Alkylation of lithiated dimethyl tartrate acetonide with unactivated alkyl halides and application to an asymmetric synthesis of the 2,8-dioxabicyclo[3.2.1]octane core of squalestatins/zaragozic acids
(R,R)-Dimethyl tartrate acetonide 7 in THF/HMPA undergoes deprotonation with LDA and reaction at −78 °C during 12–72 h with a range of alkyl halides, including non-activated substrates, to give single diastereomers (at the acetonide) of monoalkylated tartrates 17, 24, 33a–f, 38a,b, 41 of R,R-configu...
Κύριοι συγγραφείς: | Sintim, H, Al Mamari, H, Almohseni, H, Fegheh-Hassanpour, Y, Hodgson, D |
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Μορφή: | Journal article |
Έκδοση: |
Beilstein-Institut
2019
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Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
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Alkylation of lithiated dimethyl tartrate acetonide with unactivated alkyl halides and application to an asymmetric synthesis of the 2,8-dioxabicyclo[3.2.1]octane core of squalestatins/zaragozic acids
ανά: Herman O. Sintim, κ.ά.
Έκδοση: (2019-05-01) -
Synthetic studies toward the Zaragozic agios (squalestatins).
ανά: Villalonga-Barber, C, κ.ά.
Έκδοση: (2000) -
Alkene ozonolysis in the presence of diazo functionality: accessing an intermediate for squalestatin synthesis
ανά: Almohseni, HAA, κ.ά.
Έκδοση: (2019) -
Selectivity in the cycloadditions of carbonyl ylides with glyoxylates: an approach to the zaragozic acids-squalestatins
ανά: Hodgson, D, κ.ά.
Έκδοση: (2000) -
Alkyl-Alkyl Suzuki Cross-Coupling of Unactivated Secondary Alkyl Chlorides
ανά: Lu, Zhe, κ.ά.
Έκδοση: (2013)