CONFIGURATION OF DIELS–ALDER ADDUCT OF FURAN AND ACETYLENE DICARBOXYLIC ACID-Reference-Cited by-同舟云学术

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CONFIGURATION OF DIELS–ALDER ADDUCT OF FURAN AND ACETYLENE DICARBOXYLIC ACID

Published:1966-06-01 Issue:11 Volume:44 Page:1239-1245
ISSN:0008-4042
Container-title:Canadian Journal of Chemistry
language:en
Short-container-title:Can. J. Chem.

Author:

Kallos J.,Deslongchamps P.

Abstract

The configuration of the Diels–Alder adduct (I) of furan and acetylene dicarboxylic acid was established by chemical and spectroscopic methods and found to be exo–exo (IIa).

Publisher

Canadian Science Publishing

Subject

Organic Chemistry,General Chemistry,Catalysis

Link

http://www.nrcresearchpress.com/doi/pdf/10.1139/v66-185

Cited by 28 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A density functional theory study of the reactions of furans with substituted alkynes to form oxanorbornadienes and subsequent [4 + 2] and [2 + 2 + 2] addition reactions;Journal of Physical Organic Chemistry;2021-08-28

2. Tetra-porphyrin molecular tweezers: two binding sites linked via a polycyclic scaffold and rotating phenyl diimide core;Organic & Biomolecular Chemistry;2016

3. Rapid domino [3+2] cycloaddition, [4+2] cycloreversion, ring-opening and aromatisation of a fused oxanorbornane substrate;Tetrahedron Letters;2015-05

4. Stereoselective Tandem Cascade Furan Cycloadditions;The Journal of Organic Chemistry;2013-11-20

5. The Reactions of Diazoacetic Esters with Alkenes, Alkynes, Heterocyclic and Aromatic Compounds;Organic Reactions;2011-03-15

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