Synergistic catalysis: enantioselective addition of alkylbenzoxazoles to enals
Synergistic catalysis: enantioselective addition of alkylbenzoxazoles to enals
A novel catalytic enantioselective methodology based on synergistic catalysis is reported. The strategy involves: 1)?the metal-Lewis-acid activation of alkylazaarenes, and 2)?the secondary-amine activation of enals. Consequently, highly functionalized chiral alkylazaarenes were obtained in good yields and with reasonable stereoselectivity
16853-16857
Meazza, Marta
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Ceban, Victor
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Pitak, Mateusz B.
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Coles, Simon J.
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Rios, Ramon
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15 December 2014
Meazza, Marta
c4665645-8c77-4cfd-aa02-6bcc3341c1aa
Ceban, Victor
2e53f2b7-42ff-4c26-96e9-ef75891af166
Pitak, Mateusz B.
eeb6a00f-2291-4376-830f-d30dfd607ed1
Coles, Simon J.
3116f58b-c30c-48cf-bdd5-397d1c1fecf8
Rios, Ramon
609bedf2-e886-4d62-a676-a32b6f8c1441
Meazza, Marta, Ceban, Victor, Pitak, Mateusz B., Coles, Simon J. and Rios, Ramon
(2014)
Synergistic catalysis: enantioselective addition of alkylbenzoxazoles to enals.
Chemistry - A European Journal, 20 (51), .
(doi:10.1002/chem.201404565).
Abstract
A novel catalytic enantioselective methodology based on synergistic catalysis is reported. The strategy involves: 1)?the metal-Lewis-acid activation of alkylazaarenes, and 2)?the secondary-amine activation of enals. Consequently, highly functionalized chiral alkylazaarenes were obtained in good yields and with reasonable stereoselectivity
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e-pub ahead of print date: 28 October 2014
Published date: 15 December 2014
Organisations:
Chemistry
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Local EPrints ID: 371765
URI: http://eprints.soton.ac.uk/id/eprint/371765
ISSN: 0947-6539
PURE UUID: f35d1e5c-7488-455e-9914-38d7c59fd1fb
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Date deposited: 09 Jun 2016 11:04
Last modified: 15 Mar 2024 03:01
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Contributors
Author:
Marta Meazza
Author:
Victor Ceban
Author:
Mateusz B. Pitak
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