An Especially Convenient Stereoselective Reduction of β-Hydroxy Ketones to Anti 1,3 Diols Using Samarium Diiodide
- 6 March 1999
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 64 (7) , 2172-2173
- https://doi.org/10.1021/jo982428a
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Total synthesis of (−)-pironetinTetrahedron Letters, 1998
- BCl3- and TiCl4-Mediated Reductions of β-Hydroxy KetonesThe Journal of Organic Chemistry, 1996
- Chair and twist-boat conformations of 1,3-dioxanes: limitations of molecular mechanics force fieldsThe Journal of Organic Chemistry, 1993
- Studies in polypropionate synthesis: a general approach to the synthesis of stereopentadsTetrahedron Letters, 1992
- Samarium-catalyzed intramolecular Tishchenko reduction of .beta.-hydroxy ketones. A stereoselective approach to the synthesis of differentiated anti 1,3-diol monoestersJournal of the American Chemical Society, 1990
- Directed reduction of .beta.-hydroxy ketones employing tetramethylammonium triacetoxyborohydrideJournal of the American Chemical Society, 1988
- Compounds Related to Podophyllotoxin. XII. Podophyllotoxone, Picropodophyllone and Dehydropodophyllotoxin1Journal of the American Chemical Society, 1960