110516-39-7Relevant academic research and scientific papers
8-Aminobicyclo[3.2.1]octanes: Synthesis and anti-viral activity
Miller,Ullah,Welsh,Hall
, p. 7503 - 7507 (2001)
A series of 8-chlorobicyclo[3.2.1]oct-6-enes has been prepared from cyclohexenyl chlorides and simple alkynes via a one-step [3+2] cycloaddition methodology, and then converted into the corresponding bicyclic amines. Against influenza-A virus a number of
BICYCLOOCT-6-ENES via (3+2)CYCLOADDITION
Gray, Brian D.,McMillan, Catherine M.,Miller, J. Allen,Moore, Michael
, p. 235 - 238 (2007/10/02)
(3+2)Cycloaddition of alkynes to allyl cations, generated from 3-chlorocyclohexenes and zinc chloride, provides a simple and direct route to bicyclooct-6-enes.
