Stereoselective carbonyl reductions of chloro-substituted 8-oxabicyclo[3.2.1]oct-6-en-3-ones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference32 articles.
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2. 8-Oxabicyclo[3.2.1]oct-6-en-3-one: Anwendungen in der asymmetrischen Synthese polyoxygenierter Bausteine
3. Oxyallyls in synthesis: Preparation of tricyclic thromboxane A2 analogues
4. 8-oxabicyclo[3.2.1]oct-6-en-3-one as a module for the synthesis of β-alkoxy-δ-valerolactones relevant to natural products and drugs
5. Chelation-Controlled Reduction of α-Methylated 8-Oxabicyclo[3.2.1]oct-6-en-3-ones with Samarium Diiodide. Diastereoselective Preparation of Secondary Alcohols
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3. (1R,2R,3R,4S,5S)-3-Methyl-8-oxabicyclo[3.2.1]oct-6-ene-2,4-diyl diacetate;Acta Crystallographica Section E Structure Reports Online;2011-07-23
4. Oxidation and Reduction;Organic Reaction Mechanisms · 2006;2010-05-06
5. Orbital Phase Environments and Stereoselectivities;Orbitals in Chemistry;2009
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