Academic literature on the topic 'N-Alkoxyacrylamides'

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Journal articles on the topic "N-Alkoxyacrylamides"

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Corminboeuf, Olivier, and Philippe Renaud. "N-Alkoxyacrylamides as Substrates for Enantioselective Diels−Alder Reactions." Organic Letters 4, no. 10 (2002): 1735–38. http://dx.doi.org/10.1021/ol0257981.

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Corminboeuf, Olivier, and Philippe Renaud. "ChemInform Abstract: N-Alkoxyacrylamides as Substrates for Enantioselective Diels-Alder Reactions." ChemInform 33, no. 40 (2010): no. http://dx.doi.org/10.1002/chin.200240077.

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Champetter, Philippe, Omar Castillo-Aguilera, Catherine Taillier та ін. "N -Alkoxyacrylamides in Domino Reactions: Catalytic and Stereoselective Access to δ-Lactams". European Journal of Organic Chemistry 2019, № 47 (2019): 7703–10. http://dx.doi.org/10.1002/ejoc.201901528.

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Genty, Axelle, Ismail Alahyen, Marie-José Tranchant та ін. "Straightforward Access to Polyfunctionalized δ-Lactams via Domino Aza–Michael/Thia–Michael/Aldol Sequence". Molecules 30, № 10 (2025): 2154. https://doi.org/10.3390/molecules30102154.

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Domino reactions are powerful tools for the straightforward synthesis of complex molecules with a particular emphasis on functionalized azacycles. We report a contribution in this field, implemented via a new thia–Michael/aldol sequence between readily accessible N-alkoxyacrylamides and α,β-unsaturated carbonyls, for access to polysubstituted δ-lactams with acceptable-to-good yields and good selectivity. This method, initially developed in a two-component approach and characterized by the mildness of its reaction conditions, was shown to be compatible with various thiophenol derivatives and to
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Cheng, Wan-Shun, Yong-Bing Ke, Yang Chen та ін. "Construction of chiral γ-lactam scaffolds via asymmetric cascade [3+2] annulation of N-alkoxyacrylamides catalyzed by a chiral-at-metal rhodium complex". Organic Chemistry Frontiers, 2025. https://doi.org/10.1039/d5qo00276a.

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An efficient asymmetric cascade [3+2] annulation of N-alkoxyacrylamides with α,β-unsaturated 2-acyl imidazoles catalyzed by a chiral-at-metal rhodium complex has been developed. The enantioenriched γ-lactam derivatives bearing three contiguous tertiary stereocenters...
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Rao, Gunda Ananda, Ramani Gurubrahamam, and Kwunmin Chen. "Base‐Catalysed [4+2]‐Annulation Between 2‐Nitrobenzofurans and N‐Alkoxyacrylamides: Synthesis of [3,2‐b]Benzofuropyridinones." European Journal of Organic Chemistry, July 6, 2022. http://dx.doi.org/10.1002/ejoc.202200657.

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Dissertations / Theses on the topic "N-Alkoxyacrylamides"

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Genty, Axelle. "Synthèse stéréοsélective d’hétérοcycles azοtés par réactiοns mοnοtοpes dοminο". Electronic Thesis or Diss., Normandie, 2024. http://www.theses.fr/2024NORMLH30.

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Les hétérocycles azotés sont particulièrement présents en chimie médicinale et pharmaceutique. Les δ-lactames, en particulier, connaissent un essor croissant en raison de leur fort intérêt biologique et de leur utilisation en tant qu'intermédiaires réactionnels pour la synthèse de molécules d'intérêt. L’étude croissante de ces composés conduit à une recherche de nouvelles voies de synthèse pour accéder à ces motifs polyfonctionnalisés. Les réactions monotopes se distinguent comme une stratégie privilégiée, permettant, en une seule étape, la formation de multiples liaisons et centres stéréogène
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