Dephosphonylation of α-fully substituted β-keto phosphonates with LiAlH4; regioselective alkylation of ketones employing phosphonate as a temporary activating group
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
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3. Phosphororganische Verbindungen, XXXV. PO‐aktivierte Verbindungen als Olefinierungsreagentien
4. Synthetic Applications of Phosphoryl-Stabilized Anions
5. Synthetic Applications of Dealkoxycarbonylations of Malonate Esters, β-Keto Esters, α-Cyano Esters and Related Compounds in Dipolar Aprotic Media - Part II
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1. Synthetic and Computational Studies on RhIII-Catalyzed Redox-Neutral Cascade of Carbenoid Functionalization and Dephosphonylative Annulation;The Journal of Organic Chemistry;2021-05-12
2. 8.28 Reduction of SulfurCarbon Bonds and of Other Heteroatoms Bonded to Tetrahedral Carbon;Comprehensive Organic Synthesis II;2014
3. LiAlH4-Induced Reductive Dephosphonylation of α,α-Dialkyl Triethyl β-Phosphonyl Esters: Mechanistic Study and Synthetic Application;Synlett;2012-02-28
4. An Easy Approach for the Synthesis of N-Substituted Isoindolin-1-ones;Synthesis;2012-01-26
5. ChemInform Abstract: Dephosphonylation of α-Fully Substituted β-Keto Phosphonates with LiAlH4. Regioselective Alkylation of Ketones Employing Phosphonate as a Temporary Activating Group.;ChemInform;2010-08-03
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