Stereoselective addition of Grignard reagents to (2-methyl-5-tert-butyl)phenyl 1-thio-β-D-ribopentodialdo-1,4-furanoside derivative-Reference-Cited by-同舟云学术

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Stereoselective addition of Grignard reagents to (2-methyl-5-tert-butyl)phenyl 1-thio-β-D-ribopentodialdo-1,4-furanoside derivative

Published:2017-04 Issue:16 Volume:73 Page:2290-2304
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Ren Huanming,Xie Wuchen,Xiong Bing,Shen Jingkang,Chen Guohua,Chen Yue-Lei

Funder

National Natural Science Foundation of China

National Science & Technology Major Project “Key New Drug Creation and Manufacturing Program”, China

Strategic Priority Research Program of the Chinese Academy of Sciences

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference24 articles.

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4. Repairing faulty genes by aminoglycosides: Identification of new pharmacophore with enhanced suppression of disease-causing nonsense mutations

5. Boron-Zinc Exchange in The Diastereoselective Arylation of Sugar-Based Aldehydes: Stereoselective Synthesis of (+)-7-epi-Goniofufurone and Analogues

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2. Convenient preparation of pinometostat and related 5′-deoxy-5′-amino adenosine derivatives as well as their activity against DOT1L;Tetrahedron Letters;2018-01

3. Efficient syntheses of alpha- and beta-C-nucleosides and the origin of anomeric selectivity;Organic Chemistry Frontiers;2018

4. Preparation of 5′-deoxy-5′-amino-5′- C -methyl adenosine derivatives and their activity against DOT1L;Bioorganic & Medicinal Chemistry Letters;2017-11

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