Target Specific Tactics in Olefin Metathesis: Synthetic
Approach to cis-syn-cis-Triquinanes and -Propellanes
Version 2 2016-04-11, 17:54Version 2 2016-04-11, 17:54
Version 1 2016-04-06, 14:22Version 1 2016-04-06, 14:22
Posted on 2016-04-06 - 00:00
A concise
and simple synthetic approach to cis-syn-cis-triquinanes and -propellanes
has been demonstrated via olefin metathesis starting with exo-nadic anhydride. This approach involves a ring-opening
and ring-closing metathesis sequence of norbornene derivatives using
Grubb’s catalyst. Early-stage diallylation of norbornene derivatives
is demonstrated followed by ring-closing metathesis that delivers
propellanes exclusively. Surprisingly, ring-opening metathesis, late-stage
diallylation, followed by ring-closing metathesis delivers triquinane
as well as propellane derivatives.
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Kotha, Sambasivarao; Aswar, Vikas R. (2016). Target Specific Tactics in Olefin Metathesis: Synthetic
Approach to cis-syn-cis-Triquinanes and -Propellanes. ACS Publications. Collection. https://doi.org/10.1021/acs.orglett.6b00537