One-Pot Synthesis of (S)-Baclofen via Aldol Condensation of Acetaldehyde with Diphenylprolinol Silyl Ether Mediated Asymmetric Michael Reaction as a Key Step-Reference-Cited by-同舟云学术

One-Pot Synthesis of (S)-Baclofen via Aldol Condensation of Acetaldehyde with Diphenylprolinol Silyl Ether Mediated Asymmetric Michael Reaction as a Key Step

Published:2015-12-04 Issue:1 Volume:18 Page:4-7
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Hayashi Yujiro¹,Sakamoto Daisuke¹,Okamura Daichi¹

Affiliation:

1. Department of Chemistry, Graduate School of Science, Tohoku University, 6-3 Aramaki-Aza Aoba-ku, Sendai, Miyagi 980-8578, Japan

Funder

Ministry of Education, Culture, Sports, Science, and Technology

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.5b02839

Reference55 articles.

1. Combining pot, atom and step economy (PASE) in organic synthesis. Synthesis of tetrahydropyran-4-ones

2. One-Pot Reactions Accelerate the Synthesis of Active Pharmaceutical Ingredients

3. Pot Economy in the Synthesis of Prostaglandin A1and E1Methyl Esters

4. One‐Pot High‐Yielding Synthesis of the DPP4‐Selective Inhibitor ABT‐341 by a Four‐Component Coupling Mediated by a Diphenylprolinol Silyl Ether

5. High-Yielding Synthesis of the Anti-Influenza Neuramidase Inhibitor (−)-Oseltamivir by Three “One-Pot” Operations

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