Preparation of optically active peralkyldiphosphines and their use, as the rhodium(I) complex, in the asymmetric catalytic hydrogenation of ketones

DOI: 10.1016/0022-328X(89)87285-7

Source and publish data:

Journal of Organometallic Chemistry p. 203 - 222 (1989)

Update date:2022-09-26

Topics:

Authors:

Tani, Kazuhide

Suwa, Kenichi

Tanigawa, Eiji

Ise, Tomokazu

Yamagata, Tsuneaki

et al. et al.

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Article abstract of DOI:10.1016/0022-328X(89)87285-7

Two types of the optically active peralkyldiphosphine, 2,3-O-isopropylidene-2,3-dihydroxy-1,4-bis(dialkylphosphino)butane (Rdiop 3) and N-(N'-substituted carbamoyl)-4-dicyclohexylphosphino-2-dicyclohexylphosphinomethylpyrrolidine (R-Cycapp 8), have been p

Full text of DOI:10.1016/0022-328X(89)87285-7

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Article Doi

Preparation of optically active peralkyldiphosphines and their use, as the rhodium(I) complex, in the asymmetric catalytic hydrogenation of ketones

DOI: 10.1016/0022-328X(89)87285-7

Source and publish data:

Authors:

Article abstract of DOI:10.1016/0022-328X(89)87285-7

Full text of DOI:10.1016/0022-328X(89)87285-7

Products guided by the article

R&D Labs maybe for 84409-70-1

Relevant to this article

Synthesis, acetylcholinesterase inhibition and neuroprotective activity of new tacrine analogues

Palladium-Catalyzed Allylic Alkylation of 2-Aryl-1,3-Dithianes, an Umpolung Synthesis of β,γ-Unsaturated Ketones

2-Substituted Tetrahydrofurans of Known Absolute Stereochemistry by SCN' Chirality Transfer

A New Water-soluble Singlet Oxygen Probe

Molecular modulation of muscarinic antagonists. Synthesis and affinity profile of 2,2-diphenyl-2-ethylthio-acetic acid esters designed to probe the binding site cavity

Synthesis of 4-aminomethyl analogs of daphnetin

2-Substituted Tetrahydrofurans of Known Absolute Stereochemistry by S_CN' Chirality Transfer