Affiliation:
1. Interdisciplinary Research Center for Catalytic Chemistry National Institute of Advanced Industrial Science and Technology Central 5, 1-1-1 Higashi Tsukuba Ibaraki 305-8565 Japan
2. Research Center for Materials Science Nagoya University Chikusa Nagoya 464-8602 Japan
Abstract
AbstractAsymmetric Pd‐catalyzed Tsuji‐Trost‐type allylation is an important catalytic reaction toward chiral natural and unnatural product syntheses. We successfully modified a desalt‐type reaction using allyl ester or halide to a dehydrative one using allylic alcohol via the establishment of two redox‐mediated donor acceptor bifunctional catalyst systems. These systems were cationic CpRu‐Cl‐Napy‐PyCOOH and cationic CpRu‐Naph‐diPIM‐dioxo‐iPr/p‐TsOH and were designed on the basis of the soft ruthenium and hard Brønsted acid combined catalyst concept. The complementary use of the two chiral catalysts for dehydrative asymmetric allylation expands the application scope facilitating the utilization of both aliphatic and aromatic allylic alcohols with various nucleophiles in the substrate. In this account, the design, synthesis, and application of these catalysts were reported.
Funder
Japan Agency for Medical Research and Development
Japan Science and Technology Agency
Naito Foundation
Subject
Materials Chemistry,General Chemical Engineering,Biochemistry,General Chemistry
Cited by
8 articles.
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