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Cited by in F6Publishing
For: Liu J, Han J, Izawa K, Sato T, White S, Meanwell NA, Soloshonok VA. Cyclic tailor-made amino acids in the design of modern pharmaceuticals. Eur J Med Chem 2020;208:112736. [PMID: 32966895 DOI: 10.1016/j.ejmech.2020.112736] [Cited by in Crossref: 13] [Cited by in F6Publishing: 7] [Article Influence: 6.5] [Reference Citation Analysis]
Number Citing Articles
1 Han J, Wzorek A, Klika KD, Soloshonok VA. Recommended Tests for the Self-Disproportionation of Enantiomers (SDE) to Ensure Accurate Reporting of the Stereochemical Outcome of Enantioselective Reactions. Molecules 2021;26:2757. [PMID: 34067099 DOI: 10.3390/molecules26092757] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
2 Zou Y, Takeda R, Han J, Konno H, Moriwaki H, Abe H, Izawa K, Soloshonok VA. Asymmetric Synthesis of N ‐Fmoc‐( S )‐7‐aza‐tryptophan via Alkylation of Chiral Nucleophilic Glycine Equivalent. Eur J Org Chem 2021;2021:2962-5. [DOI: 10.1002/ejoc.202100485] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Nagaoka K, Nakano A, Han J, Sakamoto T, Konno H, Moriwaki H, Abe H, Izawa K, Soloshonok VA. Comparative study of different chiral ligands for dynamic kinetic resolution of amino acids. Chirality 2021;33:685-702. [PMID: 34402557 DOI: 10.1002/chir.23350] [Reference Citation Analysis]
4 Della Valle A, Stefanucci A, Scioli G, Szűcs E, Benyhe S, Pieretti S, Minosi P, Sturaro C, Calò G, Zengin G, Mollica A. Selective MOR activity of DAPEA and Endomorphin-2 analogues containing a (R)-γ-Freidinger lactam in position two. Bioorg Chem 2021;115:105219. [PMID: 34343741 DOI: 10.1016/j.bioorg.2021.105219] [Reference Citation Analysis]
5 Han J, Konno H, Sato T, Soloshonok VA, Izawa K. Tailor-made amino acids in the design of small-molecule blockbuster drugs. Eur J Med Chem 2021;220:113448. [PMID: 33906050 DOI: 10.1016/j.ejmech.2021.113448] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 5.0] [Reference Citation Analysis]
6 Liu A, Han J, Nakano A, Konno H, Moriwaki H, Abe H, Izawa K, Soloshonok VA. New pharmaceuticals approved by FDA in 2020: Small-molecule drugs derived from amino acids and related compounds. Chirality 2022;34:86-103. [PMID: 34713503 DOI: 10.1002/chir.23376] [Reference Citation Analysis]
7 Mykhailiuk PK. Fluorine-Containing Prolines: Synthetic Strategies, Applications, and Opportunities. J Org Chem 2022. [PMID: 35175772 DOI: 10.1021/acs.joc.1c02956] [Reference Citation Analysis]
8 Beksultanova N, Gözükara Z, Araz M, Bulut M, Polat-Çakır S, Aygün M, Dogan Ö. FAM-Ag-catalyzed asymmetric synthesis of heteroaryl-substituted pyrrolidines. Chirality 2021;33:465-78. [PMID: 34038573 DOI: 10.1002/chir.23320] [Reference Citation Analysis]
9 Benke Z, Remete AM, Semghouli A, Kiss L. Selective Functionalization of Norbornadiene Through Nitrile Oxide Cycloaddition/Ring‐Opening/Cross‐Metathesis Protocols. Asian J Org Chem 2021;10:1184-91. [DOI: 10.1002/ajoc.202100147] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
10 Semghouli A, Benke Z, Remete AM, Novák TT, Fustero S, Kiss L. Selective Transformation of Norbornadiene into Functionalized Azaheterocycles and β-Amino Esters with Stereo- and Regiocontrol. Chem Asian J 2021. [PMID: 34498420 DOI: 10.1002/asia.202100956] [Reference Citation Analysis]
11 Li W, Kitamura T, Zhou Y, Butler G, Han J, Soloshonok VA. Electrophilic fluorination using PhIO/HF·THF reagent. Journal of Fluorine Chemistry 2020;240:109670. [DOI: 10.1016/j.jfluchem.2020.109670] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Slivka M, Korol N. Synthesis of mononuclear heterocycles via electrophilic cyclization. Monatsh Chem 2022;153:1-8. [DOI: 10.1007/s00706-021-02869-6] [Reference Citation Analysis]
13 Han J, Lyutenko NV, Sorochinsky AE, Okawara A, Konno H, White S, Soloshonok VA. Tailor-Made Amino Acids in Pharmaceutical Industry: Synthetic Approaches to Aza-Tryptophan Derivatives. Chemistry 2021;27:17510-28. [PMID: 34913215 DOI: 10.1002/chem.202102485] [Reference Citation Analysis]