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  • Reaction of dimethoxycarbene-DMAD zwitterion with 1,2-diones and anhydrides: a novel synthesis of highly substituted dihydrofurans and spirodihydrofurans.

Reaction of dimethoxycarbene-DMAD zwitterion with 1,2-diones and anhydrides: a novel synthesis of highly substituted dihydrofurans and spirodihydrofurans.

The Journal of organic chemistry (2006-03-11)
Vijay Nair, Ani Deepthi, Manojkumar Poonoth, Bindu Santhamma, Sreekumar Vellalath, Beneesh Pattoorpady Babu, Resmi Mohan, Eringathodi Suresh
ABSTRACT

The zwitterion formed by the reaction of dimethoxycarbene and DMAD adds efficiently to one of the carbonyl groups of 1,2-dicarbonyl compounds and anhydrides to generate dihydrofurans and spirodihydrofurans in good yields. In many cases, the carbene inserts into the C-C bond of the dione to yield masked vicinal tricarbonyl systems.

MATERIALS
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Product Description

Sigma-Aldrich
Dimethyl acetylenedicarboxylate, 95%