Highly diastereoselective synthesis of spiropyrazolones
Highly diastereoselective synthesis of spiropyrazolones
We report a highly diastereoselective synthesis of spiropyrazolones catalyzed by secondary amines. The reported Michael-Aldol cascade reaction affords the desired spiropyrazolones bearing four chiral centers as a single diastereomer in excellent yields.
8574-8582
Ceban, Victor
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Olomola, Temitope
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Meazza, Marta
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Rios Torres, Ramon
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13 May 2015
Ceban, Victor
2e53f2b7-42ff-4c26-96e9-ef75891af166
Olomola, Temitope
b8a12c4c-8918-4c14-ba61-805de794a764
Meazza, Marta
c4665645-8c77-4cfd-aa02-6bcc3341c1aa
Rios Torres, Ramon
609bedf2-e886-4d62-a676-a32b6f8c1441
Abstract
We report a highly diastereoselective synthesis of spiropyrazolones catalyzed by secondary amines. The reported Michael-Aldol cascade reaction affords the desired spiropyrazolones bearing four chiral centers as a single diastereomer in excellent yields.
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molecules-20-08574.pdf
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Accepted/In Press date: 11 May 2015
Published date: 13 May 2015
Organisations:
Organic Chemistry: Synthesis, Catalysis and Flow
Identifiers
Local EPrints ID: 395916
URI: http://eprints.soton.ac.uk/id/eprint/395916
PURE UUID: 3eaac727-77f3-4ac8-8cf5-bb6fa6041dcf
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Date deposited: 02 Jun 2016 08:33
Last modified: 15 Mar 2024 00:44
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Author:
Victor Ceban
Author:
Temitope Olomola
Author:
Marta Meazza
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