o-Thioquinones on [2.2]paracyclophanes: an example of totally stereocontrolled hetero Diels–Alder reactions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference32 articles.
1. The Preparation of Helical Cyclophanes Containing Five-membered Rings
2. Stereoselective synthesis of enantiopure condensed [2.2]paracyclophanes
3. Reactions of (S)-(+)-4-ethenyl[2.2]paracyclophane with heterocyclic quinones
4. Synthesis of enantiopure helical cyclophanes containing five-membered heterocyclic rings
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1. Helical-Shaped Bis-1,4-benzoxathiines through an Inverse-Electron-Demand Hetero-Diels-Alder Reaction ofortho-Thioquinones;European Journal of Organic Chemistry;2016-10-10
2. Recent Contributions to Hetero Diels-Alder Reactions;Current Organic Chemistry;2016-07-28
3. Synthesis of Bromo-Substituted 4-Hydroxy[2.2]paracyclophanes and [2.2]Paracyclophane-4,7-quinones as Versatile Chiral Building Blocks;European Journal of Organic Chemistry;2014-12-05
4. Stereoselective Synthesis of Dithia[3.3]cyclophaneS,S′-Dioxides with Planar and Central Chirality;European Journal of Organic Chemistry;2014-02-03
5. An Efficient Catalytic Method for Regioselective Sulfenylation of Electron-Rich Aza-Aromatics at Room Temperature;European Journal of Organic Chemistry;2012-11-19
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