Abstract
An efficient and reliable procedure for the preparation of dirhodium(II) tetrakis[N-phthaloyl-(S)-tert-leucinate], Rh2(S-PTTL)4, a universally effective catalyst for a range of enantioselective carbene transformations, is described. The N-phthaloylation of (S)-tert-leucine by the method of Bose with essentially no racemization is a key to this process. © 2005 Pharmaceutical Society of Japan.
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Tsutsui, H., Abe, T., Nakamura, S., Anada, M., & Hashimoto, S. (2005). Practical synthesis of dirhodium(II) tetrakis[N-phthaloyl-(S)- tertleucinate]. Chemical and Pharmaceutical Bulletin, 53(10), 1366–1368. https://doi.org/10.1248/cpb.53.1366
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