Diastereoselective synthesis of β-aminosulfones from the 1,2-addition to N-(para-methoxyphenyl) imines
Author:
Funder
EPSRC
GSK
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference32 articles.
1. Synthesis of β-aminosulfonopeptides activated through selective N-nitration of a taurine amide unit
2. Synthesis and structure–activity relationship of a novel sulfone series of TNF-α converting enzyme inhibitors
3. The identification of potent, selective, and bioavailable cathepsin S inhibitors
4. Potent, orally bioavailable HIV-1 protease inhibitors containing noncoded D-amino acids
5. Reduction of Peptide Character of HIV Protease Inhibitors That Exhibit Nanomolar Potency against Multidrug Resistant HIV-1 Strains
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Metal-free photosensitized aminosulfonylation of alkenes: a practical approach to β-amido sulfones;Green Chemistry;2023
2. Reactions of Aldehydes and Ketones and their Derivatives;Organic Reaction Mechanisms · 2014;2018-01-05
3. ChemInform Abstract: Diastereoselective Synthesis of β-Aminosulfones from the 1,2-Addition to N-(para-methoxyphenyl) Imines.;ChemInform;2015-04
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