Literature DB >> 24022946

The oxide anion accelerated retro-diels-alder reaction.

M E Bunnage1, K C Nicolaou.   

Abstract

The widespread application of the retro-Diels-Alder reaction in synthesis has been hampered by the high temperatures usually required to effect cycloreversion. The discovery of the anionic oxy-Cope reaction was followed by predictions that the accelerating effect of the oxide anion should also be observed with other pericyclic reactions. Recently, such predictions have been confirmed for the retro-Diels-Alder reaction, which often proceeds rapidly at room temperature by oxide anion rate acceleration. Such mild retro-Diels-Alder reactions have now been employed in the synthesis of a range of molecular targets, including temperature-sensitive enediynes.
Copyright © 1997 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Diels-Alder reactions; oxide anion; pericyclic reactions; retro reactions; synthetic methods

Year:  1997        PMID: 24022946     DOI: 10.1002/chem.19970030204

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  2 in total

1.  Conformation of coenzyme pyrroloquinoline quinone and role of Ca2+ in the catalytic mechanism of quinoprotein methanol dehydrogenase.

Authors:  Y J Zheng; T C Bruice
Journal:  Proc Natl Acad Sci U S A       Date:  1997-10-28       Impact factor: 11.205

2.  Alternative Access to Functionalized 2,8-Ethanonoradamantane Derivatives.

Authors:  Pelayo Camps; Tània Gómez; Ane Otermin; Mercè Font-Bardia
Journal:  Molecules       Date:  2017-05-31       Impact factor: 4.411

  2 in total

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