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ChemInform Abstract: Highly Diastereoselective Synthesis of Chiral Furans with a Quaternary Carbon Substituent at the 2‐Position Using 8‐Phenylmenthol as the Chiral Auxiliary. Issue 42 (14th October 2014)
Record Type:
Journal Article
Title:
ChemInform Abstract: Highly Diastereoselective Synthesis of Chiral Furans with a Quaternary Carbon Substituent at the 2‐Position Using 8‐Phenylmenthol as the Chiral Auxiliary. Issue 42 (14th October 2014)
Main Title:
ChemInform Abstract: Highly Diastereoselective Synthesis of Chiral Furans with a Quaternary Carbon Substituent at the 2‐Position Using 8‐Phenylmenthol as the Chiral Auxiliary.
<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>The reaction of cyclopentane and cyclohexane carboxylates with cis‐pentenals (II) proceeds in the presence of a fluorinated cosolvent to afford the corresponding furan products with high diastereoselectivity.</p> </abstract>