Literature DB >> 10990421

Use of optically active cyclic N,N-dialkyl aminals in asymmetric induction.

M E Jung1, A Huang.   

Abstract

[reaction: see text]Cyclization of the optically active ketone N,N-dialkyl aminals A affords the diastereomer B as the major product with diastereoselectivities ranging from nearly 1:1 to essentially 100:0 depending on the cyclization studied.

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Year:  2000        PMID: 10990421     DOI: 10.1021/ol0001517

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  4 in total

1.  Intramolecular [1 + 4 + 1] cycloaddition: establishment of the method.

Authors:  Douglass F Taber; Pengfei Guo; Na Guo
Journal:  J Am Chem Soc       Date:  2010-08-18       Impact factor: 15.419

2.  Convenient access to bicyclic and tricyclic diazenes.

Authors:  Douglass F Taber; Pengfei Guo
Journal:  J Org Chem       Date:  2008-12-05       Impact factor: 4.354

3.  2-(3,4-Di-meth-oxy-phen-yl)-1-pentyl-4,5-diphenyl-1H-imidazole.

Authors:  Shaaban K Mohamed; Mehmet Akkurt; Adel A Marzouk; Kuldip Singh; Mustafa R Albayati
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2013-11-27

4.  Synthesis of Propargylamines via Michael Addition Using Methyl Vinyl Ketone Derivatives, 1-Alkynes, and Secondary Amines Catalyzed by Copper (I) Halides.

Authors:  Bantu Udaykumar; Mariappan Periasamy
Journal:  ACS Omega       Date:  2019-12-02
  4 in total

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