Thermic Cope reaction of 2-azetidinone-tethered 1,5-dienes: synthesis of tetrahydroazocinones
Pedro Almendros, Cristina Aragoncillo, Gema Cabrero and 10 more
ARKIVOC · 2009
doi:10.3998/ark.5550190.0011.308 (opens in a new tab)
We email you when a new notice or a question about this paper appears.
Abstract
We report herein full details of the first example of a Cope rearrangement in which the C3-C4 bond of the -lactam nucleus is the central bond of the 1,5-hexadiene system, thus providing an easy and efficient entry to novel, and in some cases optically pure functionalized azocinones.
Abstract licence: CC BY
References1
1 more reference, whose wording the paper’s licence keeps private.
Reads
Read by people on this page
None yet.
Checked or read by AI through naulon
None yet.
A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.
Are you an author?
Is this your paper?
Claim it to add your note and be paid when agents cite it. Free.