670a515b3ffd0.pdf
DOI:
Mavjud emas
[1] Uma Maheshwar G., Jhillu S.Y. Synthesis of Chiral Propargyl Alcohols Following the Base-Induced Elimination Protocol: Application in the Total Synthesis of Natural Products // New Journal of Chemistry, 2020. Volume 44, No13, pp. 4972-4986.[2] Jade V., Maria J. GonzalezS., Nicholas C.and Beatriz M. Catalytic Enantioselective Addition of Alkylzirconium Reagents to Aliphatic Aldehydes //Molecules, 2021. Volume 26,pp. 4471-4499.[3] Robert P., Maciej S. and Jacek M.Propargylation of CoQ0 throught the Redox Chain Reaction //The Journal of Organic Chemistry, 2022. Volume 87, pp. 683-692.[4]Pei Zh., Qiuhong H., Yuyu Ch., Rongshi L., Pengfei L., Wenjun L.Remote Stereocontrolled Construction of Vicinal Axially Chiral Tetrasubstituted Allenes and Heteroatom-Functionalized Quaternary Carbon Stereocenters // Organic Letter, 2019. Volume 21, No2, pp. 503-507.[5] Bowen J., Xiangyu Y., Yong X., Natalya L., Heriberto D.V.,Yanyan G., Ye Y.and Francis V. Tandem Reactions Based on the Cyclization of CarbonDioxide and Propargylic Alcohols: Derivative Applications ofα-Alkylidene Carbonates //Catalysts,2022. Volume 12, No1, pp. 1-35.[6] Jiang S., Du S., Yang R., Jin F., Zhou Z.-Z., Tian W.-F., Song X.-R. and Xiao Q. Brønsted Acid Promoted Sulfonylation of Propargylic Alcohols: Synthesis of Triaryl Allenyl Sulfones under Mild Conditions //European Journal Organic Chemistry,2023. e202201377. [7]Hao An, Shifei Liu, Shao-Jie Wang, Xiaoyi Yu, Chenqi Shi, Haonan Lin, Si Bei Poh, Hui Yang, Ming Wah Wong, Yu Zhao, Zhifeng Tu, and Shenci Lu. Kinetic Resolution of Acyclic Tertiary Propargylic Alcohols by NHC Catalyzed Enantioselective Acylation //Organic Letters,2024.Volume 26, Issue3, pp. 702-707.[8] Kentaro Iwaki, Koki Maruno, Osamu Nagata, and Norio Shibata. Ethynyl-SF4-Pyridines: Reagents for SF4-Alkynylation to Carbonyl Compounds // The Journal of Organic Chemistry, 2022.Volume87, Issue9, 6302-6311.[9]Ziyadullaev O., Otamukhamedova G., Ikramov A., Abdurakhmanova S., Boytemirov O.Synthesis Of Aromatic Acetylene Alcohols Using Complex Catalytic Systems //Chemistry and Chemical Engineering,2021.No2, pp.58-72.[10]Michal R., Stanislaw L., Piotr K.Highly Enantioselective Addition of Phenylethynylzinc to Aldehydes Using Aziridine-Functionalized Tridentate Sulfinyl Ligands//Tetrahedron:Asymmetry,2010.Volume 21, pp. 2687-2689[11]Chen Sh.-Y., Liu W.,Wu. X., Ying J., Yu X., Pu L.A Lewis acid activated reaction of Zn with EtI topromote highly enantioselective alkyne additionsto aldehydes //Chemical Communication, 2015. Volume 51, pp. 358-361. [12]Zhang A.-L., Yang L.-W., Yang N.-F., Liu D.-C.Investigation of catalytic activity and catalytic mechanism of chiral amino diol tridentate ligands in the asymmetric addition of aldehydes in the present of methyllithium reagent // Journal of Organometallic Chemistry, 2014. Volume 768, pp. 50-55. [13]Bauer T. Enantioselective dialkylzinc-mediated alkynylation, arylation and alkenylation of carbonyl groups // Coordination Chemistry Reviews, 2015.Volume 299, pp. 83-150.[14]Moore D. and PuL. BINOL-Catalyzed Highly EnantioselectiveTerminal Alkyne Additions to AromaticAldehydes // OrganicLetters, 2002.Volume 4, No11, pp. 1855-1857.[15] Gao G., Xie R.-G., and Pu L. Highly enantioselective alkyne additions to aldehydes in the presence of 1,1-bi-2-naphthol and hexamethylphosphoramide. // The Proceedingsof the National Academy of Sciences,2004. Volume101, No15, pp. 5417-5424.[16]Xiao-Pu Fu,Li Liu,Dong Wang,Yong-Jun Chen, Chao-Jun Li“On water”-promoted direct alkynylation of isatins catalyzed by NHC–silver complexes for the efficient synthesis of 3-hydroxy-3-ethynylindolin-2-ones // Green Chemistry, 2011. Volume 13, Issue 3, pp. 549-553.[17]Pierre de Fremont, Natalie M. Scott, EdwinD. Stevens, Taramatee Ramnial, Owen C. Lightbody, Charles L. B. Macdonald, Jason A. C. Clyburne, Colin D. Abernethy, Steven P. Nolan Synthesis of Well-Defined N-Heterocyclic Carbene Silver(I) Complexes // Organometallics, 2005. Volume 24, Issue 26, pp. 6301-6309.[18]Taramatee Ramnial, Colin D. Abernethy, Mark D. Spicer, Iain D. McKenzie, Ian D. Gay, Jason A. C. Clyburne A Monomeric Imidazol-2-ylidene−Silver(I) Chloride Complex: Synthesis, Structure, and Solid State 109Ag and 13C CP/MAS NMR Characterization // Inorganic Chemistry, 2003. Volume 42, Issue 5, pp. 1391-1393.[19] Karen J. Ardila-Fierro, Carsten Bolm, Jose G. Hernandez Mechanosynthesis of Odd-Numbered Tetraaryl[n]cumulenes // Angewandte Chemie International Edition, 2019.Volume 58, Issue 37, pp. 12945-12949. [20] Konstantin S. Rodygin, Yulia A. Vikenteva, Valentine P. Ananikov Calcium-Based Sustainable Chemical Technologies for Total Carbon Recycling // Chemistry-Sustainability-Energy-Materials, 2019. Volume 12, Issue 8, pp. 1483-1516.[21] OtamuxamedovaG.Q., Ziyadullayev O.E., Shmid E., Maniecki T. Enantioselectivealkynylation of some cyclical ketones by 3,3′-diphenylbinaphtol dilithium //Chemicaland Chemical Engineering, 2019.2, pp. 30-36.[22] Отамухамедова Г.К., Зиядуллаев О.Э., Буриев Ф.Х., Аблакулов Л.К.Aлкинилирование некоторых кетонов в присутствии октина-1/ Всероссийская научная школа-конференция “Марковниковские чтения:Органическая химия От марковникова до наших дней”, 2024. С. 86