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Efficient Stereoselective Synthesis of the Enantiomers of Highly Substituted Paraconic Acids

✍ Scribed by Martín, Tomás; Rodríguez, Carmen M.; Martín, Victor S.


Book ID
126904687
Publisher
American Chemical Society
Year
1996
Tongue
English
Weight
169 KB
Volume
61
Category
Article
ISSN
0022-3263

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📜 SIMILAR VOLUMES


ChemInform Abstract: Efficient Stereosel
✍ T. MARTIN; C. M. RODRIGUEZ; V. S. MARTIN 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 2 views

Efficient Stereoselective Synthesis of the Enantiomers of Highly Substituted Paraconic Acids. -A short and efficient route to an important class of bioactive compounds, i.e. protolichesterinic acid (VI), rocellaric acid (VIII) and dihydroprotolichesterinic acid (XII) is achieved starting from the c

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A mixture of zinc chZoride and triethylamine effects the condensation of ary2 aZdehydes and of ketones with succinc anhydride to give paraconic acids.