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The protective group was removed and the double bond was dihydroxylated leading to the target compound. Removal of the protective group was performed using a newly found ecofriendly catalyst for N\u2010Boc deprotection. The final iminosugar derivative 7 and all newly synthesized intermediates, were investigated against S. aureus and E. coli bacteria and were found to show promising activity against both gram\u2010positive and gram\u2010negative bacteria.\n                  <\/jats:p>","DOI":"10.1002\/slct.201903190","type":"journal-article","created":{"date-parts":[[2019,12,6]],"date-time":"2019-12-06T03:22:26Z","timestamp":1575602546000},"page":"13384-13387","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Synthesis and Bioactivity of New Analogue of Bicyclic 1\u2010Azafagomine"],"prefix":"10.1002","volume":"4","author":[{"given":"Fidan N.","family":"Akhundova","sequence":"first","affiliation":[{"name":"Baku State University Organic Chemistry Department  Z. Khalilov 23 Baku AZ 1148"}]},{"given":"Malahat M.","family":"Kurbanova","sequence":"additional","affiliation":[{"name":"Baku State University Organic Chemistry Department  Z. 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