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: β‐Hydroxy‐γ‐lactones as Nucleophiles in the Nicholas Reaction for the Synthesis of Oxepene Rings. Enantioselective Formal Synthesis of (‐)‐Isolaurepinnacin (I) and (+)‐Rogioloxepane A (II). Issue 35 (2nd September 2014)
Record Type:
Journal Article
Title:
ChemInform Abstract: β‐Hydroxy‐γ‐lactones as Nucleophiles in the Nicholas Reaction for the Synthesis of Oxepene Rings. Enantioselective Formal Synthesis of (‐)‐Isolaurepinnacin (I) and (+)‐Rogioloxepane A (II). Issue 35 (2nd September 2014)
Main Title:
ChemInform Abstract: β‐Hydroxy‐γ‐lactones as Nucleophiles in the Nicholas Reaction for the Synthesis of Oxepene Rings. Enantioselective Formal Synthesis of (‐)‐Isolaurepinnacin (I) and (+)‐Rogioloxepane A (II).
<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>The key steps consist of an intermolecular Nicholas reaction with a β‐hydroxy‐γ‐lactone as a nucleophile and a ring closing metathesis reaction.</p> </abstract>