647854-53-3Relevant academic research and scientific papers
ANTIVIRAL HETEROCYCLIC COMPOUNDS
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, (2021/04/10)
The present invention discloses compounds of Formula (I), or pharmaceutically acceptable salts, esters, or prodrugs thereof: which inhibit Human Respiratory Syncytial Virus (HRSV) or Human Metapneumovirus (HMPV) inhibitors. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject suffering from HRSV or HMPV infection. The invention also relates to methods of treating an HRSV or HMPV infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention.
First enantioselective synthesis of methyl (+)-7-methoxyanodendroate, an antitubercular dihydrobenzofuran
Aumann, Kylee M.,Hungerford, Natasha L.,Coster, Mark J.
supporting information; experimental part, p. 6988 - 6990 (2012/02/13)
An enantioselective synthesis of methyl (+)-7-methoxyanodendroate was achieved utilising a Claisen rearrangement, a Grubbs cross-metathesis, and a Shi epoxidation-cyclisation sequence, confirming the absolute configuration assigned to the natural product.
N-HYDROXYAMIDE DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY
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Page 59, (2010/11/30)
Novel N-hydroxyamide derivatives are disclosed. These N-hydroxyamide derivatives inhibit UPD-3O-(R-3-hydroxymyristoyl)-N-acetylglucosamine deacetylase, an enzyme present in gram negative bacteria and are therefore useful as antimicrobials and antibiotics. Methods of synthesis and of use of the compounds are also disclosed.
