Catalytic Enantioselective Synthesis of Key Intermediates for Triazole Antifungal Agents-Reference-Cited by-同舟云学术

Catalytic Enantioselective Synthesis of Key Intermediates for Triazole Antifungal Agents

Published:2005-06-01 Issue:13 Volume:7 Page:2527-2530
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Suzuki Masato¹,Kato Nobuki¹,Kanai Motomu¹,Shibasaki Masakatsu¹

Affiliation:

1. Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo 113-0033, Japan, and PRESTO, Japan Science and Technology Corporation, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol050398%2B

Reference17 articles.

1. Oral Azole Drugs as Systemic Antifungal Therapy

2. Synthesis of Novel Azole Antifungals by a Modified Sharpless Asymmetric Dihydroxylation

3. Enantioselective synthesis of the optical isomers of broad-spectrum orally active antifungal azoles, Sch 42538 and Sch 45012

4. PPL-catalyzed enzymatic asymmetrization of a 2-substituted prochiral 1,3-diol with remote chiral functionality: Improvements toward synthesis of the eutomers of SCH 45012

5. A practical chemoenzymatic synthesis of a key intermediate of antifungal agents

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