Studies towards a stereocontrolled synthesis of the tricarboxylate core of the zaragozic acids-squalestatins by a cycloaddition-rearrangement strategy

Studies towards a stereocontrolled synthesis of the tricarboxylate core of the zaragozic acids-squalestatins by a cycloaddition-rearrangement strategy

Reaction of diazoketodiester 11 with methyl glyoxylate in toluene in the presence of catalytic rhodium(II) acetate gives predominantly the 6,8- dioxabicyclo[3.2.1]octane 13. Acid-catalysed rearrangement of the corresponding alcohol 14 favours at equilibrium the 2,8- dioxabicyclo[3.2.1]octane skeleto...

Bibliográfalaš dieđut
Váldodahkkit:	Hodgson, D, Villalonga-Barber, C
Materiálatiipa:	Journal article
Giella:	English
Almmustuhtton:	2000

Geahča maid

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Synthetic and computational studies on the tricarboxylate core of 6,7-dideoxysqualestatin H5 involving a carbonyl ylide cycloaddition-rearrangement.
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Evolution of a cycloaddition-rearrangement approach to the squalestatins: a quarter-century odyssey
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Almmustuhtton: (2004)

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Almmustuhtton: (2019)

Catalytic enantioselective rearrangements and cycloadditions involving ylides from diazo compounds
Dahkki: Hodgson, D, et al.
Almmustuhtton: (2000)

Catalytic enantioselective rearrangements and cycloadditions involving ylides from diazo compounds
Dahkki: Hodgson, D, et al.
Almmustuhtton: (2001)

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Almmustuhtton: (1953)

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Almmustuhtton: (2017)

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Almmustuhtton: (2005)

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Stereocontrolled synthesis of plant growth regulators Abscisic acid and Xanthoxin
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Stereocontrolled spirocyclic bislactams derived from pyroglutamic acid
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Genetic Investigation of Tricarboxylic Acid Metabolism during the Plasmodium falciparum Life Cycle
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Metabolic control and regulation of the tricarboxylic acid cycle in photosynthetic and heterotrophic plant tissues.
Dahkki: Araújo, W, et al.
Almmustuhtton: (2012)

Development of asymmetric cycloaddition chemistry.
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Almmustuhtton: (2001)

Tandem intermolecular radical addition-rearrangement for azacycle synthesis
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Almmustuhtton: (2004)

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Almmustuhtton: (2015)

Stereocontrolled functionalization of allyl and homoallylamines.
Dahkki: Davies, S
Almmustuhtton: (2005)

New approaches to stereocontrolled glycosylation
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Almmustuhtton: (2011)

Studies on the interaction of the histone demethylase KDM5B with tricarboxylic acid cycle intermediates
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Almmustuhtton: (2017)

A STEREOCONTROLLED APPROACH TO 1-BETA-METHYLCARBAPENEM
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Almmustuhtton: (1995)

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Dahkki: Paterson, I, et al.
Almmustuhtton: (2012)

Synthesis of (-)-xialenon A by enantioselective alpha-deprotonation-rearrangement of a meso-epoxide
Dahkki: Hodgson, D, et al.
Almmustuhtton: (2003)

Synthesis of azabicyclic systems using nitrogen-directed radical rearrangements.
Dahkki: Hodgson, D, et al.
Almmustuhtton: (2007)

An enantioselective epoxide rearrangement - Claisen rearrangement approach to prostaglandins and (+)-iridomyrmecin
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Almmustuhtton: (1997)

Pb-207 NMR chemical shifts of aryllead tricarboxylates
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Almmustuhtton: (1998)

Carbon Sources Tune Antibiotic Susceptibility in Pseudomonas aeruginosa via Tricarboxylic Acid Cycle Control
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Prospects for stereocontrol in the reduction of aromatic compounds
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Almmustuhtton: (1996)