Use of allene in 1,3-dipolar addition to a carbonyl ylide: Syntheses of 3-hydroxy-cis-nemorensic acid and nemorensic acid
1,3-Dipolar addition of allene to the carbonyl ylide derived from 6-diazoheptane-2,5-dione is the key step in syntheses of 3-hydroxy-cis- nemorensic acid and nemorensic acid.
Hoofdauteurs: | Hodgson, D, Le Strat, F |
---|---|
Formaat: | Journal article |
Taal: | English |
Gepubliceerd in: |
2004
|
Gelijkaardige items
-
Use of allene in 1,3-dipolar addition to a carbonyl ylide: syntheses of 3-hydroxy-cis-nemorensic acid and nemorensic acid.
door: Hodgson, D, et al.
Gepubliceerd in: (2004) -
Concise, stereoselective syntheses of cis-nemorensic acid and 4-hydroxy-cis-nemorensic acid via tandem carbonyl ylide formation-cycloaddition.
door: Hodgson, D, et al.
Gepubliceerd in: (2002) -
Stereocontrolled syntheses of the nemorensic acids using 6-diazoheptane-2,5-dione in carbonyl ylide cycloadditions.
door: Hodgson, D, et al.
Gepubliceerd in: (2004) -
The synthesis of (+)-nemorensic acid
door: Donohoe, T, et al.
Gepubliceerd in: (2000) -
Preparation of (+)-nemorensic acid and approaches to nemorensine using the partial reduction of electron deficient furans
door: Donohoe, T, et al.
Gepubliceerd in: (2002)