Literature DB >> 15469322

Mercuric triflate-catalyzed synthesis of 2-methylfurans from 1-alkyn-5-ones.

Hiroshi Imagawa1, Takahiro Kurisaki, Mugio Nishizawa.   

Abstract

[reaction: see text] 2-Methylfurans were prepared by an effective cyclization of 1-alkyn-5-ones in the presence of mercuric triflate as the catalyst under very mild reaction conditions with high catalytic turnover up to 100 times. Benzene, toluene, or dichloromethane was the solvent of choice.

Entities:  

Year:  2004        PMID: 15469322     DOI: 10.1021/ol048730p

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


  3 in total

1.  Toward palau'amine: Hg(OTf)2-catalyzed synthesis of the cyclopentane core.

Authors:  Kosuke Namba; Yukari Kaihara; Hirofumi Yamamoto; Hiroshi Imagawa; Keiji Tanino; Robert M Williams; Mugio Nishizawa
Journal:  Chemistry       Date:  2009-07-06       Impact factor: 5.236

Review 2.  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

3.  End game strategies towards the total synthesis of vibsanin E, 3-hydroxyvibsanin E, furanovibsanin A, and 3-O-methylfuranovibsanin A.

Authors:  Brett D Schwartz; Craig M Williams; Paul V Bernhardt
Journal:  Beilstein J Org Chem       Date:  2008-10-08       Impact factor: 2.883

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.