Diastereoselection in rhodium-mediated intramolecular C-H insertion: preparation of a trans-3,4 dialkyl cyclopentane
- 31 December 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (26) , 3059-3062
- https://doi.org/10.1016/s0040-4039(00)98618-0
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Synthesis of (dl)-pentalenolactones E and FJournal of the American Chemical Society, 1984
- Stereoisomerism and local chiralityJournal of the American Chemical Society, 1984
- The mechanism and thermodynamics of alkane and arene carbon-hydrogen bond activation in (C5Me5)Rh(PMe3)(R)HJournal of the American Chemical Society, 1984
- Oxidative addition of rhodium to alkane carbon-hydrogen bonds: enhancement in selectivity and alkyl group functionalizationOrganometallics, 1984
- Enantioselective carbocyclization: a facile route to chiral cyclopentanesJournal of the American Chemical Society, 1983
- General route to highly functionalized cyclopentane derivatives by intramolecular C-H insertionThe Journal of Organic Chemistry, 1982
- Cyclopentanone synthesis by intramolecular carbon-hydrogen insertion of diazo ketones. A diterpene-to-steroid skeleton conversionThe Journal of Organic Chemistry, 1982
- A greatly improved procedure for ruthenium tetroxide catalyzed oxidations of organic compoundsThe Journal of Organic Chemistry, 1981
- Alkylation of dianions of .beta.-keto estersJournal of the American Chemical Society, 1974
- Direct introduction of the diazo function in organic synthesisThe Journal of Organic Chemistry, 1968