Bifunctional Squaramide Catalysts with the Same Absolute Chirality for the Diastereodivergent Access to Densely Functionalised Cyclohexanes through Enantioselective Domino Reactions. Synthesis and Mechanistic Studies. Issue 17 (16th October 2014)

• Record Type: Journal Article
• Authors: Martínez, Jose I.; Villar, Laura; Uria, Uxue; Carrillo, Luisa; Reyes, Efraím; Vicario, Jose L.
• Is Part Of: Advanced synthesis & catalysis. Volume 356:Issue 17(2014)
• Page Start: 3627
• Page End: 3648
• Publication Date: 2014-10-16
• Subjects: Catalysis -- Periodicals; Organic compounds -- Synthesis -- Periodicals; Chemistry -- Periodicals; Chemistry, Technical -- Periodicals; Chemistry -- Periodicals; Catalysis -- Periodicals; Technology, Pharmaceutical -- Periodicals; 547.2
• DOI: 10.1002/adsc.201400502
• Languages: English
• ISSNs: 1615-4150

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>We have developed a procedure for the stereoselective and diastereodivergent synthesis of densely functionalised cyclohexanes containing four stereocentres through an asymmetric Michael‐initiated ring closure (MIRC) cascade reaction employing hydrogen‐bond catalysis, which is able to prepare adducts with different absolute configurations starting from the same starting materials. The overall process involves a highly diastereo‐ and enantioselective Michael/Henry cascade reaction between a wide range of nitroalkenes and α‐nitro‐δ‐oxo esters, allowing access to different diastereoisomers of the final adduct by introducing subtle changes in the general (<italic>R</italic>, <italic>R</italic>)‐configured bifunctional tertiary amine/squaramide catalyst structure. Moreover, this methodology is also amenable to a three‐component one‐pot procedure, leading to the formation of the same adducts with very good results directly from commercially available reagents, on a multigram scale, and employing a very low catalyst loading. Furthermore, a detailed experimental and computational study is described which shows the origin of the diastereodivergent behaviour of these structurally similar catalysts and the nature of the substrate–catalyst interaction.</p> <p> <boxed-text content-type="graphic" position="anchor" orientation="portrait"> <graphic position="anchor" mimetype="image" xlink:href="ark:/27927/pgh2cmqcdht" orientation="portrait" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" /> </boxed-text> </p> </abstract>