Vitamin D side chain triazole analogs via cycloaddition 'click' chemistry
Cycloaddition of a vitamin D side chain terminal acetylene with phenyl azide and separately with a vitamin D side chain terminal azide produced the corresponding 1,2,3-triazole monomeric and dimeric analogs of 1alpha-hydroxyvitamin D-3 in good yields. (C) 2004 Published by Elsevier Ltd.
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Published in | Tetrahedron letters Vol. 45; no. 24; pp. 4623 - 4625 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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Abstract | Cycloaddition of a vitamin D side chain terminal acetylene with phenyl azide and separately with a vitamin D side chain terminal azide produced the corresponding 1,2,3-triazole monomeric and dimeric analogs of 1alpha-hydroxyvitamin D-3 in good yields. (C) 2004 Published by Elsevier Ltd. |
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AbstractList | Cycloaddition of a vitamin D side chain terminal acetylene with phenyl azide and separately with a vitamin D side chain terminal azide produced the corresponding 1,2,3-triazole monomeric and dimeric analogs of 1alpha-hydroxyvitamin D-3 in good yields. (C) 2004 Published by Elsevier Ltd. |
Author | Jeon, HB Silverman, SM Suh, BC Posner, GH |
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Keywords | INHIBITION vitamin D CALCIFEROL 'click' chemistry DERIVATIVES triazole 1-ALPHA,25-DIHYDROXYVITAMIN D-3 |
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Title | Vitamin D side chain triazole analogs via cycloaddition 'click' chemistry |
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