Nucleophilic 1,2-additions to the carbonyl group of p-quinones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference58 articles.
1. Nucleophilic 1,2-addition to the carbonyl group of p-quinones and a new molecular rearrangement of a pentaoxyphosphorane
2. A Cyclic Saturated Pentaalkoxyphosphorane. Diketols Via Oxyphosphoranes
3. Communications- A New Carbon-Carbon Condensation Reaction Induced by Phosphite Esters. Formation of a 2:1 Adduct in the Reduction of Acenaphthenequinone with Trimethyl Phosphite
4. A new carbon-carbon condensation via cyclic oxyphosphoranes. Tartaric acids from α-ketoesters
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1. Stereochemical implications in the synthesis of 3,3′-spirocyclopropyl oxindoles from β-aryl/alkyl-substituted alkylidene oxindoles;Tetrahedron;2015-09
2. Reactions of α-Diketones and o-Quinones with Phosphorus Compounds;Chemical Reviews;2002-02-07
3. REACTION OF PHOSPHORUS PENTACHLORIDE WITH QUINONES;Phosphorus and Sulfur and the Related Elements;1988-09
4. Nucleophile aromatische substitution bei der alkoholyse von pentaoxyphosphoranen aus naphtho[2,1-b]furan-1,2-dion und trialkylphosphiten;Journal of Heterocyclic Chemistry;1974-10
5. References;Annual Reports on NMR Spectroscopy;1974
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