π-Facial stereoselectivity in the diels-alder reaction-III.1 an unsymmetrically birdcage-annulated cyclohexadiene
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
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1. Revealing the Origin of Π‐facial and Regioselectivity in the Diels‐Alder Reaction of Unsymmetrical, Cage‐annulated 1,3‐Cyclohexadiene with Ethyl Propiolate Dienophile: a DFT Study;ChemistrySelect;2020-11-16
2. A DFT investigation of Diels-Alder reaction of ethyl propiolate to the cage-annulated hexacyclo[7.5.2.01,6.06,13.08,12.010,14]hexadeca-2,4-diene-7,16-dione;Journal of the Serbian Chemical Society;2018
3. ChemInform Abstract: π-Facial Stereoselectivity in the Diels-Alder Reaction. Part 3. An Unsymmetrically Birdcage-Annulated Cyclohexadiene.;ChemInform;2010-08-21
4. Regio- and π-facial selective Lewis acid interceded Diels–Alder reactions of α-dienyl-β-lactams: an indepth analysis;Tetrahedron;2008-07
5. Face-selectivity in [4+2]-cycloadditions to novel polycyclic benzoquinones. Remarkable stereodirecting effects of a remote cyclopropane ring and an olefinic bond;Tetrahedron Letters;2003-04
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