@article{0ff2c77c889c4d23976ec8114103f080,
title = "Efficient reduction of sulfoxides with 2,6-dihydroxypyridine",
abstract = "2,6-Dihydroxypyridine was found to be an efficient reagent in the deoxygenation of sulfoxides. The mild reaction conditions were compatible with functional groups such as ester and carbamate. It was also found that approximately 0.25 equivalents of 2,6-dihydroxypyridine was required for effective reduction. (C) 2000 Elsevier Science Ltd.",
keywords = "Pyridines, Reduction, Sulfides, Sulfoxides",
author = "Miller, {Samantha J.} and Collier, {Talia R.} and Weiming Wu",
note = "Funding Information: This investigation was supported by a {\textquoteleft}Research Infrastructure in Minority Institutions{\textquoteright} award from the National Center for Research Resources with funding from the Office of Research on Minority Health, National Institutes of Health No. 5 P20 RR11805. We are indebted to Dr. Clifford Berkman and Mr. Wee Tam (SFSU) for assisting us on the use of gas chromatography and obtaining NMR spectra, respectively. We thank Dr. Ihsan Erden (SFSU) for helpful discussions. We also thank Ms. Venus Manalo (CCSF) for her assistance in the laboratory.",
year = "2000",
month = may,
day = "21",
doi = "10.1016/S0040-4039(00)00502-5",
language = "English (US)",
volume = "41",
pages = "3781--3783",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Limited",
number = "20",
}