An easy access to ( S )‐ and ( R )‐hydroxycyclohexenone
Author:
Affiliation:
1. Institut für Organische Chemie der Universität Hannover, Schneiderberg 1 B, W‐3000 Hannover 1, F.R.G.
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19911240732
Reference6 articles.
1. Part 4 of a series on cyclopentadienes as chiral templates. – For part 3 see ref.6).
2. Synthesis of two useful, enantiomerically pure derivatives of (S)-4-hydroxy-2-cyclohexenone
3. Asymmetric synthesis of (R) and (S)-4-hydroxy-2-cyclohexenone and derivatives
4. Chiral Cyclopentadienes
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2. Cycloadditions II;Key Chiral Auxiliary Applications;2014
3. Synthetic Approaches to Enantiomerically Enriched 4-Hydroxycyclohex-2-en-1-one - A Key Chiral Building Block in Complex Natural Product Synthesis;Synthesis;2010-11-26
4. ChemInform Abstract: Cyclopentadienes as Chiral Templates. Part 4. An Easy Access to (S)- and (R)-Hydroxycyclohexenone.;ChemInform;2010-08-22
5. An Efficient Protocol for the Enantioselective Preparation of a Key Polyfunctionalized Cyclohexane. New Access to (R)- and (S)-4-Hydroxy-2-cyclohexenone and (R)- and (S)-trans-Cyclohex-2-ene-1,4-diol;The Journal of Organic Chemistry;2008-03-26
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