@article{397e395eec474e8581010fac2ee6e0bc,
title = "Enantioselective synthesis of valoneic acid derivative",
abstract = "The enantioselective synthesis of trimethyl octa-O-methylvaloneate (1) was accomplished using the Bringmann's 'lactone concept', which involves the intramolecular biaryl coupling reaction of a phenyl benzoate derivative and the asymmetric lactone-opening reaction.",
author = "Hitoshi Abe and Yusuke Sahara and Yuki Matsuzaki and Yasuo Takeuchi and Takashi Harayama",
note = "Funding Information: The authors are indebted to Professor T. Hatano and Dr. H. Ito (Okayama University) for providing the authentic sample of 1 . We thank the SC-NMR Laboratory of Okayama University for the use of their facilities. Part of this work was supported by the Japan Society for the Promotion of Science for H.A. (Grant No. 18590005). ",
year = "2008",
month = jan,
day = "21",
doi = "10.1016/j.tetlet.2007.11.154",
language = "English",
volume = "49",
pages = "605--609",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Limited",
number = "4",
}