Oxidation of diazo compounds by dimethyl dioxirane: an extremely mild and efficient method for the preparation of labile α-oso-aldehydes-Reference-Cited by-同舟云学术

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Oxidation of diazo compounds by dimethyl dioxirane: an extremely mild and efficient method for the preparation of labile α-oso-aldehydes

Published:1991-10 Issue:43 Volume:32 Page:6215-6218
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Ihmels Heiko,Maggini Michele,Prato Maurizio,Scorrano Gianfranco

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference40 articles.

1. Structure of FK506, a novel immunosuppressant isolated from Streptomyces

2. The use of vicinal tricarbonyl derivatives in alkaloid synthesis

3. The chemistry of vicinal tricarbonyls. A stable vinyl tricarbonyl hydrate as a di- and trielectrophile

4. The chemistry of vicinal tricarbonyls. New routes to indolizidines

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1. Synthesis and Physical Properties of 2-Oxoaldehydes and 2-Oxoacids;Chemistry of 2-Oxoaldehydes and 2-Oxoacids;2022

2. Dimethyldioxirane (DDO);Encyclopedia of Reagents for Organic Synthesis;2021-02-03

3. A Catalytic Asymmetric Ene Reaction for Direct Preparation of α-Hydroxy 1,4-Diketones as Intermediates in Natural Product Synthesis;Synlett;2020-02-19

4. Reinvestigation of Atipamezole Synthesis and Preparation of New Analogs;Organic Preparations and Procedures International;2019-07-04

5. Furo[2,3-g]thieno[2,3-e]indole: Application of an Ynamide-Based Benzannulation Strategy to the Synthesis of a Tetracyclic Heteroaromatic Compound;Organic Letters;2018-09-26

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