Search Results - "Afarinkia, K"

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  1. 1

    Control of the stereochemistry of C14 hydroxyl during the total synthesis of withanolide E and physachenolide C by Anees, M, Nayak, S, Afarinkia, K, Vinader, V

    Published in RSC advances (01-01-2018)
    “…The stereochemical outcome of the epoxidation of Δ cholestanes with mCPBA is controlled by the steric bulk of a C17 substituent. When the C17 is in the β…”
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  2. 2

    Carbasugar probes to explore the enzyme binding pocket at the anomeric position: application to the design of Golgi mannosidase II inhibitors by Vinader, M V, Afarinkia, K

    Published in Current medicinal chemistry (01-10-2013)
    “…A methodology is described for the highly efficient and divergent synthesis of pseudosugars which allows the stereoselective introduction of polar groups at…”
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  3. 3

    Recent advances in the chemistry of azapyranose sugars by Afarinkia, Kamyar, Bahar, Akmal

    Published in Tetrahedron: asymmetry (04-04-2005)
    “…[Display omitted] This report covers the natural occurrence and recent (1998 to 2004) reported syntheses of azapyranose sugars…”
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    An Experimental and Computational Investigation of the Diels−Alder Cycloadditions of Halogen-Substituted 2(H)-Pyran-2-ones by Afarinkia, Kamyar, Bearpark, Michael J, Ndibwami, Alexis

    Published in Journal of organic chemistry (18-02-2005)
    “…Diels−Alder reactions of 3- and 5-halo-subsituted 2(H)-pyran-2-ones with both electron-rich and electron-deficient dienophiles afford stable and readily…”
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  6. 6

    Diels–Alder cycloaddition of 5-aryl-2-pyrones by Afarinkia, Kamyar, Berna-Canovas, Jose

    Published in Tetrahedron letters (19-06-2000)
    “…Regio- and stereoselectivity of the Diels–Alder cycloadditions of a range of 5-aryl-2-pyrones are reported…”
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  7. 7

    Hewitt reaction revisited by Afarinkia, Kamyar, Yu, Hiu-wan

    Published in Tetrahedron letters (20-01-2003)
    “…A range of alkyl phenylphosphonites are prepared from the reaction of phenylphosphinic acid with the corresponding alkyl chloroformates. A mechanism for this…”
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  8. 8

    Computational and Experimental Investigation of the Diels−Alder Cycloadditions of 4-Chloro-2(H)-pyran-2-one by Afarinkia, Kamyar, Bearpark, Michael J, Ndibwami, Alexis

    Published in Journal of organic chemistry (19-09-2003)
    “…4-Chloro-2(H)-pyran-2-one undergoes thermal Diels−Alder cycloaddition with electron-deficient dienophiles to afford, without any significant selectivity,…”
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  9. 9

    A novel and concise synthesis of (±) 2- epi-validamine by Afarinkia, Kamyar, Mahmood, Farzana

    Published in Tetrahedron (05-03-1999)
    “…(±) 2- epi-Validamine has been synthesised in five steps by the chemical manipulation of the bicyclic lactone cycloadduct of ethyl coumalate and vinylene…”
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    Control of electron demand in the cycloadditions of 2( H)-1,4-oxazin-2-ones by Afarinkia, Kamyar, Bahar, Akmal, Neuss, Judi, Vyas, Maushami

    Published in Tetrahedron letters (13-09-2004)
    “…[Display omitted] 3-Methoxy-5-chloro-6-methyl-2( H)-1,4-oxazin-2-one 4 , 3-methoxy-5-chloro-6-phenyl-2( H)-1,4-oxazin-2-one 5 ,…”
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  12. 12

    Preparation of Asymmetric α-Ketophosphonates by [3,3]-Sigmatropic Shift of Enolphosphonates by Afarinkia, Kamyar, Twist, Andrew J, Yu, Hiu-wan

    Published in Journal of organic chemistry (17-09-2004)
    “…α-Ketophosphonates are prepared by a [3,3]-sigmatropic shift of enolphosphonates…”
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  13. 13

    Investigation of the Diels−Alder Cycloadditions of 2(H)-1,4-Oxazin-2-ones by Afarinkia, Kamyar, Bahar, Akmal, Bearpark, Michael J, Garcia-Ramos, Yésica, Ruggiero, Andrea, Neuss, Judi, Vyas, Maushami

    Published in Journal of organic chemistry (11-11-2005)
    “…A variety of 5-chloro-2(H)-1,4-oxazin-2-ones bearing a range of substituents at their 3- and 6-positions undergo Diels−Alder cycloaddition as a 2-azadiene…”
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  14. 14

    Preparation of α-ketophosphonates by a [3,3]-sigmatropoic shift of enolphosphonates by Afarinkia, Kamyar, Twist, Andrew J., Yu, Hiu-wan

    Published in Journal of organometallic chemistry (16-05-2005)
    “…α-Ketophosphonates are prepared by a [3,3]-sigmatropic shift of enolphosphonates. α-Ketophosphonates are prepared by a [3,3]-sigmatropic shift of…”
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  15. 15

    The anionic route to tricyclanes by Afarinkia, Kamyar, Mahmood, Farzana

    Published in Tetrahedron letters (19-02-2000)
    “…A very mild anion induced intramolecular ring closure route to tricyclanes is reported…”
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  16. 16

    Acceleration of nucleophilic addition to vinylphosphonates and vinyl phosphine oxides by chlorotrimethylsilane by Afarinkia, Kamyar, Binch, Hayley M., Modi, Chetna

    Published in Tetrahedron letters (01-10-1998)
    “…Chlorotrimethylsilane significantly accelerates the conjugate addition of alkyl cuprates to vinylphosphonates. Chlorotrimethylsilane significantly accelerates…”
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  17. 17

    Highly efficient Diels-Alder cycloadditions of 2-pyridones with bulky N-sulfonyl substituent by Afarinkia, Kamyar, Mahmood, Farzana

    Published in Tetrahedron letters (29-01-1998)
    “…The rearrangement of N-sulfonyl pyridones to the corresponding O-sulfonyl pyridinols during cycloaddition can be greatly retarded by introduction of steric…”
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  18. 18

    A novel synthesis of (±) 2- epi-validamine by Afarinkia, Kamyar, Mahmood, Farzana

    Published in Tetrahedron letters (01-10-1998)
    “…(±) 2- epi-Validamine is synthesised in five steps by the chemical manipulation of bicyclic lactone cycloadduct of ethyl coumalate and vinylene carbonate…”
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  19. 19

    Conformational preferences in 2-alkyl, 2-alkanoyl and 2-aroyl-2-oxo-1,3,2-oxazaphosphorinanes by Afarinkia, Kamyar, Angell, Richard, Jones, Clare L, Lowman, James

    Published in Tetrahedron letters (22-01-2001)
    “…A series of 2-alkyl-, 2-alkanoyl- and 2-aroyl-2-oxo-1,3,2-oxazaphosphorinanes bearing N-benzyl, N-benzhydryl and N-trityl substituents are prepared and their…”
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  20. 20

    A mild and stereoselective synthesis of β-phosphonylacrylates by Afarinkia, Kamyar, Evans, Marc, Graham, Jocelyn C.H., Jimenez-Bueno, Gorka

    Published in Tetrahedron letters (29-01-1998)
    “…The addition of trimethylsilyloxy phosphorus (III) derivatives, generated in situ, to α-haloacrylates and acrylonitriles at room temperature provides a mild,…”
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