The total synthesis of fukiic acid, an HIV-1 integrase inhibitor
摘要:
A successful synthesis of fukiic acid is described in 7% overall yield (6 steps from veratraldehyde). rac-Fukiic acid was found to be a potent inhibitor of HIV-1 integrase but did not reveal any antiviral activity in the MT-4 cells assay. (C) 2008 Elsevier Masson SAS. All rights reserved.
The total synthesis of fukiic acid, an HIV-1 integrase inhibitor
摘要:
A successful synthesis of fukiic acid is described in 7% overall yield (6 steps from veratraldehyde). rac-Fukiic acid was found to be a potent inhibitor of HIV-1 integrase but did not reveal any antiviral activity in the MT-4 cells assay. (C) 2008 Elsevier Masson SAS. All rights reserved.
A successful synthesis of fukiic acid is described in 7% overall yield (6 steps from veratraldehyde). rac-Fukiic acid was found to be a potent inhibitor of HIV-1 integrase but did not reveal any antiviral activity in the MT-4 cells assay. (C) 2008 Elsevier Masson SAS. All rights reserved.