plugin {
	version {1}
	name {informaworld}
	url {http://www.informaworld.com/}
	blurb {}
	author {Richard Apodaca}
	email {rich_apodaca@yahoo.com}
	language {ruby}
	regexp {www.informaworld.com}
}


# No need to have our own linkout - the use DOIs exclusively.

test {http://www.informaworld.com/smpp/content?content=10.1080/00397910701354392} {
	formatted_url {DOI http://dx.doi.org/10.1080/00397910701354392}
	linkout {DOI {} 10.1080/00397910701354392 {} {}}
	doi {10.1080/00397910701354392}
	serial 0039-7911
	year 2007
	start_page 1949
	type JOUR
	end_page 1956
	issue 12
	volume 37
	title {Facile Synthesis of 4-Functionalized Cyclopentenones}
	journal {Synthetic Communications: An International Journal for Rapid Communication of Synthetic Organic Chemistry}
	publisher {Taylor & Francis}
	status ok
	abstract {1-8-Diazabicyclo[5.4.0]undec-7-ene(DBU)-catalyzed Michael addition of nitroalkanes to dicyclopentadienone (<b>1</b>) followed by flash vacuum pyrolysis (FVP) provided a high-yielding synthesis of extremely pure 4-nitroalkyl cyclopentenones (<b>3</b>). The optimized Nef reaction of the nitro adducts (<b>2</b>) provided 4-ketoalkyl cyclopentenones (<b>5</b>) in the similar way.}
	url {http://www.informaworld.com/10.1080/00397910701354392}
	author {Ghorai Sujit SK {Ghorai, Sujit Kumar}}
	author {Hazra Nirmal NK {Hazra, Nirmal Kumar}}
	author {Mal Dipakranjan D {Mal, Dipakranjan}}
}

test {http://www.informaworld.com/smpp/content~content=a779515458~db=all~order=page} {
	formatted_url {DOI http://dx.doi.org/10.1080/00397910701357296}
	linkout {DOI {} 10.1080/00397910701357296 {} {}}
	doi {10.1080/00397910701357296}
	serial 0039-7911
	year 2007
	start_page 2079
	type JOUR
	end_page 2089
	issue 12
	volume 37
	title {Nitration of Ethyl Carbamates of Phenylenediamines and Aniline}
	journal {Synthetic Communications: An International Journal for Rapid Communication of Synthetic Organic Chemistry}
	publisher {Taylor & Francis}
	status ok
	abstract {The methyl and ethyl carbamates of aniline and the diethyl dicarbamates of 1,2-, 1,3-, and 1,4-phenylenediamine were prepared. Nitration of the carbamates gave ring mono-, di-, or trinitro-derivatives in good yield.}
	url {http://www.informaworld.com/10.1080/00397910701357296}
	author {Davis Matthew MC {Davis, Matthew C.}}
}