Literature DB >> 11457340

Catalyst-based control of [2,3]- and [3,3]-rearrangement in alpha-diazoketone-derived propargyloxy enols.

G A Moniz1, J L Wood.   

Abstract

Entities:  

Year:  2001        PMID: 11457340     DOI: 10.1021/ja015727h

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


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  2 in total

1.  Cationic dirhodium carboxylate-catalyzed synthesis of dihydropyrimidones from propargyl ureas.

Authors:  Miao Yang; Shannon J Odelberg; Zongzhong Tong; Dean Y Li; Ryan E Looper
Journal:  Tetrahedron       Date:  2013-07-08       Impact factor: 2.457

2.  Scope and mechanistic analysis of the enantioselective synthesis of allenes by rhodium-catalyzed tandem ylide formation/[2,3]-sigmatropic rearrangement between donor/acceptor carbenoids and propargylic alcohols.

Authors:  Zhanjie Li; Vyacheslav Boyarskikh; Jørn H Hansen; Jochen Autschbach; Djamaladdin G Musaev; Huw M L Davies
Journal:  J Am Chem Soc       Date:  2012-09-11       Impact factor: 15.419

  2 in total

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