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Papers by Darren Cundy
Journal of the Chemical Society, Perkin Transactions 1, 1999
Page 1. J. Chem. Soc., Perkin Trans. 1, 1999, 559567 559 An asymmetric synthesis of ADDA and ADD... more Page 1. J. Chem. Soc., Perkin Trans. 1, 1999, 559567 559 An asymmetric synthesis of ADDA and ADDA-glycine dipeptide using the β-lactam synthon method Darren J. Cundy,a Andrew C. Donohuea and Tom D. McCarthya,b*1 ...
A Convenient Large-Scale Preparation of endo-2-Methylbicyclo(2.2.1) hept-5-ene-exo-2-carboxylic A... more A Convenient Large-Scale Preparation of endo-2-Methylbicyclo(2.2.1) hept-5-ene-exo-2-carboxylic Acid.
Tetrahedron Letters, 1998
A range of NH substrates of varying nucleophilicity were reacted with a selection of electronical... more A range of NH substrates of varying nucleophilicity were reacted with a selection of electronically diverse aryl boronic acids in the presence of cupric acetate in order to evaluate the generality of a previously described N-arylation procedure. The results of that investigation are discussed.
Synthetic Communications, 1995
Synthetic Communications, 1993
The title anion readily reacts with a variety of electrophiles to give adducts which, upon treatm... more The title anion readily reacts with a variety of electrophiles to give adducts which, upon treatment with methanol in the presence of p-toluenesulfonic acid, afford the corresponding α-functionalized dimethyl acetals.
Organic Preparations and Procedures International, 1995
Bioorganic & Medicinal Chemistry Letters, 1997
Derivatives of 3- and 1-(4′-hydroxy-3′-(hydroxymethyl)butyl)-imidazo[4,5-b]pyridine were prepared... more Derivatives of 3- and 1-(4′-hydroxy-3′-(hydroxymethyl)butyl)-imidazo[4,5-b]pyridine were prepared in several steps from 2-amino-5-chloropyridine. Selected compounds were evaluated against human cytomeglovirus (HCMV), herpes simplex virusus (HSV1/HSV2) and varicella zoster virus (VZV). Details of their synthesis and biological activities are presented.
Bioorganic & Medicinal Chemistry Letters, 1995
A series of substituted 2,2′-bipyridine derivatives was prepared using the Kröhnke reaction and a... more A series of substituted 2,2′-bipyridine derivatives was prepared using the Kröhnke reaction and alkylation of 4,4′-dimethyl-2,2′-bipyridine. These compounds were screened for fungicidal activity against 9 plant diseases. 5-Phenyl-2,2′-bipyridine exhibited strong preventative ...
CSIRO Moleculur Science P. 0. Bo.r 225, Dicksorz, ACT, 2602, AUSTRALIA Fax +61 2 6276 6628 e-mud:... more CSIRO Moleculur Science P. 0. Bo.r 225, Dicksorz, ACT, 2602, AUSTRALIA Fax +61 2 6276 6628 e-mud: durren.cundy@exec.c.siro.au + I 8-Methyl eicosanoic acid ( 18MEA) has attracted attention as an additive to hair cosmetic compositions because of its ability to impart desirable conditioning effects. We required gram quantities of I8MEA for related studies and surveyed the literature for convenient preparative methods. The earliest description' of the synthesis of I 8MEA reacts cyclopentadecanone with the Grignard reagent derived from k3-methyl bromopentane to afford the corresponding tertiary alcohol. The latter was oxidised in low yield by chromium trioxide to afford the corresponding keto acid which was subsequently reduced by an undisclosed Wolff Kishner procedure to afford the product in 8% overall yield.
Journal of the Chemical Society, Perkin Transactions 1, 1999
Page 1. J. Chem. Soc., Perkin Trans. 1, 1999, 559567 559 An asymmetric synthesis of ADDA and ADD... more Page 1. J. Chem. Soc., Perkin Trans. 1, 1999, 559567 559 An asymmetric synthesis of ADDA and ADDA-glycine dipeptide using the β-lactam synthon method Darren J. Cundy,a Andrew C. Donohuea and Tom D. McCarthya,b*1 ...
A Convenient Large-Scale Preparation of endo-2-Methylbicyclo(2.2.1) hept-5-ene-exo-2-carboxylic A... more A Convenient Large-Scale Preparation of endo-2-Methylbicyclo(2.2.1) hept-5-ene-exo-2-carboxylic Acid.
Tetrahedron Letters, 1998
A range of NH substrates of varying nucleophilicity were reacted with a selection of electronical... more A range of NH substrates of varying nucleophilicity were reacted with a selection of electronically diverse aryl boronic acids in the presence of cupric acetate in order to evaluate the generality of a previously described N-arylation procedure. The results of that investigation are discussed.
Synthetic Communications, 1995
Synthetic Communications, 1993
The title anion readily reacts with a variety of electrophiles to give adducts which, upon treatm... more The title anion readily reacts with a variety of electrophiles to give adducts which, upon treatment with methanol in the presence of p-toluenesulfonic acid, afford the corresponding α-functionalized dimethyl acetals.
Organic Preparations and Procedures International, 1995
Bioorganic & Medicinal Chemistry Letters, 1997
Derivatives of 3- and 1-(4′-hydroxy-3′-(hydroxymethyl)butyl)-imidazo[4,5-b]pyridine were prepared... more Derivatives of 3- and 1-(4′-hydroxy-3′-(hydroxymethyl)butyl)-imidazo[4,5-b]pyridine were prepared in several steps from 2-amino-5-chloropyridine. Selected compounds were evaluated against human cytomeglovirus (HCMV), herpes simplex virusus (HSV1/HSV2) and varicella zoster virus (VZV). Details of their synthesis and biological activities are presented.
Bioorganic & Medicinal Chemistry Letters, 1995
A series of substituted 2,2′-bipyridine derivatives was prepared using the Kröhnke reaction and a... more A series of substituted 2,2′-bipyridine derivatives was prepared using the Kröhnke reaction and alkylation of 4,4′-dimethyl-2,2′-bipyridine. These compounds were screened for fungicidal activity against 9 plant diseases. 5-Phenyl-2,2′-bipyridine exhibited strong preventative ...
CSIRO Moleculur Science P. 0. Bo.r 225, Dicksorz, ACT, 2602, AUSTRALIA Fax +61 2 6276 6628 e-mud:... more CSIRO Moleculur Science P. 0. Bo.r 225, Dicksorz, ACT, 2602, AUSTRALIA Fax +61 2 6276 6628 e-mud: durren.cundy@exec.c.siro.au + I 8-Methyl eicosanoic acid ( 18MEA) has attracted attention as an additive to hair cosmetic compositions because of its ability to impart desirable conditioning effects. We required gram quantities of I8MEA for related studies and surveyed the literature for convenient preparative methods. The earliest description' of the synthesis of I 8MEA reacts cyclopentadecanone with the Grignard reagent derived from k3-methyl bromopentane to afford the corresponding tertiary alcohol. The latter was oxidised in low yield by chromium trioxide to afford the corresponding keto acid which was subsequently reduced by an undisclosed Wolff Kishner procedure to afford the product in 8% overall yield.