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Inside Cover: Total Synthesis of (+)‐Haplophytine (Angew. Chem. Int. Ed. 41/2009)
Author(s) -
Ueda Hirofumi,
Satoh Hitoshi,
Matsumoto Koji,
Sugimoto Kenji,
Fukuyama Tohru,
Tokuyama Hidetoshi
Publication year - 2009
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.200904021
Subject(s) - int , cover (algebra) , polymer science , chemistry , engineering , computer science , mechanical engineering , programming language
An oxidative rearrangment and the Fischer indole synthesis are key processes in the first total synthesis of (+)‐haplophytine, which is described by H. Tokuyama, T. Fukuyama, and co‐workers in their Communication on page 7600 ff. The cover picture shows a photograph of Haplophyton cimicidum (T. Beth Kinsey, www.fireflyflrest.com/flowers), which is the source of (+)‐haplophytine.