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- W2058992498 abstract "Abstract The [3+2]-cycloaddition reactions of cyclic secondary α-amino acids viz L-proline and (R)-(−)-thiaproline with 5-methylthioisatin via azomethine ylide in the presence of dipolarophiles afford azabicyclooctane derivatives in moderate-to-good yields. The cycloadducts have been characterized by elemental analysis and spectral techniques viz IR, 1H NMR, 13C NMR, MASS. In addition, stereochemical aspects of the cycloaddition have been ascertained by MOPAC-6 calculations using AM1 hamiltonians. Keywords: 1,3-Dipolar cycloaddition reactions5-methylbenzo[b]thiophene-2,3-dioneL-proline(R)-(−)-thiazolidine-4-carboxylic acidsemiempirical calculationsspectral characterization Acknowledgments The authors are thankful to the UGC, New Delhi for financial assistance. B. Gupta is thankful to UGC, New Delhi for NET-JRF Scholarship." @default.
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- W2058992498 date "2004-12-01" @default.
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- W2058992498 title "[3+2]-CYCLOADDITION REACTIONS OF THIOISATIN WITH L-PROLINE AND (R)-(−)-THIAPROLINE" @default.
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- W2058992498 doi "https://doi.org/10.1080/10426500490494372" @default.
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