| Year |
Citation |
Score |
| 2023 |
Lombrea A, Watz CG, Bora L, Dehelean CA, Diaconeasa Z, Dinu S, Turks M, Lugiņina J, Peipiņš U, Danciu C. Enhanced Cytotoxicity and Antimelanoma Activity of Novel Semisynthetic Derivatives of Betulinic Acid with Indole Conjugation. Plants (Basel, Switzerland). 13. PMID 38202344 DOI: 10.3390/plants13010036 |
0.788 |
|
| 2023 |
Burcevs A, Sebris A, Traskovskis K, Chu HW, Chang HT, Jovaišaitė J, Juršėnas S, Turks M, Novosjolova I. Synthesis of Fluorescent C-C Bonded Triazole-Purine Conjugates. Journal of Fluorescence. PMID 37460821 DOI: 10.1007/s10895-023-03337-6 |
0.712 |
|
| 2023 |
Beļaunieks R, Puriņš M, Līpiņa RA, Mishnev A, Turks M. 1,3-Difunctionalization of Propargyl Silanes with Concomitant 1,2-Silyl Shift: Synthesis of Allyl Functionalized Vinyl Silanes. Organic Letters. 25: 4627-4631. PMID 37318959 DOI: 10.1021/acs.orglett.3c01245 |
0.313 |
|
| 2023 |
Lombrea A, Semenescu AD, Magyari-Pavel IZ, Turks M, Lugiņina J, Peipiņš U, Muntean D, Dehelean CA, Dinu S, Danciu C. Comparison of In Vitro Antimelanoma and Antimicrobial Activity of 2,3-Indolo-betulinic Acid and Its Glycine Conjugates. Plants (Basel, Switzerland). 12. PMID 36986941 DOI: 10.3390/plants12061253 |
0.786 |
|
| 2022 |
Leškovskis K, Mishnev A, Novosjolova I, Turks M. SnAr Reactions of 2,4-Diazidopyrido[3,2-]pyrimidine and Azide-Tetrazole Equilibrium Studies of the Obtained 5-Substituted Tetrazolo[1,5-]pyrido[2,3-]pyrimidines. Molecules (Basel, Switzerland). 27. PMID 36431776 DOI: 10.3390/molecules27227675 |
0.738 |
|
| 2021 |
Jeminejs A, Novosjolova I, Bizdēna Ē, Turks M. Nucleophile-nucleofuge duality of azide and arylthiolate groups in the synthesis of quinazoline and tetrazoloquinazoline derivatives. Organic & Biomolecular Chemistry. 19: 7706-7723. PMID 34524320 DOI: 10.1039/d1ob01315g |
0.742 |
|
| 2021 |
Līpiņš DD, Jeminejs A, Novosjolova I, Bizdēna Ē, Turks M. Synthesis of Azido and Triazolyl Purine Ribonucleosides. Current Protocols. 1: e241. PMID 34491626 DOI: 10.1002/cpz1.241 |
0.743 |
|
| 2021 |
Gulbe K, Lugiņina J, Jansons E, Kinens A, Turks M. Metal-free glycosylation with glycosyl fluorides in liquid SO. Beilstein Journal of Organic Chemistry. 17: 964-976. PMID 33981367 DOI: 10.3762/bjoc.17.78 |
0.738 |
|
| 2021 |
Lombrea A, Scurtu AD, Avram S, Pavel IZ, Turks M, Lugiņina J, Peipiņš U, Dehelean CA, Soica C, Danciu C. Anticancer Potential of Betulonic Acid Derivatives. International Journal of Molecular Sciences. 22. PMID 33916089 DOI: 10.3390/ijms22073676 |
0.788 |
|
| 2021 |
Cīrule D, Novosjolova I, Bizdēna Ē, Turks M. 1,2,3-Triazoles as leaving groups: SAr reactions of 2,6-bistriazolylpurines with O- and C-nucleophiles. Beilstein Journal of Organic Chemistry. 17: 410-419. PMID 33633809 DOI: 10.3762/bjoc.17.37 |
0.722 |
|
| 2021 |
Kriķis KĒ, Novosjolova I, Mishnev A, Turks M. 1,2,3-Triazoles as leaving groups in SAr-Arbuzov reactions: synthesis of C6-phosphonated purine derivatives. Beilstein Journal of Organic Chemistry. 17: 193-202. PMID 33564329 DOI: 10.3762/bjoc.17.19 |
0.721 |
|
| 2021 |
