This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
ChemInform Abstract: Synthesis of Highly Functionalized Pyrrolidines as Tunable Templates for the Direct Access to (.+‐.)‐Coerulescine and the Tricyclic Core of Martinellines. Issue 31 (11th July 2013)
Record Type:
Journal Article
Title:
ChemInform Abstract: Synthesis of Highly Functionalized Pyrrolidines as Tunable Templates for the Direct Access to (.+‐.)‐Coerulescine and the Tricyclic Core of Martinellines. Issue 31 (11th July 2013)
Main Title:
ChemInform Abstract: Synthesis of Highly Functionalized Pyrrolidines as Tunable Templates for the Direct Access to (.+‐.)‐Coerulescine and the Tricyclic Core of Martinellines.
<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>A series of tetrasubstituted pyrrolidines is synthesized by an aza‐Michael induced ring‐closure tandem reaction of bromide (II) with Michael acceptors (I), (IV), and (VI).</p> </abstract>