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Статті в журналах з теми "Aza-Heterocycles- Synthesis"
Chamberlain, Anna E. R., Kieran J. Paterson, Roly J. Armstrong, Heather C. Twin, and Timothy J. Donohoe. "A hydrogen borrowing annulation strategy for the stereocontrolled synthesis of saturated aza-heterocycles." Chemical Communications 56, no. 24 (2020): 3563–66. http://dx.doi.org/10.1039/d0cc00903b.
Повний текст джерелаRulev, A. Yu, and A. R. Romanov. "Unsaturated polyfluoroalkyl ketones in the synthesis of nitrogen-bearing heterocycles." RSC Advances 6, no. 3 (2016): 1984–98. http://dx.doi.org/10.1039/c5ra23759a.
Повний текст джерелаZonker, Benjamin, Ediz Duman, Heike Hausmann, Jonathan Becker, and Radim Hrdina. "[1,2]-Rearrangement of iminium salts provides access to heterocycles with adamantane scaffold." Organic & Biomolecular Chemistry 18, no. 26 (2020): 4941–45. http://dx.doi.org/10.1039/d0ob01156h.
Повний текст джерелаSingh, Deepak, and Hyun-Joon Ha. "Metal-free aza-Claisen type ring expansion of vinyl aziridines: an expeditious synthesis of seven membered N-heterocycles." Organic & Biomolecular Chemistry 17, no. 12 (2019): 3093–97. http://dx.doi.org/10.1039/c8ob03029d.
Повний текст джерелаFrontier, Alison J., Shukree Abdul-Rashed, and Connor Holt. "Alkynyl Prins and Alkynyl Aza-Prins Annulations: Scope and Synthetic Applications." Synthesis 52, no. 14 (April 9, 2020): 1991–2007. http://dx.doi.org/10.1055/s-0039-1690869.
Повний текст джерелаGusar, N. I. "Synthesis of heterocycles by the aza-Wittig reaction." Russian Chemical Reviews 60, no. 2 (February 28, 1991): 146–61. http://dx.doi.org/10.1070/rc1991v060n02abeh001036.
Повний текст джерелаYang, Xu-Heng, Jian Huang, Fang Wang, Zhuoliang Liu, Yujiao Li, Cheng-an Tao, and Jianfang Wang. "Copper-catalyzed alkynylation/annulation cascades of N-allyl ynamides: regioselective access to medium-sized N-heterocycles." Organic Chemistry Frontiers 8, no. 1 (2021): 18–24. http://dx.doi.org/10.1039/d0qo00837k.
Повний текст джерелаGuin, Soumitra, Debashis Majee, and Sampak Samanta. "Unmasking the reverse reactivity of cyclic N-sulfonyl ketimines: multifaceted applications in organic synthesis." Chemical Communications 57, no. 72 (2021): 9010–28. http://dx.doi.org/10.1039/d1cc03439a.
Повний текст джерелаSeath, Ciaran P., Kirsty L. Wilson, Angus Campbell, Jenna M. Mowat, and Allan J. B. Watson. "Synthesis of 2-BMIDA 6,5-bicyclic heterocycles by Cu(i)/Pd(0)/Cu(ii) cascade catalysis of 2-iodoaniline/phenols." Chemical Communications 52, no. 56 (2016): 8703–6. http://dx.doi.org/10.1039/c6cc04554e.
Повний текст джерелаNguyen, Thi Thu Tram, Le Anh Nguyen, Quoc Anh Ngo, Marina Koleski, and Thanh Binh Nguyen. "The catalytic role of elemental sulfur in the DMSO-promoted oxidative coupling of methylhetarenes with amines: synthesis of thioamides and bis-aza-heterocycles." Organic Chemistry Frontiers 8, no. 7 (2021): 1593–98. http://dx.doi.org/10.1039/d0qo01654c.
Повний текст джерелаДисертації з теми "Aza-Heterocycles- Synthesis"
McGonagle, Alison Elizabeth. "Synthesis of nitrogen-containing heterocycles using novel aza-Wittig methodology." Thesis, University of Leeds, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.439563.
Повний текст джерелаRace, Nicholas J. "Development of aza-Heck cyclisations for the synthesis of chiral nitrogen heterocycles." Thesis, University of Bristol, 2015. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.681733.
Повний текст джерелаFaulkner, Adele. "Development of aza-Heck cyclisations and cascades for the synthesis of nitrogen heterocycles." Thesis, University of Bristol, 2015. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.687438.
Повний текст джерелаHazelden, Ian. "Development of new classes of aza-Heck cyclisation for the synthesis of nitrogen heterocycles." Thesis, University of Bristol, 2019. http://hdl.handle.net/1983/58bca1bd-9538-4c94-9295-6da0b49eb3b2.
Повний текст джерелаLepitre, Thomas. "Modulation des Processus Domino au départ des Accepteurs de Michael en série Chromone : Diversité par aza-Cyclisation, Arylation et Aryloxylation Métallocatalysées : Diversité par aza-Cyclisation, Arylation et Aryloxylation Métallocatalysées." Thesis, Normandie, 2017. http://www.theses.fr/2017NORMLH31/document.
