Conversion of leucomycin-A3 antibiotic into novel triazole analogues via regio- and diastereoselective SN1′ substitution with allylic rearrangement and 1,3-dipolar cycloaddition of CuAAC type-Reference-Cited by-同舟云学术

Conversion of leucomycin-A3 antibiotic into novel triazole analogues via regio- and diastereoselective SN1′ substitution with allylic rearrangement and 1,3-dipolar cycloaddition of CuAAC type

Published:2016-04 Issue:15 Volume:57 Page:1661-1666
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Domagalska Joanna,Pyta Krystian,Przybylski Piotr^ORCID

Funder

Narodowe Centrum Nauki

Bank for International Settlements

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference54 articles.

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