A Convenient Preparation of 3-Substituted Furans: Synthesis of Perillene and Dendrolasin

D. K. Barma; Abhijit Kundu; Rachid Baati; Charles Mioskowski; J R Falck

doi:10.1021/ol025708s

A Convenient Preparation of 3-Substituted Furans: Synthesis of Perillene and Dendrolasin

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

Biochemistry

Research output: Contribution to journal › Article › peer-review

32 Scopus citations

Abstract

(Matrix Presented) R= alkyl, allyl, propargyl, aryl 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/TMSCI.

Original language	English (US)
Pages (from-to)	1387-1389
Number of pages	3
Journal	Organic Letters
Volume	4
Issue number	8
DOIs	https://doi.org/10.1021/ol025708s
State	Published - Apr 18 2002

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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abstract = "(Matrix Presented) R= alkyl, allyl, propargyl, aryl 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/TMSCI.",

author = "Barma, {D. K.} and Abhijit Kundu and Rachid Baati and Charles Mioskowski and Falck, {J R}",

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T2 - Synthesis of Perillene and Dendrolasin

AU - Barma, D. K.

AU - Kundu, Abhijit

AU - Baati, Rachid

AU - Mioskowski, Charles

AU - Falck, J R

PY - 2002/4/18

Y1 - 2002/4/18

N2 - (Matrix Presented) R= alkyl, allyl, propargyl, aryl 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/TMSCI.

AB - (Matrix Presented) R= alkyl, allyl, propargyl, aryl 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/TMSCI.

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A Convenient Preparation of 3-Substituted Furans: Synthesis of Perillene and Dendrolasin

Abstract

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