Traskovskis K, Sebris A, Novosjolova I, Turks M, Guzauskas M, Volyniuk D, Bezvikonnyi O, Grazulevicius JV, Mishnev A, Grzibovskis R, Vembris A. All-organic fast intersystem crossing assisted exciplexes exhibiting sub-microsecond thermally activated delayed fluorescence Journal of Materials Chemistry C. 9: 4532-4543. DOI: 10.1039/D0TC05099G |
0.632 |
|
| 2021 |
Sebris A, Traskovskis K, Novosjolova I, Turks M. Synthesis and photophysical properties of 2-azolyl-6-piperidinylpurines Chemistry of Heterocyclic Compounds. 57: 560-567. DOI: 10.1007/s10593-021-02943-1 |
0.712 |
|
| 2021 |
Cīrule D, Novosjolova I, Spuris A, Mishnev A, Bizdēna Ē, Turks M. Toward unsymmetrical 2,6-bistriazolylpurine nucleosides Chemistry of Heterocyclic Compounds. 57: 292-297. DOI: 10.1007/s10593-021-02906-6 |
0.698 |
|
| 2021 |
Kapilinskis Z, Novosjolova I, Bizdēna Ē, Turks M. Synthesis of 2-triazolylpurine Phosphonates Chemistry of Heterocyclic Compounds. 57: 55-62. DOI: 10.1007/s10593-021-02867-w |
0.734 |
|
| 2021 |
Beļaunieks R, Puriņš M, Kumpiņš V, Turks M. Synthesis of 3-Silylated 3-Sulfolenes from Propargylsilanes and their Reductive Desulfitation Chemistry of Heterocyclic Compounds. 57: 20-25. DOI: 10.1007/s10593-021-02862-1 |
0.308 |
|
| 2020 |
Jovaisaite J, Cīrule D, Jeminejs A, Novosjolova I, Turks M, Baronas P, Komskis R, Tumkevicius S, Jonusauskas G, Jursenas S. Proof of principle of a purine D-A-D' ligand based ratiometric chemical sensor harnessing complexation induced intermolecular PET. Physical Chemistry Chemical Physics : Pccp. 22: 26502-26508. PMID 33185211 DOI: 10.1039/d0cp04091f |
0.667 |
|
| 2020 |
Waldvogel SR, Blum S, Schollmeyer D, Turks M. Metal- and Reagent-free Electrochemical Synthesis of Alkyl Arylsulfonates in a Multi-Component Reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32338808 DOI: 10.1002/Chem.202001180 |
0.358 |
|
| 2020 |
Gulbe K, Turks M. Synthesis of Sulfones via Ru(II)-Catalyzed Sulfination of Boronic Acids Journal of Organic Chemistry. 85: 5660-5669. PMID 32212658 DOI: 10.1021/Acs.Joc.9B03403 |
0.763 |
|
| 2020 |
Zaķis JM, Ozols K, Novosjolova I, Vilšķērsts R, Mishnev A, Turks M. Sulfonyl Group Dance: A Tool for the Synthesis of 6-Azido-2-sulfonylpurine Derivatives. The Journal of Organic Chemistry. 85: 4753-4771. PMID 32150410 DOI: 10.1021/Acs.Joc.9B03518 |
0.749 |
|
| 2020 |
Matulja D, Wittine K, Malatesti N, Laclef S, Turks M, Markovic MK, Ambrožić G, Marković D. Marine Natural Products with High Anticancer Activities. Current Medicinal Chemistry. 27: 1243-1307. PMID 31931690 DOI: 10.2174/0929867327666200113154115 |
0.317 |
|
| 2020 |
Novosjolova I, Turks M, Jeminejs A, Goliškina SM, Stepanovs D, Bizdēna Ē. Application of Azide-Tetrazole Tautomerism and Arylsulfanyl Group Dance in the Synthesis of Thiosubstituted Tetrazoloquinazolines Synthesis. 53: 1443-1456. DOI: 10.1055/s-0040-1706568 |
0.74 |
|
| 2020 |
Blum SP, Schollmeyer D, Turks M, Waldvogel SR. Cover Feature: Metal‐ and Reagent‐Free Electrochemical Synthesis of Alkyl Arylsulfonates in a Multi‐Component Reaction (Chem. Eur. J. 38/2020) Chemistry: a European Journal. 26: 8315-8315. DOI: 10.1002/Chem.202002881 |
0.376 |
|
| 2019 |
Popov SA, Semenova MD, Baev DS, Frolova TS, Shults EE, Wang C, Turks M. Synthesis of cytotoxic urs-12-ene- and 28-nor-urs-12-ene- type conjugates with amino- and mercapto-1,3,4-oxadiazoles and mercapto-1,2,4-triazoles. Steroids. 108524. PMID 31622615 DOI: 10.1016/j.steroids.2019.108524 |
0.363 |
|
| 2019 |
Šišuļins A, Bucevičius J, Tseng YT, Novosjolova I, Traskovskis K, Bizdēna Ē, Chang HT, Tumkevičius S, Turks M. Synthesis and fluorescent properties of N(9)-alkylated 2-amino-6-triazolylpurines and 7-deazapurines. Beilstein Journal of Organic Chemistry. 15: 474-489. PMID 30873231 DOI: 10.3762/Bjoc.15.41 |
0.735 |
|
| 2019 |
Puriņš M, Mishnev A, Turks MR. Brønsted Acid Catalyzed 1,2-Silyl Shift in Propargyl Silanes: Synthesis of Silyl Dienes and Silyl Indenes. The Journal of Organic Chemistry. 84: 3595-3611. PMID 30784268 DOI: 10.1021/acs.joc.8b02735 |
0.355 |
|
| 2019 |
Šišuļins A, Bizdēna Ē, Turks M, Novosjolova I. 2,6-Bis[4-(4-butylphenyl)-1H-1,2,3-triazol-1-yl]-9-dodecyl-9H-purine Molbank. 2019. DOI: 10.3390/M1073 |
0.683 |
|
| 2018 |
Gerasimova T, Rjabovs V, Turks M. Novel Ciprofloxacin Derivatives for Polymer-Based Drug Delivery Systems Key Engineering Materials. 762: 36-41. DOI: 10.4028/www.scientific.net/KEM.762.36 |
0.714 |
|
| 2018 |
Greitāns K, Rībena D, Turks M. Synthesis of Tetrahydroindazole-Triazole Conjugates and their Derivatization by the Ritter Reaction Key Engineering Materials. 762: 25-30. DOI: 10.4028/www.scientific.net/KEM.762.25 |
0.331 |
|
| 2018 |
Peipiņš V, Suta K, Turks M. Study on Synthesis of N-Protected 2-Triazolyl Azetidines Key Engineering Materials. 762: 19-24. DOI: 10.4028/www.scientific.net/KEM.762.19 |
0.329 |
|
| 2018 |
Kapilinskis Z, Novosjolova I, Turks M. Purine-Furan and Purine-Thiophene Conjugates Molbank. 2018. DOI: 10.3390/M1024 |
0.701 |
|
| 2018 |
Lugiņina J, Vasiļjevs D, Ivanovs I, Mishnev A, Turks M. Diastereoselective aza-Michael addition for synthesis of carbohydrate-derived spiropiperazinones Monatshefte FüR Chemie - Chemical Monthly. 150: 21-28. DOI: 10.1007/s00706-018-2304-x |
0.371 |
|
| 2017 |
Zeltins A, Turks M, Skrastina D, Lugiņina J, Kalnciema I, Balke I, Bizdēna Ē, Skrivelis V. Synthesis and Immunological Evaluation of Virus-Like Particle-Milbemycin A₃/A₄ Conjugates. Antibiotics (Basel, Switzerland). 6. PMID 28892001 DOI: 10.3390/antibiotics6030018 |
0.79 |
|
| 2017 |
Khlebnicova TS, Piven YA, Baranovsky AV, Lakhvich FA, Shishkina SV, Zicāne D, Tetere Z, Rāviņa I, Kumpiņš V, Rijkure I, Mieriņa I, Peipiņš U, Turks M. Synthesis of novel lupane triterpenoid-indazolone hybrids with oxime ester linkage. Steroids. 117: 77-89. PMID 27500691 DOI: 10.1016/j.steroids.2016.08.002 |
0.345 |
|
| 2017 |
Goliškina SM, Cīrule D, Bizdēna Ē, Turks M. Synthesis of 4-Alkylamino-2-Triazolylquinazolines Materials Science and Applied Chemistry. 34. DOI: 10.1515/msac-2017-0009 |
0.311 |
|
| 2017 |
Bucevicius J, Turks M, Tumkevicius S. Easy Access to Isomeric 7-Deazapurine–1,2,3-Triazole Conjugates via SNAr and CuAAC Reactions of 2,6-Diazido-7-deazapurines Synlett. 29: 525-529. DOI: 10.1055/S-0036-1590942 |
0.461 |
|
| 2017 |
Stikute A, Lugiņina J, Turks M. Synthesis of allyl sulfones from potassium allyltrifluoroborates Tetrahedron Letters. 58: 2727-2731. DOI: 10.1016/J.TETLET.2017.05.097 |
0.335 |
|
| 2016 |
Marković D, Tchawou WA, Novosjolova I, Laclef S, Stepanovs D, Turks M, Vogel P. Synthesis and Applications of Silyl 2-Methylprop-2-ene-1-sulfinates in Preparative Silylation and GC-Derivatization Reactions of Polyols and Carbohydrates. Chemistry (Weinheim An Der Bergstrasse, Germany). 22: 4196-205. PMID 26864218 DOI: 10.1002/Chem.201504380 |
0.774 |
|
| 2016 |
Stepanovs D, Tetere Z, Rāviņa I, Kumpiņš V, Zicāne D, Bizdēna Ē, Bogans J, Novosjolova I, Grigaloviča A, Meri RM, Fotins J, Čerkasovs M, Mishnev A, Turks M. Structural characterization of cevimeline and its trans-impurity by single crystal XRD. Journal of Pharmaceutical and Biomedical Analysis. 118: 404-9. PMID 26609680 DOI: 10.1016/J.Jpba.2015.11.006 |
0.656 |
|
| 2016 |
Ozols K, Cīrule D, Novosjolova I, Stepanovs D, Liepinsh E, Bizdēna Ē, Turks M. Development of N6-methyl-2-(1,2,3-triazol-1-yl)-2′-deoxyadenosine as a novel fluorophore and its application in nucleotide synthesis Tetrahedron Letters. 57: 1174-1178. DOI: 10.1016/J.Tetlet.2016.02.003 |
0.729 |
|
| 2016 |
Cīrule D, Ozols K, Platnieks O, Bizdēna Ē, Māliņa I, Turks M. Synthesis of purine nucleoside—amino acid conjugates and their photophysical properties Tetrahedron. 72: 4177-4185. DOI: 10.1016/J.TET.2016.05.043 |
0.303 |
|
| 2016 |
Stipniece L, Salma-Ancane K, Rjabovs V, Juhnevica I, Turks M, Narkevica I, Berzina-Cimdina L. Development of functionalized hydroxyapatite/poly(vinyl alcohol) composites Journal of Crystal Growth. 444: 14-20. DOI: 10.1016/J.Jcrysgro.2016.03.029 |
0.72 |
|
| 2016 |
Luginina J, Turks M. Non-Activated Aziridines As Building Blocks For The Synthesis Of Aza-Heterocycles Chemistry of Heterocyclic Compounds. 52: 773-775. DOI: 10.1007/3412 |
0.803 |
|
| 2016 |
Markovic D, Tchawou WA, Novosjolova I, Laclef S, Stepanovs D, Turks M, Vogel P. Synthesis and Applications of Silyl 2-Methylprop-2-ene-1-sulfinates in Preparative Silylation and GC-Derivatization Reactions of Polyols and Carbohydrates Chemistry - a European Journal. 22: 4196-4205. DOI: 10.1002/chem.201504380 |
0.774 |
|
| 2015 |
Semjonovs N, Rjabovs V, Stepanovs D, Turks M. Crystal structure of 3-O-benzyl-4(R)-C-(1-benzyl-1H-1,2,3-triazol-4-yl)-1,2-O-iso-propyl-idene-α-d-erythro-furan-ose. Acta Crystallographica. Section E, Crystallographic Communications. 71: 1542-4. PMID 26870425 DOI: 10.1107/S2056989015022434 |
0.751 |
|
| 2015 |
Rjabovs V, Stepanovs D, Turks M. Crystal structure of 3-C-(N-benzyl-oxy-carbon-yl)amino-methyl-3-de-oxy-1,2:5,6-di-O-iso-propyl-idene-α-d-allo-furan-ose. Acta Crystallographica. Section E, Crystallographic Communications. 71: 1212-5. PMID 26594409 DOI: 10.1107/S2056989015017582 |
0.757 |
|
| 2015 |
Brovkina J, Shulga G, Ozolins J, Irbe Z, Turks M, Rjabovs V. Characteristics of the Coagulate Obtained During the Process of Model Wastewater Treatment Environment. Technology. Resources. Proceedings of the International Scientific and Practical Conference. 1: 9. DOI: 10.17770/ETR2013VOL1.799 |
0.699 |
|
| 2015 |
Novosjolova I, Turks M. User Friendly Synthesis of Vogel’S Silyl Sulfinate and its Application in Quantitative Gc–Ms Analysis Phosphorus Sulfur and Silicon and the Related Elements. 190: 1251-1256. DOI: 10.1080/10426507.2014.996644 |
0.675 |
|
| 2015 |
