Literature DB >> 20877829

Auto-tandem catalysis: facile synthesis of substituted alkylidenecyclohexanones by domino (4+2) cycloaddition-elimination reaction.

Kiyosei Takasu1, Toru Tanaka, Takumi Azuma, Yoshiji Takemoto.   

Abstract

A catalytic domino reaction producing substituted 2-alkylidenecyclohexanone from 3-oxymethyl-2-siloxy-1,3-butadienes, which can be prepared from Baylis-Hillman adducts, and α,β-unsaturated ketones is described. The process involves two mechanistically distinct reactions, (4+2) cycloaddition and elimination. Both of these reactions are catalyzed by Tf(2)NH.

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Year:  2010        PMID: 20877829     DOI: 10.1039/c0cc03336g

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Synthesis of silyloxy dienes by silylene transfer to divinyl ketones: application to the asymmetric synthesis of substituted cyclohexanes.

Authors:  Christian C Ventocilla; K A Woerpel
Journal:  J Org Chem       Date:  2012-03-16       Impact factor: 4.354

2.  Tetramethyleneethane Equivalents: Recursive Reagents for Serialized Cycloadditions.

Authors:  Paul A Wender; Matthew S Jeffreys; Andrew G Raub
Journal:  J Am Chem Soc       Date:  2015-05-29       Impact factor: 15.419

  2 in total

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