About: Hetero-Diels–Alder reaction of 1,3-bis(trimethylsilyloxy)-1,3-butadienes with arylsulfonylcyanides. Synthesis and antimicrobial activity of 4-hydroxy-2-(arylsulfonyl)pyridines

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About: Hetero-Diels–Alder reaction of 1,3-bis(trimethylsilyloxy)-1,3-butadienes with arylsulfonylcyanides. Synthesis and antimicrobial activity of 4-hydroxy-2-(arylsulfonyl)pyridines Goto Sponge NotDistinct Permalink

An Entity of Type : schema:ScholarlyArticle, within Data Space : wasabi.inria.fr associated with source document(s)

Attributes	Values
type	Academic Article research paper schema:ScholarlyArticle
isDefinedBy	Covid-on-the-Web dataset
has title	Hetero-Diels–Alder reaction of 1,3-bis(trimethylsilyloxy)-1,3-butadienes with arylsulfonylcyanides. Synthesis and antimicrobial activity of 4-hydroxy-2-(arylsulfonyl)pyridines
Creator	Langer, Peter Fischer, Christine Hussain, Ibrar Lalk, Michael Lindequist, Ulrike Villinger, Alexander Arfan Yawer, Mirza
Source	Elsevier; Medline; PMC
abstract	Abstract Hetero-Diels–Alder reactions of 1,3-bis(silyloxy)-1,3-butadienes with arylsulfonylcyanides afforded a variety of 4-hydroxy-2-(arylsulfonyl)pyridines. Several derivatives show antimicrobial activity against Gram-positive bacteria.
has issue date	2008-12-01(xsd:dateTime)
bibo:doi	10.1016/j.bmc.2008.10.033
bibo:pmid	18990580
has license	els-covid
sha1sum (hex)	a055ce10127f2cdd2e4ef0f320b96fb41c8f7339
schema:url	https://doi.org/10.1016/j.bmc.2008.10.033
resource representing a document's title	Hetero-Diels–Alder reaction of 1,3-bis(trimethylsilyloxy)-1,3-butadienes with arylsulfonylcyanides. Synthesis and antimicrobial activity of 4-hydroxy-2-(arylsulfonyl)pyridines
has PubMed Central identifier	PMC7125755
has PubMed identifier	18990580
schema:publication	Bioorganic & Medicinal Chemistry
resource representing a document's body	covid:a055ce10127f2cdd2e4ef0f320b96fb41c8f7339#body_text
is schema:about of	named entity 'variety' named entity 'bis' named entity 'Synthesis' named entity 'HETERO-DIELS-ALDER REACTION' named entity 'BUTADIENES' named entity 'GRAM-POSITIVE BACTERIA' named entity 'BACTERIA.' named entity 'VARIETY' named entity 'BIS' named entity 'ANTIMICROBIAL ACTIVITY' named entity 'BUTADIENES' named entity 'HYDROXY' named entity 'ALDER' named entity 'HYDROXY' named entity 'ANTIMICROBIAL ACTIVITY' named entity 'REACTIONS' named entity 'SYNTHESIS' named entity 'BIS' named entity 'butadienes' named entity 'reaction' named entity 'antimicrobial' named entity 'Diels-Alder reactions' named entity 'antimicrobial activity' named entity 'pyridines' named entity 'Diels-Alder reaction' named entity 'antimicrobial activity' named entity 'Bacillus subtilis' named entity 'tetrazoles' named entity 'structure-activity relationships' named entity 'nitriles' named entity 'nitriles' named entity 'antimicrobial activity' named entity 'silyloxy' named entity 'pyridines' named entity 'trimethylsilyloxy' named entity 'inhibitory activity' named entity '1,3-butadiene' named entity 'pyridine' named entity 'silyloxy' named entity 'cyanide' named entity 'n-heptane' named entity 'Sf9' named entity 'antibiotic activity' named entity 'pyridines' named entity 'azides' named entity 'recombinant' named entity 'azides' named entity 'Gram-positive' named entity 'starting materials' named entity 'Pyridines' named entity 'chlorinated' named entity 'inhibitory activity' named entity 'alkenes' named entity 'aqueous' named entity 'dihydrofolate reductase' named entity 'Gram-negative' named entity 'anthracene' named entity 'X-ray crystal structure' named entity 'binding activity' named entity 'pyridine' named entity 'CB2 receptor' named entity 'alkynes' named entity 'related compounds' named entity 'trimethylsilyloxy' named entity 'nitriles' named entity 'Nitriles' named entity 'carbon dioxide' named entity 'trichloroacetonitrile' named entity 'silyl enol ether' named entity 'protease' named entity 'pyridine' named entity 'deuterated solvents' named entity 'Ampicillin' named entity 'reaction time' named entity 'cycloaddition'

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