Efficient Asymmetric Synthesis of Novel 4-Substituted and Configurationally Stable Analogues of Thalidomide-Reference-Cited by-同舟云学术

Efficient Asymmetric Synthesis of Novel 4-Substituted and Configurationally Stable Analogues of Thalidomide

Published:2006-10-26 Issue:24 Volume:8 Page:5625-5628
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Yamada Takeshi¹,Okada Takuya¹,Sakaguchi Kazuhiko¹,Ohfune Yasufumi¹,Ueki Hisanori¹,Soloshonok Vadim A.¹

Affiliation:

1. Graduate School of Science, Osaka City University, Japan, and Department of Chemistry and Biochemistry, The University of Oklahoma, Norman, Oklahoma 73019

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol0623668

Reference36 articles.

1. Tumor Angiogenesis: A Possible Control Point in Tumor Growth

2. Thalidomide selectively inhibits tumor necrosis factor alpha production by stimulated human monocytes.

3. Thalidomide exerts its inhibitory action on tumor necrosis factor alpha by enhancing mRNA degradation.

4. Thalidomide and dexamethasone: therapy for multiple myeloma

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