Novosjolova I, Bizdēna Ē, Turks M. Synthesis of Novel 2- and 6-Alkyl/Arylthiopurine Derivatives Phosphorus Sulfur and Silicon and the Related Elements. 190: 1236-1241. DOI: 10.1080/10426507.2014.989435 |
0.754 |
|
| 2015 |
Stikute A, Peipiņš V, Turks M. Synthesis of allyl sulfoxides from allylsilanes via silyl sulfinates Tetrahedron Letters. 56: 4578-4581. DOI: 10.1016/J.TETLET.2015.06.018 |
0.344 |
|
| 2015 |
Grigorjeva J, Uzuleņa J, Rjabovs V, Turks M. Synthesis of monomeric methylene-linked 1,2,3-triazole glycoconjugates from allo- and glucofuranoses Chemistry of Heterocyclic Compounds. 51: 883-890. DOI: 10.1007/s10593-015-1791-5 |
0.769 |
|
| 2015 |
Uzuleņa J, Rjabovs V, Moreno-Vargas AJ, Turks M. Synthesis of 1,2,3-triazole-linked glycohybrids in the gluco-, gulo-, and allopyranose series Chemistry of Heterocyclic Compounds. 51: 664-671. DOI: 10.1007/s10593-015-1754-x |
0.766 |
|
| 2015 |
Rjabovs V, Ostrovskis P, Posevins D, Kiseļovs G, Kumpiņš V, Mishnev A, Turks M. Synthesis of Building Blocks for Carbopeptoids and Their Triazole Isoster Assembly European Journal of Organic Chemistry. 2015: 5572-5584. DOI: 10.1002/EJOC.201500695 |
0.722 |
|
| 2015 |
Novosjolova I, Bizdēna Ē, Turks M. Synthesis and Applications of Azolylpurine and Azolylpurine Nucleoside Derivatives European Journal of Organic Chemistry. 2015: 3629-3649. DOI: 10.1002/Ejoc.201403527 |
0.729 |
|
| 2015 |
Stikute A, Peipins V, Turks M. ChemInform Abstract: Synthesis of Allyl Sulfoxides from Allylsilanes via Silyl Sulfinates. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201545105 |
0.341 |
|
| 2015 |
Novosjolova I, Bizdena E, Turks M. ChemInform Abstract: Synthesis and Applications of Azolylpurine and Azolylpurine Nucleoside Derivatives Cheminform. 46: no-no. DOI: 10.1002/CHIN.201534262 |
0.734 |
|
| 2014 |
Rjabovs V, Mishnev A, Kiselovs G, Turks M. {(3aR,5S,6R,6aR)-5-[(R)-1,2-Di-hydroxy-eth-yl]-2,2-di-methyl-tetra-hydro-furo[2,3-d][1,3]dioxol-6-yl}methyl methane-sulfonate. Acta Crystallographica. Section E, Structure Reports Online. 70: o524-5. PMID 24860338 DOI: 10.1107/S1600536814007387 |
0.716 |
|
| 2014 |
Turks M, Vēze K, Kiseļovs G, Mackeviča J, Lugiņina J, Mishnev A, Marković D. Synthesis and X-ray studies of novel 3-C-nitromethyl-hexofuranoses. Carbohydrate Research. 391: 82-8. PMID 24785391 DOI: 10.1016/j.carres.2014.03.003 |
0.809 |
|
| 2014 |
Novosjolova I, Stepanovs D, Bizdēna E, Mishnev A, Turks M. 2,6-Di-chloro-9-(2',3',5'-tri-O-acetyl-β-d-ribo-furanos-yl)-9H-purine. Acta Crystallographica. Section E, Structure Reports Online. 70: o108-9. PMID 24764840 DOI: 10.1107/S1600536813034521 |
0.685 |
|
| 2014 |
Mackeviča J, Ostrovskis P, Leffler H, Nilsson UJ, Rudovica V, Viksna A, Belyakov S, Turks M. Synthesis of 1,2,3-triazole-linked galactohybrids and their inhibitory activities on galectins Arkivoc. 2014: 90-112. DOI: 10.3998/Ark.5550190.P008.402 |
0.31 |
|
| 2014 |
Novosjolova I, Bizdēna Ē, Mandrika I, Petrovska R, Kloviņš J, Turks M. Biological activity profile of triazolylpurine nucleosides Collection of Czechoslovak Chemical Communications. 14: 337-339. DOI: 10.1135/Css201414337 |
0.641 |
|
| 2014 |
