First enantioselective organocatalytic addition of Nitromethylphenylsulfone to Enals. Enantioselective synthesis of Cyclohexenones Bearing 3 Contiguousstereogeniccenters
First enantioselective organocatalytic addition of Nitromethylphenylsulfone to Enals. Enantioselective synthesis of Cyclohexenones Bearing 3 Contiguousstereogeniccenters
A highly enantioselectiveorganocatalyticnitromethylphenylsulfone addition to aliphatic ?,?-??unsaturated aldehydes is reported. The reaction is catalyzed by simple and commercially available secondary amines, affording the cyclic compounds in moderate yields, good diastereoselectivities and excellent enantioselectivities.
cascade reaction, enantioselective, organocatalysis, asymmetric synthesis, secondary amine, cyclization
467-471
Rios, Ramon
609bedf2-e886-4d62-a676-a32b6f8c1441
Hybelbauerova, Simona
8d66945d-1980-44c2-8e68-daca83f1de2a
Csarova, Ivana
628c97bf-7c23-471a-83a3-5781732e060f
Vesely, Jan
1853ff19-a906-4321-bd69-f7e434176fc3
2013
Rios, Ramon
609bedf2-e886-4d62-a676-a32b6f8c1441
Hybelbauerova, Simona
8d66945d-1980-44c2-8e68-daca83f1de2a
Csarova, Ivana
628c97bf-7c23-471a-83a3-5781732e060f
Vesely, Jan
1853ff19-a906-4321-bd69-f7e434176fc3
Rios, Ramon, Hybelbauerova, Simona, Csarova, Ivana and Vesely, Jan
(2013)
First enantioselective organocatalytic addition of Nitromethylphenylsulfone to Enals. Enantioselective synthesis of Cyclohexenones Bearing 3 Contiguousstereogeniccenters.
Current Organic Synthesis, 10 (3), .
(doi:10.2174/1570179411310030008).
Abstract
A highly enantioselectiveorganocatalyticnitromethylphenylsulfone addition to aliphatic ?,?-??unsaturated aldehydes is reported. The reaction is catalyzed by simple and commercially available secondary amines, affording the cyclic compounds in moderate yields, good diastereoselectivities and excellent enantioselectivities.
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Published date: 2013
Keywords:
cascade reaction, enantioselective, organocatalysis, asymmetric synthesis, secondary amine, cyclization
Organisations:
Organic Chemistry: Synthesis, Catalysis and Flow
Identifiers
Local EPrints ID: 362229
URI: http://eprints.soton.ac.uk/id/eprint/362229
ISSN: 1570-1794
PURE UUID: b9b98d99-f84e-4dda-bcd5-d2a5e26537f4
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Date deposited: 18 Feb 2014 15:13
Last modified: 14 Mar 2024 16:01
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Contributors
Author:
Simona Hybelbauerova
Author:
Ivana Csarova
Author:
Jan Vesely
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