Literature DB >> 15174848

Enamines from terminal epoxides and hindered lithium amides.

David M Hodgson1, Christopher D Bray, Nicholas D Kindon.   

Abstract

A new reactivity mode of lithium amides with epoxides leads to hindered enamines. The reaction of some of these enamines with unactivated primary and secondary alkyl halides is described, which expands the range of electrophiles that one can use in the synthesis of mono-alkylated aldehydes.

Entities:  

Year:  2004        PMID: 15174848     DOI: 10.1021/ja031770o

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  3 in total

1.  Copper(I)/TEMPO-catalyzed aerobic oxidation of primary alcohols to aldehydes with ambient air.

Authors:  Jessica M Hoover; Janelle E Steves; Shannon S Stahl
Journal:  Nat Protoc       Date:  2012-05-24       Impact factor: 13.491

2.  CO/CO and NO/NO coupling at a hidden frustrated Lewis pair template.

Authors:  Tongdao Wang; Long Wang; Constantin G Daniliuc; Kamil Samigullin; Matthias Wagner; Gerald Kehr; Gerhard Erker
Journal:  Chem Sci       Date:  2017-01-04       Impact factor: 9.825

3.  Alkenes from β-lithiooxyphosphonium ylides generated by trapping α-lithiated terminal epoxides with triphenylphosphine.

Authors:  David M Hodgson; Rosanne S D Persaud
Journal:  Beilstein J Org Chem       Date:  2012-11-07       Impact factor: 2.883

  3 in total

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