Diastereoselective Pd‐catalyzed Decarboxylative (4+2) Cycloaddition Reactions of 4‐Vinylbenzoxazinanones and 2‐Nitro‐1,3‐enynes

Abstract: A formal palladium‐catalyzed decarboxylative (4+2) cycloaddition reaction between 4‐vinylbenzoxazinanones and 2‐nitro‐1,3‐enynes has been developed to produce highly valuable, densely functionalized tetrahydroquinolines in moderate to excellent yields with high diastereoselectivity under mild reaction conditions. The optimised protocol tolerates a range of substituted 2‐nitro‐1,3‐enynes, which represent an under‐utilized class of dipolarophile for transition‐metal catalyzed cycloadditions. The employed reaction methodology facilitates efficient cycloaddition with both N‐H‐ and N‐Ts‐4‐vinylbenzoxazinanone dipole precursors. The stereochemistry of the major and minor diastereomeric (4+2) cycloadducts was determined by single crystal X‐ray analyses. A mechanistic rationale for the high intrinsic diastereoselectivity and preliminary enantioselective experiments are also presented. The tetrahydroquinoline cycloadduct products feature numerous pendant functionalities, including a vinyl handle, an internal alkyne motif and a nitro functionality (which functions as a latent C‐3 nitrogen substituent) for further synthetic manipulations.

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

Bibliographic citation
Diastereoselective Pd‐catalyzed Decarboxylative (4+2) Cycloaddition Reactions of 4‐Vinylbenzoxazinanones and 2‐Nitro‐1,3‐enynes ; day:25 ; month:10 ; year:2023 ; extent:8
Chemistry - a European journal ; (25.10.2023) (gesamt 8)

Creator
Tague, Andrew J.
Hoang Pham, Quoc
Richardson, Christopher
Pyne, Stephen G.
Hyland, Christopher J. T.

DOI
10.1002/chem.202302406
URN
urn:nbn:de:101:1-2023102515491836611010
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
14.08.2025, 10:48 AM CEST

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Associated

  • Tague, Andrew J.
  • Hoang Pham, Quoc
  • Richardson, Christopher
  • Pyne, Stephen G.
  • Hyland, Christopher J. T.

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