Повний текст джерелаIn the early 2000s a general consensus has emerged in which the molecular diversity within a given library of small molecules, rather than its size, has been recognized as a crucial requirement. Diversity-oriented synthesis (DOS) has emerged from this new paradigm. This novel approach aims to generate collections of small molecules with high degrees of structural diversity, in the most efficient way, starting from simple building-blocks. Since the generation of collections of structurally diverse small molecules in a DOS-driven approach constitutes a real challenge, diverse strategies have been set up for this purpose.In this line, this work has shed light on the great potential of a domino process as a valuable tool in a DOS-driven strategy, capable of generating both molecular diversity and architectural complexity. This study has been focused on the 3-formylchromone building block, a particular framework which has already proven being an exceptionally versatile precursor of molecular diversity. In this manuscript, we will highlight how it is possible to modulate the course of a domino process to achieve high degrees of molecular diversity, starting from the chromone based 1,6-Michael acceptors platform and primary amines as reaction partners. In particular we will show how it is feasible to control the course of particular steps involved in the domino process through: (I) the pertinent modulation of the Michael acceptors and the primary amines structures, (II) the modulation of the reaction parameters (solvent, temperature, additives), and (III) the tuning of the reactivity within a key reaction intermediate induced by the introduction of an external agent
Jha, Abadh Kishor. "New strategies towards the functionalization of C-H and C-Cl bond of Aryls(Heteroaryls) and synthesis of Aza-Heterocycles." Thesis, 2018. http://eprint.iitd.ac.in:80//handle/2074/7941.
Повний текст джерелаКниги з теми "Aza-Heterocycles- Synthesis"
D’hooghe, Matthias, and Hyun-Joon Ha. Synthesis of 4- to 7-membered Heterocycles by Ring Expansion: Aza-, oxa- and thiaheterocyclic small-ring systems. Springer, 2015.
Знайти повний текст джерелаD’hooghe, Matthias, and Hyun-Joon Ha. Synthesis of 4- to 7-membered Heterocycles by Ring Expansion: Aza-, oxa- and thiaheterocyclic small-ring systems. Springer, 2019.
Знайти повний текст джерелаHa, Hyun-Joon, and Matthias D'hooghe. Synthesis of 4- to 7-Membered Heterocycles by Ring Expansion: Aza-, Oxa- and Thiaheterocyclic Small-Ring Systems. Springer London, Limited, 2015.
Знайти повний текст джерелаЧастини книг з теми "Aza-Heterocycles- Synthesis"
Fort, Yves, and Corinne Comoy. "Lithiated Aza-Heterocycles in Modern Synthesis." In Lithium Compounds in Organic Synthesis, 423–62. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527667512.ch15.
Повний текст джерелаZwanenburg, Binne, and Peter ten Holte. "The Synthetic Potential of Three-Membered Ring Aza-Heterocycles." In Stereoselective Heterocyclic Synthesis III, 93–124. Berlin, Heidelberg: Springer Berlin Heidelberg, 2001. http://dx.doi.org/10.1007/3-540-44726-1_3.
Повний текст джерела"Diastereoselective and Enantioselective Construction of Aza-Heterocycles." In Organic Synthesis, 138–39. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/0470056312.ch70.
Повний текст джерела"Recent Trends in Metal Nanoparticles (MNPs) Catalyzed Synthesis of Aza- and Oxa-Heterocycles." In Advanced Nanocatalysis for Organic Synthesis and Electroanalysis, edited by Tejas M. Dhameliya, Rutvi J. Patel, Normi D. Gajjar, Rajvi H. Amin, Kunjan B. Bodiwala, and Dipen K. Sureja, 114–57. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/9789815040166122010009.
Повний текст джерелаSingh, Girija S., and Tumelo H. Tabane. "Synthetic Approaches to Small- and Medium-Size Aza-Heterocycles in Aqueous Media." In Green Synthetic Approaches for Biologically Relevant Heterocycles, 163–84. Elsevier, 2015. http://dx.doi.org/10.1016/b978-0-12-800070-0.00007-4.
Повний текст джерелаSingh, Girija S. "An update on synthetic methods for small and medium aza-heterocycles in aqueous media." In Green Synthetic Approaches for Biologically Relevant Heterocycles, 505–35. Elsevier, 2021. http://dx.doi.org/10.1016/b978-0-12-820792-5.00011-1.
Повний текст джерелаТези доповідей конференцій з теми "Aza-Heterocycles- Synthesis"
Rosa, Fernanda A., Michael J. V. da Silva, Davana S. Gonçalves, Daniela H. Arita, Camila S. S. Tozatti, and Gisele de F. G. Bandoch. "Synthetic Application of New Enaminodiketone: Regioespecific Synthesis of Aza-Heterocycles." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013101145054.
Повний текст джерела