Peroxygenase-catalysed selective and scalable synthesis of 25-hydroxy-grundmann's ketone and its derivatives
暂无分享,去创建一个
Xiaoxiao Liu | Wuyuan Zhang | Xiaoying Zhou | Jiandong Cui | Yunhan Zhang | Bishuang Chen | Yalan Zhang | Yawen Huang
[1] X. Xu,et al. Selective oxyfunctionalisation reactions catalysed by P450 monooxygenases and peroxygenases – a bright future for sustainable chemical synthesis , 2022, Current Opinion in Green and Sustainable Chemistry.
[2] E. Kallay,et al. The Effect of Vitamin D and Its Analogs in Ovarian Cancer , 2022, Nutrients.
[3] F. Kasagi,et al. Effect of active vitamin D treatment on development of type 2 diabetes: DPVD randomised controlled trial in Japanese population , 2022, BMJ.
[4] Wuyuan Zhang,et al. Peroxygenase-Catalyzed Selective Synthesis of Calcitriol Starting from Alfacalcidol , 2022, Antioxidants.
[5] Wuyuan Zhang,et al. Enzymatic Hydroxylations of sp3-Carbons , 2021, ACS Catalysis.
[6] G. Grogan. Hemoprotein Catalyzed Oxygenations: P450s, UPOs, and Progress toward Scalable Reactions , 2021, JACS Au.
[7] Wuyuan Zhang,et al. Valorization of Small Alkanes by Biocatalytic Oxyfunctionalization. , 2021, ChemSusChem.
[8] Wuyuan Zhang,et al. C–H bond functionalization reactions enabled by photobiocatalytic cascades , 2021, Green Synthesis and Catalysis.
[9] S. Park,et al. Large-Scale Synthesis of Eldecalcitol , 2020, Organic Process Research & Development.
[10] G. Poelarends,et al. Current state and future perspectives of engineered and artificial peroxygenases for the oxyfunctionalization of organic molecules , 2020, Nature Catalysis.
[11] M. Alcalde,et al. Recent developments in the use of peroxygenases – Exploring their high potential in selective oxyfunctionalisations , 2020, Biotechnology advances.
[12] S. Fernández,et al. Strategies for the Synthesis of 19-nor-Vitamin D Analogs , 2020, Pharmaceuticals.
[13] Jian Sun,et al. Total synthesis of 1α,25-dihydroxy-2β-(3-hydroxypropoxy)vitamin D3 (ED-71) , 2020 .
[14] J. Adams,et al. Vitamin D Binding Protein and the Biological Activity of Vitamin D , 2019, Front. Endocrinol..
[15] C. Carlberg,et al. Vitamin D and Its Synthetic Analogs , 2019, Journal of medicinal chemistry.
[16] Glenville Jones,et al. Update on pharmacologically-relevant vitamin D analogues. , 2018, British journal of clinical pharmacology.
[17] Frank Hollmann,et al. Biocatalytic Oxidation Reactions: A Chemist's Perspective , 2018, Angewandte Chemie.
[18] K. Nagasawa,et al. A-Ring Synthons of 19-Nor Type Vitamin D Derivatives , 2017, The Journal of Steroid Biochemistry and Molecular Biology.
[19] M. Maestro,et al. A new approach to 19-nor-A-ring phosphine oxide for the convergent synthesis of 19-nor-calcitriol , 2017, The Journal of Steroid Biochemistry and Molecular Biology.
[20] H. DeLuca,et al. Design, synthesis and biological properties of seco-d-ring modified 1α,25-dihydroxyvitamin D3 analogues , 2017, The Journal of Steroid Biochemistry and Molecular Biology.
[21] N. Jehmlich,et al. A Peroxygenase from Chaetomium globosum Catalyzes the Selective Oxygenation of Testosterone , 2017, Chembiochem : a European journal of chemical biology.
[22] R. D. Buck,et al. 2MD (DP001), a Single Agent in the Management of Hemodialysis Patients: A Randomized Trial , 2016, American Journal of Nephrology.
[23] J. Rodriguez-Perez,et al. Asymmetric Dimethylarginine (ADMA) Levels Are Lower in Hemodialysis Patients Treated With Paricalcitol , 2016, Kidney international reports.
[24] V. Guallar,et al. Molecular determinants for selective C25-hydroxylation of vitamins D2 and D3 by fungal peroxygenases , 2016 .
[25] V. Guallar,et al. Steroid Hydroxylation by Basidiomycete Peroxygenases: a Combined Experimental and Computational Study , 2015, Applied and Environmental Microbiology.
[26] A. Gutiérrez,et al. Regioselective Hydroxylation in the Production of 25‐Hydroxyvitamin D by Coprinopsis cinerea Peroxygenase , 2015 .
[27] V. Urlacher,et al. Whole-cell biotransformation with recombinant cytochrome P450 for the selective oxidation of Grundmann's ketone. , 2014, Bioorganic & medicinal chemistry.
[28] J. Bergquist,et al. Synthesis of C-11 linked active ester derivatives of vitamin D3 and their conjugations to 42-residue helix–loop–helix peptides , 2010 .
[29] Clara Gómez-Reino,et al. Pd-catalyzed carbocyclization-Negishi cross-coupling cascade: a novel approach to 1alpha,25-dihydroxyvitamin D3 and analogues. , 2005, Organic letters.
[30] C. Wolf,et al. Dissection of NADPH-cytochrome P450 oxidoreductase into distinct functional domains. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[31] E. Mincione,et al. Oxidation of natural targets by dioxiranes. 2. Direct hydroxylation at the side chain C-25 of cholestane derivatives and of vitamin D3 Windaus-Grundmann ketone , 1992 .
[32] M. Uskoković,et al. Stereoselective total synthesis of 1.alpha.,25-dihydroxycholecalciferol , 1982 .
[33] A. Norman,et al. Vitamin D: 3-deoxy-lalpha-hydroxyvitamin D3, biologically active analog of lalpha-dihydroxyvitamin D3. , 1975, Science.