About: Structure−Activity Relationship Studies of Illudins: AnaloguesPossessing a Spiro-cyclobutane Ring

Documentation

scienceplus.abes.fr version Bêta

scienceplus.abes.fr | explorer

À propos de : Structure−Activity Relationship Studies of Illudins: AnaloguesPossessing a Spiro-cyclobutane Ring Goto Sponge NotDistinct Permalink

Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_25/w
Subject	Article
Title	Structure−Activity Relationship Studies of Illudins: AnaloguesPossessing a Spiro-cyclobutane Ring
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_25/101021jo0346499/m/web http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_25/101021jo0346499/m/print
related by	http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_25/101021jo0346499/authorship/1 http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_25/101021jo0346499/authorship/2 http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_25/101021jo0346499/authorship/3
Author	Cong Qiang Kelner Michael J. McMorris Trevor C.
Abstract	Bicyclic and tricyclic analogues of anticancer sesquiterpene illudin S have been synthesized. Thesecontain a spiro-cyclobutane instead of spiro-cyclopropane structure. The cytotoxicity of the formeris less than that of the corresponding cyclopropane-containing compounds.
article type	research-article
is part of this journal	The Journal of Organic Chemistry

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata