Recent Developments in the Synthesis of Five- and Six-Membered Heterocycles Using Molecular Iodine
Heterocyclic scaffolds represent the key structural subunits of many biologically active compounds. Over the last few years iodine‐mediated reactions have been extensively studied due to their low cost and eco‐friendliness. This Review covers advances in the field of iodine‐mediated synthesis of het...
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Published in | Chemistry : a European journal Vol. 18; no. 18; pp. 5460 - 5489 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
WILEY-VCH Verlag
27.04.2012
WILEY‐VCH Verlag Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
ISSN | 0947-6539 1521-3765 1521-3765 |
DOI | 10.1002/chem.201100324 |
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Summary: | Heterocyclic scaffolds represent the key structural subunits of many biologically active compounds. Over the last few years iodine‐mediated reactions have been extensively studied due to their low cost and eco‐friendliness. This Review covers advances in the field of iodine‐mediated synthesis of heterocyclic compounds since 2006, especially with an emphasis on mechanisms of ring formation. In this article, syntheses of different heterocycles are classified based on the manipulation of functional groups.
Eco‐friendly iodine: Heterocyclic scaffolds represent the key structural subunits of many biologically active compounds. Over the last few years iodine‐mediated reactions have been extensively studied due to their low cost and eco‐friendliness. This Review covers advances in the field of iodine‐mediated synthesis of heterocyclic compounds since 2006, especially with an emphasis on mechanisms of ring formation. |
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Bibliography: | ark:/67375/WNG-6XRPX1MV-G istex:C215DF45C9DC22A033885E3B907813AA271BDF39 DST ArticleID:CHEM201100324 CSIR ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Review-3 content type line 23 |
ISSN: | 0947-6539 1521-3765 1521-3765 |
DOI: | 10.1002/chem.201100324 |