Literature DB >> 11950369

A convenient preparation of 3-substituted furans: synthesis of perillene and dendrolasin.

D K Barma1, Abhijit Kundu, Rachid Baati, Charles Mioskowski, J R Falck.   

Abstract

A variety of 3-substituted furans, including the natural products perillene and dendrolasin, are obtained in good yield via reductive annulation of 1,1,1-trichloroethyl propargyl ethers using catalytic Cr(II) regenerated by Mn/TMSCl. [reaction: see text]

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Year:  2002        PMID： 11950369     DOI： 10.1021/ol025708s

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


  2 in total

Review 1.  Transition metal-mediated synthesis of monocyclic aromatic heterocycles.

Authors:  Anton V Gulevich; Alexander S Dudnik; Natalia Chernyak; Vladimir Gevorgyan
Journal:  Chem Rev       Date:  2013-01-10       Impact factor: 60.622

2.  Cascade synthesis of (E)-2-alkylidenecyclobutanols.

Authors:  J R Falck; Anish Bandyopadhyay; Narender Puli; Abhijit Kundu; L Manmohan Reddy; Deb K Barma; Anyu He; Hongming Zhang; Dhurke Kashinath; Rachid Baati
Journal:  Org Lett       Date:  2009-10-15       Impact factor: 6.005
  2 in total

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