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.
Egile Nagusiak: | Hodgson, D, Le Strat, F |
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Formatua: | Journal article |
Hizkuntza: | English |
Argitaratua: |
2004
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Antzeko izenburuak
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Use of allene in 1,3-dipolar addition to a carbonyl ylide: syntheses of 3-hydroxy-cis-nemorensic acid and nemorensic acid.
nork: Hodgson, D, et al.
Argitaratua: (2004) -
Concise, stereoselective syntheses of cis-nemorensic acid and 4-hydroxy-cis-nemorensic acid via tandem carbonyl ylide formation-cycloaddition.
nork: Hodgson, D, et al.
Argitaratua: (2002) -
Stereocontrolled syntheses of the nemorensic acids using 6-diazoheptane-2,5-dione in carbonyl ylide cycloadditions.
nork: Hodgson, D, et al.
Argitaratua: (2004) -
The synthesis of (+)-nemorensic acid
nork: Donohoe, T, et al.
Argitaratua: (2000) -
Preparation of (+)-nemorensic acid and approaches to nemorensine using the partial reduction of electron deficient furans
nork: Donohoe, T, et al.
Argitaratua: (2002)