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 inTetrahedron letters Vol. 45; no. 24; pp. 4623 - 4625
Main Authors Suh, BC, Jeon, HB, Posner, GH, Silverman, SM
Format Journal Article
LanguageEnglish
Published OXFORD Elsevier 07.06.2004
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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.
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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Issue 24
Keywords INHIBITION
vitamin D
CALCIFEROL
'click' chemistry
DERIVATIVES
triazole
1-ALPHA,25-DIHYDROXYVITAMIN D-3
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Snippet Cycloaddition of a vitamin D side chain terminal acetylene with phenyl azide and separately with a vitamin D side chain terminal azide produced the...
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SubjectTerms Chemistry
Chemistry, Organic
Physical Sciences
Science & Technology
Title Vitamin D side chain triazole analogs via cycloaddition 'click' chemistry
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