@article{f2133c3b59d44525ab86b8ac74ad7777,
title = "A revised mechanism for chemoselective reduction of esters with borane-dimethyl sulfide complex and catalytic sodium tetrahydroborate directed by adjacent hydroxyl group",
abstract = "The plausible mechanism for the reduction of the ester groups with a strong preference for one located α to the hydroxyl groups of S-malates and R,R-tartrate-based derivatives has been proposed together with some results with regard to its applications to the syntheses of chiral synthons.",
author = "Seiki Saito and Teruhiko Ishikawa and Akiyoshi Kuroda and Kazuya Koga and Toshio Moriwake",
note = "Funding Information: Acknowledgement. We thank to The SC-NMR Laboratory of Okayama University for the high-field (200 Or 500 MHz) NMR experiments. We are grateful to the Ministry of Education, Science, and cuhore, Japan for financial support as a Grant-in-Aid for Scientific Research (No. 60550613).",
year = "1992",
doi = "10.1016/S0040-4020(01)92187-8",
language = "English",
volume = "48",
pages = "4067--4086",
journal = "Tetrahedron",
issn = "0040-4020",
publisher = "Elsevier Limited",
number = "20",
}