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Inside Cover: Iodine‐Catalyzed Highly Diastereoselective Synthesis of trans ‐2,6‐Disubstituted‐3,4‐Dihydropyrans: Application to Concise Construction of C28–C37 Bicyclic Core of (+)‐Sorangicin A (Chem. Eur. J. 7/2010)
Author(s) -
Mohapatra Debendra K.,
Das Pragna P.,
Pattanayak Manas Ranjan,
Yadav J. S.
Publication year - 2010
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201090023
Subject(s) - iodine , dihydropyran , chemistry , cover (algebra) , catalysis , ring (chemistry) , stereochemistry , combinatorial chemistry , bicyclic molecule , organic chemistry , engineering , mechanical engineering
A double iodocyclization is reported by D. K. Mohapatra, J. S. Yadav et al. in the Full Paper on page 2072 ff. A novel iodine‐catalyzed highly diastereoselective synthesis of trans ‐2,6‐disubstituted‐3,4‐dihydropyran ring system has been achieved that can be utilized for the synthesis of diversified complex biologically active natural products.