The Use and Thermodynamic Origin of the Trityl Buttress Effect in Intramolecular Diels-Alder Cycloaddition Reactions

E-ISSN： 1875-6271|13|4|617-622

ISSN： 1570-1794

Source： Current Organic Synthesis, Vol.13, Iss.4, 2016-08, pp. : 617-622

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Intramolecular Diels-Alder Reactions Utilizing Aldehyde and Ketone Dienophiles, A Rare Cycloaddition Reaction

Mini-Reviews in Organic Chemistry, Vol. 12, Iss. 2, 2015-04 ,pp. : 149-161

Bentham Science Publishers

Access to resources Recommend Favorite

A DFT Study of the Regioselectivity in Intramolecular Diels-Alder Reactions with Formation of a Tricyclodecane Skeleton

Letters in Organic Chemistry, Vol. 8, Iss. 2, 2011-02 ,pp. : 125-131

Bentham Science Publishers

Access to resources Recommend Favorite

Diels-Alder Cycloaddition in Medicinal Chemistry

Current Organic Chemistry, Vol. 20, Iss. 22, 2016-08 ,pp. : 2358-2378

Bentham Science Publishers

Access to resources Recommend Favorite

Regio- and Diastereoselective Nitroso Diels-Alder Cycloaddition Reactions of 3-dienyl-2-azetidinones with Nitrosoarenes

Letters in Organic Chemistry, Vol. 9, Iss. 6, 2012-07 ,pp. : 411-421

Bentham Science Publishers

Access to resources Recommend Favorite

Regioselective Diels-Alder Reactions of 3-Vinylindoles with Quinones

Letters in Organic Chemistry, Vol. 1, Iss. 1, 2004-01 ,pp. : 20-22

Bentham Science Publishers

Access to resources Recommend Favorite