About: Efficient Access to 2-Isobetulinic Acid, 2-Isooleanolic Acid, and 2-Isoursolic Acid

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_18/w
Subject	Note
Title	Efficient Access to 2-Isobetulinic Acid, 2-Isooleanolic Acid, and 2-Isoursolic Acid
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_18/101021jo801232s/m/web http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_18/101021jo801232s/m/print
related by	http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_18/101021jo801232s/authorship/1 http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_18/101021jo801232s/authorship/2 http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_18/101021jo801232s/authorship/3 http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_18/101021jo801232s/authorship/4
Author	Wen Xiaoan Hao Jia Zhang Pu Sun Hongbin
Abstract	An efficient access to 2-isobetulin, 2-isobetulinic acid, 2-isooleanolic acid, and 2-isoursolic acid has been developed. The key step is a novel one-pot conversion of 2,3-dihydroxy triterpenes to 3-deoxy-2-oxo triterpenes. This method provides a new access to 3-deoxy-2-substituted pentacyclic triterpenes as potential therapeutic agents against metabolic diseases, tumors, and HIV infection.
is part of this journal	The Journal of Organic Chemistry

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