Novosjolova I, Bizdēna Ē, Turks M. Derivatives of 2,6-diazidopurine and 2,6-bis-(1,2,3-triazol-1-yl) purine as useful intermediates in the synthesis of modified purine nucleosides Collection of Czechoslovak Chemical Communications. 14: 332-336. DOI: 10.1135/Css201414332 |
0.746 |
|
| 2014 |
Cīrule D, Ozols K, Novosjolova I, Turks M, Bizdēna Ē. A Synthetic Route to 2,6-Bis-triazolyl Purine Deoxynucleosides via Click Chemistry Collection of Czechoslovak Chemical Communications. 14: 233-235. DOI: 10.1135/Css201414233 |
0.715 |
|
| 2014 |
Šišuļins A, Novosjolova I, Turks M, Bizdēna Ē. Synthesis of new fluorescent 9-alkyl-6-amino-2-triazolyl purines Collection of Czechoslovak Chemical Communications. 14: 231-232. DOI: 10.1135/Css201414231 |
0.713 |
|
| 2014 |
Novosjolova I, Bizdēna Ē, Turks M. CorrigendumCorrigendum to “Application of 2,6-diazidopurine derivatives in the synthesis of thiopurine nucleosides” [Tetrahedron Lett. 54 (2013) 6557–6561] Tetrahedron Letters. 55: 4972. DOI: 10.1016/J.Tetlet.2014.07.052 |
0.73 |
|
| 2014 |
Kalniņa A, Bizdēna Ē, Kiselovs G, Mishnev A, Turks M. Structural Proof of Tetrazolo[1,5-a]quinazoline Derivatives and their Application in the Synthesis of 4-Amino-2-(1,2,3-triazol-1-yl)quinazolines* Chemistry of Heterocyclic Compounds. 49: 1667-1673. DOI: 10.1007/s10593-014-1418-2 |
0.309 |
|
| 2014 |
Kalnina A, Bizdena E, Kiselovs G, Mishnev A, Turks M. ChemInform Abstract: Structural Proof of Tetrazolo[1,5-a]quinazoline Derivatives and Their Application in the Synthesis of 4-Amino-2-(1,2,3-triazol-1-yl)quinazolines. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201424179 |
0.319 |
|
| 2014 |
Rjabovs V, Turks M. ChemInform Abstract: Tetrahydrofuran Amino Acids of the Past Decade Cheminform. 45: no-no. DOI: 10.1002/CHIN.201410264 |
0.716 |
|
| 2014 |
Luginina J, Rjabovs V, Belyakov S, Turks M. ChemInform Abstract: A Concise Synthesis of Sugar Isoxazole Conjugates. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201407134 |
0.768 |
|
| 2013 |
Novosjolova I, Bizdēna Ē, Belyakov S, Turks M. The Synthesis and X-ray Studies of 6-pyrrolidinyl-2-triazolyl Purine Arabinonucleoside Materials Science and Applied Chemistry. 28: 39-44. DOI: 10.7250/Msac.2013.007 |
0.698 |
|
| 2013 |
Turks M, Streļņikova N, Kumpiņš V, Kalējs U. Synthesis of Enantiomerically Enriched 1,2,3- Triazole-derivatized Homoalanines Material Science and Applied Chemistry. 28: 21. DOI: 10.7250/MSAC.2013.004 |
0.343 |
|
| 2013 |
Novosjolova I, Bizdēna Ē, Turks M. Application of 2,6-diazidopurine derivatives in the synthesis of thiopurine nucleosides Tetrahedron Letters. 54: 6557-6561. DOI: 10.1016/J.Tetlet.2013.09.095 |
0.765 |
|
| 2013 |
Lugiņina J, Rjabovs V, Belyakov S, Turks M. A concise synthesis of sugar isoxazole conjugates Tetrahedron Letters. 54: 5328-5331. DOI: 10.1016/J.TETLET.2013.07.103 |
0.768 |
|
| 2013 |
Kovaļovs A, Novosjolova I, Bizdēna Ē, Bižāne I, Skardziute L, Kazlauskas K, Jursenas S, Turks M. 1,2,3-Triazoles as leaving groups in purine chemistry: a three-step synthesis of N6-substituted-2-triazolyl-adenine nucleosides and photophysical properties thereof Tetrahedron Letters. 54: 850-853. DOI: 10.1016/J.Tetlet.2012.11.095 |
0.751 |
|
| 2013 |
Rjabovs V, Turks M. Tetrahydrofuran amino acids of the past decade Tetrahedron. 69: 10693-10710. DOI: 10.1016/J.TET.2013.10.021 |
