Authors: A V Shaptov V A Raldugin Yu V Gatilov I Yu Bagryanskaya M M Shakirov
Publish Date: 1994/03/01
Volume: 30, Issue: 2, Pages: 229-237
Abstract
The structures and the stereochemistries of all the main products of the carbocyclization of 5βacetoxyisocembrol on its interaction with aqueous formic acid in chloroform have been established This reaction takes place more selectively than the cyclization of cembrene under the same conditions and is distinguished by the complete predominance in its last stage of the 15hydride shift from C15 to C4 over the splitting out of a proton from the C4methyl group
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