<?xml version='1.0' encoding='utf-8'?>
<oai_dc:dc xmlns:dc='http://purl.org/dc/elements/1.1/' xmlns:oai_dc='http://www.openarchives.org/OAI/2.0/oai_dc/' xmlns:xsi='http://www.w3.org/2001/XMLSchema-instance' xsi:schemaLocation='http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd'>
<dc:creator>Kulciţki, V.N.</dc:creator>
<dc:creator>Sîrbu (Răducan), T..</dc:creator>
<dc:creator>Ungur, N.D.</dc:creator>
<dc:date>2011-01-03</dc:date>
<dc:description xml:lang='en'>A selective rearrangement of a epoxi-homodrimanic substrate is described. Using fluorosulfonic acid at
low temperature leads by ring contraction to a perhydrindanic structure. On the contrary, using boron trifluoride-
diethyl ether at r.t. selectively brings about angular methyl migration.
</dc:description>
<dc:source>Chemistry Journal of Moldova 6 (1) 110-112</dc:source>
<dc:subject>terpenoids</dc:subject>
<dc:subject>homodrimane</dc:subject>
<dc:subject>epoxide</dc:subject>
<dc:subject>rearrangement</dc:subject>
<dc:subject>hydrindane</dc:subject>
<dc:title>On the peculiarities of the ring contraction
reactions of homodrimanes via acid mediated epoxide rearrangement
</dc:title>
<dc:type>info:eu-repo/semantics/article</dc:type>
</oai_dc:dc>