Literature DB >> 16267589

Michael, Michael-aldol and Michael-Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives.

Steven V Ley1, Darren J Dixon, Richard T Guy, Félix Rodríguez, Tom D Sheppard.   

Abstract

Consecutive coupling reactions of butane-2,3-diacetal protected glycolic acid derivatives with Michael acceptors and aldehydes are reported. An enantiopure sample of this building block was used to kinetically resolve a chiral Michael acceptor present as a racemic mixture of enantiomers.

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Year:  2005        PMID: 16267589     DOI: 10.1039/b512410g

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  2 in total

1.  Divergent synthesis and chemical reactivity of bicyclic lactone fragments of complex rearranged spongian diterpenes.

Authors:  Martin J Schnermann; Christopher M Beaudry; Nathan E Genung; Stephen M Canham; Nicholas L Untiedt; Breanne D W Karanikolas; Christine Sütterlin; Larry E Overman
Journal:  J Am Chem Soc       Date:  2011-10-11       Impact factor: 15.419

2.  Golgi-modifying properties of macfarlandin E and the synthesis and evaluation of its 2,7-dioxabicyclo[3.2.1]octan-3-one core.

Authors:  Martin J Schnermann; Christopher M Beaudry; Anastasia V Egorova; Roman S Polishchuk; Christine Sütterlin; Larry E Overman
Journal:  Proc Natl Acad Sci U S A       Date:  2010-03-23       Impact factor: 11.205

  2 in total

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