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_03
Clc1ccn(-c2ncccc2Cl)n1
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Clc1ccn(-c2ncccc2Cl)n1
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Clc1ccn(-c2ncccc2Cl)n1
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