Diastereo‐ and Enantioselective Hydrogenation of α‐Amino‐β‐Keto Ester Hydrochlorides Catalyzed by an Iridium Complex with MeO‐BIPHEP and NaBAr F : Catalytic Cycle and Five‐Membered Chelation Mechanism of Asymmetric Hydrogenation-Reference-Cited by-同舟云学术

Diastereo‐ and Enantioselective Hydrogenation of α‐Amino‐β‐Keto Ester Hydrochlorides Catalyzed by an Iridium Complex with MeO‐BIPHEP and NaBAr F : Catalytic Cycle and Five‐Membered Chelation Mechanism of Asymmetric Hydrogenation

Published:2010-09-03 Issue:39 Volume:16 Page:11954-11962
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chemistry – A European Journal

Author:

Maeda Tsukuru¹,Makino Kazuishi¹,Iwasaki Masamichi¹,Hamada Yasumasa¹

Affiliation:

1. Graduate School of Pharmaceutical Sciences, Chiba University, Yayoi‐cho, Inage‐ku, Chiba 263‐8522 (Japan), Fax: (+81) 43‐290‐2987

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201001298

Reference101 articles.

1. For reviews of dynamic kinetic resolution see:

2. Stereoselective Organic Synthesis via Dynamic Kinetic Resolution

3. Dynamic kinetic resolution

4. Dynamic kinetic resolution

5. Effizienz in der nichtenzymatischen kinetischen Racematspaltung

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