Highly enantioselective construction of tertiary thioethers and alcohols via phosphine-catalyzed asymmetric γ-addition reactions of 5H-thiazol-4-ones and 5H-oxazol-4-ones: scope and mechanistic understandings

Author:

Wang Tianli1234,Yu Zhaoyuan5678,Hoon Ding Long1234,Huang Kuo-Wei910111213,Lan Yu5678,Lu Yixin1234

Affiliation:

1. Department of Chemistry

2. National University of Singapore

3. Singapore 117543

4. Singapore

5. School of Chemistry and Chemical Engineering

6. Chongqing University

7. Chongqing 400030

8. P. R. China

9. Division of Physical Sciences and Engineering

10. KAUST Catalysis Center

11. King Abdullah University of Science and Technology

12. Thuwal 23955-6900

13. Saudi Arabia

Abstract

A new method for facile access to enantioenriched tertiary thioethers/alcohols.

Funder

National University of Singapore

Ministry of Education - Singapore

GlaxoSmithKline

Economic Development Board - Singapore

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Reference149 articles.

1. A. Thuillier and P.Metzner, Sulfur Reagents in Organic Synthesis, ed. A. R. Katritzky, O. Meth-Cohn and C. S. Rees, Academic Press, 1995

2. Organosulfur Chemistry in Asymmetric Synthesis, ed. T. Toru and C. Bolm, Wiley-VCH, Weinheim, 2008

3. C. Chatgilialoglu and K.-D.Asmus, Sulfur-Centered Reactive Intermediates in Chemistry and Biology, Springer, 1991

4. J. M. Berg , J. L.Tymoczko and L.Stryer, Biochemistry, Freeman, 5th edn, 2002

5. Thiols in Cellular Redox Signalling and Control

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