Mechanism and site selectivity in the Diels-Alder reaction between protoanemonin and butadiene. A theoretical study-Reference-Cited by-同舟云学术

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Mechanism and site selectivity in the Diels-Alder reaction between protoanemonin and butadiene. A theoretical study

Published:1991-03 Issue:6 Volume:56 Page:2190-2193
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Branchadell Vicenc,Orti Juan,Ortuno Rosa Maria,Oliva Antonio,Font Josep,Bertran Juan,Dannenberg J. J.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo00006a041

Cited by 23 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. Dramatic influence of the substitution of alkylidene-5H-furan-2-ones in Diels–Alder cycloadditions with o-quinonedimethide as diene partner: en route to the CDEF polycyclic ring system of lactonamycin;Organic & Biomolecular Chemistry;2012

2. Theoretical Study of the Mechanism of an Inverse-Demand Diels–Alder Reaction;Arabian Journal for Science and Engineering;2011-12-23

3. An efficient synthesis of highly optically active 4-substituted-2(5H)-furanones from chiral 3-bromo-2(5H)-furanone;Chinese Journal of Chemistry;2010-08-26

4. Facile synthesis of oxaspirobicyclic butenolides via a domino Michael addition/aldol reaction/γ-lactonization sequence;Tetrahedron;2010-05

5. Diels–Alder cycloaddition of o-quinonedimethides and alkylidene-5H-furan-2-ones: new and rapid access to lambertellol cores and arthrinone derivatives;Organic & Biomolecular Chemistry;2010

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