Enantioselective addition of oxindoles to aliphatic ?,?-unsaturated aldehydes
Enantioselective addition of oxindoles to aliphatic ?,?-unsaturated aldehydes
A highly enantioselective organocatalytic oxindole addition to ?,?-unsaturated aldehydes is reported. The reaction is catalyzed by simple and commercially available chiral secondary amines, affording the corresponding adducts with good yields and with moderate diastereoselectivities.
6624-6626
Bravo, Natalia
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Mon, Ignasi
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Companyó, Xavier
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Alba, Andrea-Nekane
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Moyano, Albert
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Rios, Ramon
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2 December 2009
Bravo, Natalia
b4885173-6065-4fb7-accb-392f7d05735b
Mon, Ignasi
ff5cf142-3d1b-4bf1-bb71-745d2a4559bd
Companyó, Xavier
446791db-6e0a-40f9-9f20-3a8e8af9803c
Alba, Andrea-Nekane
e96df5c1-b984-45c5-9620-1d7f0cec8faf
Moyano, Albert
07f92405-40f4-4fc4-97b3-9bd5c9c14baa
Rios, Ramon
609bedf2-e886-4d62-a676-a32b6f8c1441
Bravo, Natalia, Mon, Ignasi, Companyó, Xavier, Alba, Andrea-Nekane, Moyano, Albert and Rios, Ramon
(2009)
Enantioselective addition of oxindoles to aliphatic ?,?-unsaturated aldehydes.
Tetrahedron Letters, 50 (48), .
(doi:10.1016/j.tetlet.2009.09.038).
Abstract
A highly enantioselective organocatalytic oxindole addition to ?,?-unsaturated aldehydes is reported. The reaction is catalyzed by simple and commercially available chiral secondary amines, affording the corresponding adducts with good yields and with moderate diastereoselectivities.
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Published date: 2 December 2009
Organisations:
Chemistry
Identifiers
Local EPrints ID: 347733
URI: http://eprints.soton.ac.uk/id/eprint/347733
ISSN: 0040-4039
PURE UUID: a9c63cd1-8cfb-48d7-9adf-15770a6af465
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Date deposited: 29 Jan 2013 13:48
Last modified: 14 Mar 2024 12:51
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Author:
Natalia Bravo
Author:
Ignasi Mon
Author:
Xavier Companyó
Author:
Andrea-Nekane Alba
Author:
Albert Moyano
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