Nucleophilic benzoylation using lithiated methyl mandelate as a synthetic equivalent of the benzoyl carbanion. Oxidative decarboxylation of α-hydroxyacids-Reference-Cited by-同舟云学术

Nucleophilic benzoylation using lithiated methyl mandelate as a synthetic equivalent of the benzoyl carbanion. Oxidative decarboxylation of α-hydroxyacids

Published:2001-02 Issue:6 Volume:57 Page:1075-1081
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Blay Gonzalo,Fernández Isabel,Formentin Pilar,Monje Belén,Pedro José R,Ruiz Rafael

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference23 articles.

1. Generation and synthetic applications of 2-lithio-1,3-dithianes

2. Nucleophile Acylierung mit 2-Lithium-1,3-dithianen bzw. -1,3,5-trithianen1,2,3

3. Synthesis of 17-(isocyanotosylmethylene) steroids: Precursors to pregnane derivatives

4. A new synthesis of α,β-unsaturated ketones. Allylic alkylation of 1-isocyano-1-tosylalkenes

5. Regioselective intramolecular base-Induced synthesis of .alpha.,.beta.-Unsaturated. Acyldecalins from Decalones via Carbon Homologation with isocyanomethyl Tosylate (TosMIC). Synthesis of (.+-.)-6-Eudesmen-4.alpha.-ol and (.+-.)-Vetiselinene

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