PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
July 3, 1998Angewandte Chemie International Edition632 citations

trans-RuCl2(phosphane)2(1,2-diamine) and Chiraltrans-RuCl2(diphosphane)(1,2-diamine): Shelf-Stable Precatalysts for the Rapid, Productive, and Stereoselective Hydrogenation of Ketones

View Full Paper
HDHenri DoucetTOTakeshi OhkumaKMKunihiko Murata

Key Points

Key points are not available for this paper at this time.

Abstract

A turnover number (TON) of 2 400 000 and a turnover frequency (TOF) of 63 s-1 are achieved with the chiral RuII complex 1 (R=p-CH3 C6 H4 ) in the asymmetric hydrogenation of acetophenone. Carbonyl-selective asymmetric hydrogenation of α,β-unsaturated ketones proceeds in the presence of these RuII catalysts, and 4-substituted cyclohexanones are selectively converted into cis alcohols.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Doucet et al. (1998) studied this question.

synapsesocial.com/papers/69dab18ba6045d71bfa3dd0ahttps://doi.org/10.1002/(sici)1521-3773(19980703)37:12<1703::aid-anie1703>3.0.co;2-i
Ask AI
Helpful
Bookmark
Share
View Full Paper