Catalytic enantioselective intermolecular cycloadditions of a 2-diazo-3,6-diketoester-derived carbonyl ylide with alkyne and strained alkene dipolarophiles
Catalytic enantioselective tandem carbonyl ylide formation-cycloaddition reactions of tert-butyl 2-diazo-3,6-dioxoheptanoate 7 with alkyne and strained alkene dipolarophiles to afford the corresponding cycloadducts with up to 92% ee are described. © 2003 Elsevier Science Ltd. All rights reserved.
Main Authors: | Hodgson, D, Labande, A, Glen, R, Redgrave, A |
---|---|
Format: | Journal article |
Language: | English |
Published: |
2003
|
Similar Items
-
Catalytic enantioselective intermolecular cycloadditions of 2-diazo-3,6-diketoester-derived carbonyl ylides with alkene dipolarophiles.
by: Hodgson, D, et al.
Published: (2004) -
Extended scope of dirhodium(II)-catalysed enantioselective intramolecular 1,3-dipolar cycloadditions of carbonyl ylides with alkene and alkyne dipolarophiles
by: Hodgson, D, et al.
Published: (2003) -
One-pot cross-metathesis/tandem carbonyl ylide formation-intramolecular cycloaddition of an unsaturated 2-diazo-3,6-diketoester.
by: Hodgson, D, et al.
Published: (2006) -
Catalytic enantioselective tandem carbonyl ylide formation-intramolecular cycloaddition with unsaturated alpha-diazo-beta,epsilon-diketo sulfones
by: Hodgson, D, et al.
Published: (2009) -
Catalytic enantioselective [3 + 2]-cycloadditions of diazoketone-derived aryl-substituted carbonyl ylides.
by: Hodgson, D, et al.
Published: (2003)