Lewis acid B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub> catalyzed the Diels–Alder reactions of multisubstituted open-chain dienes and α,β-enals to afford the desired products with high <i>exo</i>-selectivities are reported. The substituent effect of the dienes and dienophiles on the product’s stereoselectivity was thoroughly investigated, and it was found that most of the desired <i>exo</i>-Diels–Alder products could be obtained in good yields and with high <i>exo</i>-stereoselectivities
High cis (i.e., endo) diastereoselectivities are witnessed in heat-promoted intramolecular Diels-Ald...
High cis (i.e., endo) diastereoselectivities are witnessed in heat-promoted intramolecular Diels-Ald...
High cis (i.e., endo) diastereoselectivities are witnessed in heat-promoted intramolecular Diels-Ald...
An efficient and alternative synthesis of <i>exo</i>-imidazolidin-2-one dienes is described. A conde...
An efficient and alternative synthesis of <i>exo</i>-imidazolidin-2-one dienes is described. A conde...
The Diels-Alder reactions of a series of silyloxydienes and silylated dienes with acyclic alpha,beta...
The Diels-Alder reaction has proven to be an invaluable tool in the arsenal of the synthetic organic...
A Lewis-acid catalyzed intermolecular Diels–Alder reaction between multisubstituted acyclic dienes a...
The factors controlling the reactivity and exo/endo selectivity of Diels–Alder reactions of geminal ...
An important goal for synthetic organic chemists is the synthesis of the desired isomer of a target ...
It has been known that substituents have a significant effect on the reactivity and selectivity of t...
[GRAPHICS] A combined experimental and theoretical study of the Diels-Alder reactions between 2-trim...
The Diels-Alder reaction was discovered in 1928 and has become the most efficient and practical met...
*S Supporting Information ABSTRACT: The intramolecular Diels−Alder reactions of cycloalkenones and t...
Abstract: A variety of Lewis acid reagents were utilized for Diels-Alder, aldol, and ene reactions w...
High cis (i.e., endo) diastereoselectivities are witnessed in heat-promoted intramolecular Diels-Ald...
High cis (i.e., endo) diastereoselectivities are witnessed in heat-promoted intramolecular Diels-Ald...
High cis (i.e., endo) diastereoselectivities are witnessed in heat-promoted intramolecular Diels-Ald...
An efficient and alternative synthesis of <i>exo</i>-imidazolidin-2-one dienes is described. A conde...
An efficient and alternative synthesis of <i>exo</i>-imidazolidin-2-one dienes is described. A conde...
The Diels-Alder reactions of a series of silyloxydienes and silylated dienes with acyclic alpha,beta...
The Diels-Alder reaction has proven to be an invaluable tool in the arsenal of the synthetic organic...
A Lewis-acid catalyzed intermolecular Diels–Alder reaction between multisubstituted acyclic dienes a...
The factors controlling the reactivity and exo/endo selectivity of Diels–Alder reactions of geminal ...
An important goal for synthetic organic chemists is the synthesis of the desired isomer of a target ...
It has been known that substituents have a significant effect on the reactivity and selectivity of t...
[GRAPHICS] A combined experimental and theoretical study of the Diels-Alder reactions between 2-trim...
The Diels-Alder reaction was discovered in 1928 and has become the most efficient and practical met...
*S Supporting Information ABSTRACT: The intramolecular Diels−Alder reactions of cycloalkenones and t...
Abstract: A variety of Lewis acid reagents were utilized for Diels-Alder, aldol, and ene reactions w...
High cis (i.e., endo) diastereoselectivities are witnessed in heat-promoted intramolecular Diels-Ald...
High cis (i.e., endo) diastereoselectivities are witnessed in heat-promoted intramolecular Diels-Ald...
High cis (i.e., endo) diastereoselectivities are witnessed in heat-promoted intramolecular Diels-Ald...