0.71 |
|
| 2013 |
Ayatollahi S, Kalnina D, Song W, Turks M, Cooper WJ. Radiation chemistry of salicylic and methyl substituted salicylic acids: Models for the radiation chemistry of pharmaceutical compounds Radiation Physics and Chemistry. 92: 93-98. DOI: 10.1016/J.Radphyschem.2013.06.007 |
0.303 |
|
| 2013 |
Zicāne D, Tetere Z, Rāviņa I, Turks M. Synthesis of Novel 4-Aminotetrahydropyrrolo[1,2-a]quinazoline Derivatives Chemistry of Heterocyclic Compounds. 49: 310-316. DOI: 10.1007/s10593-013-1248-7 |
0.355 |
|
| 2012 |
Lugiņina J, Rjabovs V, Belyakov S, Turks M. On Moffatt dehydration of glucose-derived nitro alcohols. Carbohydrate Research. 350: 86-9. PMID 22281179 DOI: 10.1016/j.carres.2011.12.020 |
0.778 |
|
| 2012 |
Rjabova J, Rjabovs V, Moreno Vargas A, Clavijo E, Turks M. Synthesis of novel 3-deoxy-3-C-triazolylmethyl-allose derivatives and evaluation of their biological activity Open Chemistry. 10: 386-394. DOI: 10.2478/s11532-012-0002-9 |
0.764 |
|
| 2011 |
Exner CJ, Turks M, Fonquerne F, Vogel P. Concise synthesis of complicated polypropionates through one-pot dissymmetrical two-directional chain elongation. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 4246-53. PMID 21387431 DOI: 10.1002/Chem.201003264 |
0.473 |
|
| 2011 |
Exner CJ, Laclef S, Poli F, Turks M, Vogel P. Total asymmetric syntheses of β-hydroxy-δ-lactones via Umpolung with sulfur dioxide. The Journal of Organic Chemistry. 76: 840-5. PMID 21218837 DOI: 10.1021/Jo102035D |
0.425 |
|
| 2011 |
Strakova I, Kumpiņa I, Rjabovs V, Lugiņina J, Belyakov S, Turks M. Resolution, absolute configuration, and synthetic transformations of 7-amino-tetrahydroindazolones Tetrahedron: Asymmetry. 22: 728-739. DOI: 10.1016/J.TETASY.2011.03.010 |
0.709 |
|
| 2011 |
Turks M, Fairweather KA, Scopelliti R, Vogel P. Efficient Asymmetric Synthesis of Long-Chain Polyketides Containing up to Ten Contiguous Stereogenic Centres by Double Chain Elongation European Journal of Organic Chemistry. 2011: 3317-3328. DOI: 10.1002/Ejoc.201100196 |
0.469 |
|
| 2010 |
Laclef S, Turks M, Vogel P. Total synthesis and determination of the absolute configuration of (-)-dolabriferol. Angewandte Chemie (International Ed. in English). 49: 8525-7. PMID 20865714 DOI: 10.1002/Anie.201003735 |
0.502 |
|
| 2010 |
Laclef S, Turks M, Vogel P. Totalsynthese und Bestimmung der absoluten Konfiguration von (−)-Dolabriferol Angewandte Chemie. 122: 8704-8706. DOI: 10.1002/Ange.201003735 |
0.411 |
|
| 2009 |
Laclef S, Exner CJ, Turks M, Videtta V, Vogel P. Synthesis of (E,Z)-1-alkoxy-3-acyloxy-2-methylpenta-1,3-dienes via Danishefsky-type dienes or O-acylation of enones. The Journal of Organic Chemistry. 74: 8882-5. PMID 19842642 DOI: 10.1021/Jo901878B |
0.44 |
|
| 2009 |
Turks M, Vogel P. Synthesis of optically active 5-alkoxy-6-methylcyclohex-2-en-1-ones and 4-alkoxy-5-methylcyclopent-1-enyl benzoate. The Journal of Organic Chemistry. 74: 435-7. PMID 19012433 DOI: 10.1021/Jo801981C |
0.429 |
|
| 2009 |
Vogel P, Turks M, Exner C, Hamel C. Umpolung with Sulfur Dioxide: Carbon-Carbon Cross-Coupling of Electron-Rich 1,3-Dienes and Alkenes; Application to the Enantioselective Synthesis of Long-Chain Polyketide Fragments Synthesis. 2009: 1065-1074. DOI: 10.1055/S-0028-1088011 |
