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Practical Synthesis of Dirhodium (II) Tetrakis[N-phthaloyl-(S)-tert-leucinate]
TSUTSUI, Hideyuki
ABE, Takumi
NAKAMURA, Seiichi
ANADA, Masahiro
HASHIMOTO, Shunichi
Location: http://hdl.handle.net/2115/26434
Chemical & pharmaceutical bulletin. 53(10), 2005, 1366-1368

An efficient and reliable procedure for the preparation of dirhodium(II) tetrakis[N-phthaloyl-(S)-tert-leuci-nate], Rh_2(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.

Belongs to: Hokkaido University Collection of Scholarly and Academic Papers

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Practical Synthesis of Dirhodium (II) Tetrakis[N-phthaloyl-(S)-tert-leucinate]
Id. 26873104
Idioma inglés
Titulo Practical Synthesis of Dirhodium (II) Tetrakis[N-phthaloyl-(S)-tert-leucinate]
Autor(es) TSUTSUI, Hideyuki
ABE, Takumi
NAKAMURA, Seiichi
ANADA, Masahiro
HASHIMOTO, Shunichi
Location http://hdl.handle.net/2115/26434
Chemical & pharmaceutical bulletin. 53(10), 2005, 1366-1368
Versión 1.0
Estado Final
Descripción An efficient and reliable procedure for the preparation of dirhodium(II) tetrakis[N-phthaloyl-(S)-tert-leuci-nate], Rh_2(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.
Palabras clave tert-leucine
Tipo de recurso article
Tipo de Interactividad Expositivo
Nivel de Interactividad muy bajo
Audiencia Estudiante
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Estructura Atomic
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Fecha de contribución 26-oct-2007
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