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Studies towards the Total Synthesis of Cruentaren B
Author(s) -
Yadav Jhillu Singh,
Reddy Ailuri Ramesh
Publication year - 2018
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.201802090
Subject(s) - epoxide , stereoselectivity , total synthesis , nucleophile , chemistry , ring (chemistry) , stereochemistry , prins reaction , combinatorial chemistry , organic chemistry , catalysis
Abstract A highly stereoselective and an efficient approach for studies towards the synthesis of Cruentaren B has been described. The key steps involved in this synthesis are Prins cyclisation, nucleophilic epoxide ring opening, Alder‐Rickert reaction, SN 2 displacement reaction and Lindlar's hydrogenation.