0.46 |
|
| 2008 |
Vogel P, Turks M, Bouchez L, Craita C, Murcia MC, Fonquerne F, Didier C, Huang X, Flowers C. Use of sultines in the asymmetric synthesis of polypropionate antibiotics Pure and Applied Chemistry. 80: 791-805. DOI: 10.1351/Pac200880040791 |
0.518 |
|
| 2007 |
Vogel P, Turks M, Bouchez L, Marković D, Varela-Alvarez A, Sordo JA. New organic chemistry of sulfur dioxide. Accounts of Chemical Research. 40: 931-42. PMID 17685582 DOI: 10.1021/Ar700096H |
0.489 |
|
| 2007 |
Turks M, Vogel P. Synthesis of Enantiomerically Enriched 2-Substituted Pyrrolidine Analogues of Norhygrine. Application of the Hetero-Diels—Alder Addition of Sulfur Dioxide. Cheminform. 38. DOI: 10.3987/Com-06-S(K)38 |
0.478 |
|
| 2007 |
Turks M, Vogel P. Synthesis of Enantiomerically Enriched 2-Substituted Pyrrolidine Analogues of Norhygrine. Application of the Hetero-Diels—Alder Addition of Sulfur Dioxide. Cheminform. 38. DOI: 10.1002/CHIN.200739196 |
0.363 |
|
| 2006 |
Turks M, Lawrence AK, Vogel P. The bora-ene reaction of sulfur dioxide and prop-2-ene-1-boronic esters. New route to sulfoxides Tetrahedron Letters. 47: 2783-2786. DOI: 10.1016/J.Tetlet.2006.02.071 |
0.501 |
|
| 2006 |
Bouchez LC, Turks M, Dubbaka SR, Fonquerne F, Craita C, Laclef S, Vogel P. Sulfur Dioxide Mediated One-Pot, Four-Component Synthesis of Polyfunctional Sulfones and Sulfonamides, Including Medium-Ring Cyclic Derivatives. Cheminform. 37. DOI: 10.1016/J.Tet.2005.08.067 |
0.535 |
|
| 2006 |
Bouchez LC, Turks M, Dubbaka SR, Fonquerne F, Craita C, Laclef S, Vogel P. Sulfur Dioxide Mediated One-Pot, Four-Component Synthesis of Polyfunctional Sulfones and Sulfonamides, Including Medium-Ring Cyclic Derivatives. Cheminform. 37. DOI: 10.1002/CHIN.200612066 |
0.308 |
|
| 2005 |
Turks M, Huang X, Vogel P. Expeditious asymmetric synthesis of a stereoheptad corresponding to the C(19)-C(27)-ansa chain of rifamycins: formal total synthesis of Rifamycin S. Chemistry (Weinheim An Der Bergstrasse, Germany). 11: 465-76. PMID 15551311 DOI: 10.1002/Chem.200400825 |
0.484 |
|
| 2005 |
Craita C, Bouchez L, Turks M, Huang X, Fonquerne F, Murcia MC, Vogel P. Total Synthesis of Polypropionate Natural Products: Application of New Sulfur Dioxide Chemistry Cheminform. 36. DOI: 10.1080/10426500590910828 |
0.467 |
|
| 2004 |
Bouchez LC, Dubbaka SR, Turks M, Vogel P. Sulfur dioxide mediated one-pot, three- and four-component syntheses of polyfunctional sulfonamides and sulfonic esters: study of the stereoselectivity of the ene reaction of sulfur dioxide. The Journal of Organic Chemistry. 69: 6413-8. PMID 15357602 DOI: 10.1021/Jo049047J |
0.5 |
|
| 2004 |
Turks M, Murcia MC, Scopelliti R, Vogel P. First asymmetric synthesis of the cyclohexanone subunit of baconipyrones A and B. Revision of its structure. Organic Letters. 6: 3031-4. PMID 15330580 DOI: 10.1021/Ol048988F |
0.473 |
|
| 2004 |
Turks M, Fonquerne F, Vogel P. Synthesis of long-chain polyketide fragments by reaction of 1,3-dioxy-1,3-dienes with allylsilanes: umpolung with sulfur dioxide. Organic Letters. 6: 1053-6. PMID 15012098 DOI: 10.1021/Ol0498646 |
0.477 |
|
| Show low-probability matches. |