Organocatalyzed Asymmetric Conjugate Addition of Cyclic β‐Keto Esters to (E)‐β‐Nitroacrylate Derivatives

Abstract: A diaminomethylenemalononitrile organocatalyst efficiently promoted the asymmetric conjugate addition of cyclic β‐keto esters to (E)‐β‐nitroacrylate derivatives, yielding the corresponding β‐nitro esters derivatives with excellent enantioselectivities (up to >99 % ee). This is the first successful example of highly stereoselective conjugate addition of cyclic β‐keto esters to (E)‐β‐nitroacrylate derivatives to obtain anti‐isomers.

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
Organocatalyzed Asymmetric Conjugate Addition of Cyclic β‐Keto Esters to (E)‐β‐Nitroacrylate Derivatives ; day:12 ; month:11 ; year:2024 ; extent:6
Chemistry ; (12.11.2024) (gesamt 6)

Creator
Matsushima, Yasuyuki
Iijima, Yoshiyuki
Tanabe, Chinatsu
Nakashima, Kosuke
Hirashima, Shin‐ichi
Miura, Tsuyoshi

DOI
10.1002/asia.202401029
URN
urn:nbn:de:101:1-2411131322155.787960069043
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
15.08.2025, 7:21 AM CEST

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Associated

  • Matsushima, Yasuyuki
  • Iijima, Yoshiyuki
  • Tanabe, Chinatsu
  • Nakashima, Kosuke
  • Hirashima, Shin‐ichi
  • Miura, Tsuyoshi

Other Objects (12)