Issue 19, 1996
From the journal:

Chemical Communications

Generation of the furan analogue of ortho-quinodimethane by 1,4-elimination of 3-acetoxymethyl-2-tributylstannylmethylfuran

Guo-Bin Liu,   Hajime Mori  and  Shigeo Katsumura  

Abstract

2,3-Dimethylene-2,3-dihydrofuran is generated in situ by boron trifluoride induced 1,4-conjugative elimination of tributylstannylmethyl acetate and then trapped with dienophiles to give the corresponding Diels–Alder cycloadducts.

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Article information

DOI
https://doi.org/10.1039/CC9960002251
Article type
Paper

Chem. Commun., 1996, 2251-2252

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Generation of the furan analogue of ortho-quinodimethane by 1,4-elimination of 3-acetoxymethyl-2-tributylstannylmethylfuran

G. Liu, H. Mori and S. Katsumura, Chem. Commun., 1996, 2251 DOI: 10.1039/CC9960002251

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