Artículos de revistas sobre el tema "Aza-Heterocycles- Synthesis"
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Chamberlain, Anna E. R., Kieran J. Paterson, Roly J. Armstrong, Heather C. Twin y Timothy J. Donohoe. "A hydrogen borrowing annulation strategy for the stereocontrolled synthesis of saturated aza-heterocycles". Chemical Communications 56, n.º 24 (2020): 3563–66. http://dx.doi.org/10.1039/d0cc00903b.
Texto completoRulev, A. Yu y A. R. Romanov. "Unsaturated polyfluoroalkyl ketones in the synthesis of nitrogen-bearing heterocycles". RSC Advances 6, n.º 3 (2016): 1984–98. http://dx.doi.org/10.1039/c5ra23759a.
Texto completoZonker, Benjamin, Ediz Duman, Heike Hausmann, Jonathan Becker y Radim Hrdina. "[1,2]-Rearrangement of iminium salts provides access to heterocycles with adamantane scaffold". Organic & Biomolecular Chemistry 18, n.º 26 (2020): 4941–45. http://dx.doi.org/10.1039/d0ob01156h.
Texto completoSingh, Deepak y 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, n.º 12 (2019): 3093–97. http://dx.doi.org/10.1039/c8ob03029d.
Texto completoFrontier, Alison J., Shukree Abdul-Rashed y Connor Holt. "Alkynyl Prins and Alkynyl Aza-Prins Annulations: Scope and Synthetic Applications". Synthesis 52, n.º 14 (9 de abril de 2020): 1991–2007. http://dx.doi.org/10.1055/s-0039-1690869.
Texto completoGusar, N. I. "Synthesis of heterocycles by the aza-Wittig reaction". Russian Chemical Reviews 60, n.º 2 (28 de febrero de 1991): 146–61. http://dx.doi.org/10.1070/rc1991v060n02abeh001036.
Texto completoYang, Xu-Heng, Jian Huang, Fang Wang, Zhuoliang Liu, Yujiao Li, Cheng-an Tao y Jianfang Wang. "Copper-catalyzed alkynylation/annulation cascades of N-allyl ynamides: regioselective access to medium-sized N-heterocycles". Organic Chemistry Frontiers 8, n.º 1 (2021): 18–24. http://dx.doi.org/10.1039/d0qo00837k.
Texto completoGuin, Soumitra, Debashis Majee y Sampak Samanta. "Unmasking the reverse reactivity of cyclic N-sulfonyl ketimines: multifaceted applications in organic synthesis". Chemical Communications 57, n.º 72 (2021): 9010–28. http://dx.doi.org/10.1039/d1cc03439a.
Texto completoSeath, Ciaran P., Kirsty L. Wilson, Angus Campbell, Jenna M. Mowat y 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, n.º 56 (2016): 8703–6. http://dx.doi.org/10.1039/c6cc04554e.
Texto completoNguyen, Thi Thu Tram, Le Anh Nguyen, Quoc Anh Ngo, Marina Koleski y 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, n.º 7 (2021): 1593–98. http://dx.doi.org/10.1039/d0qo01654c.
Texto completoZhang, Yong-Sheng, Xiang-Ying Tang y Min Shi. "Unprecedented synthesis of aza-bridged benzodioxepine derivatives through a tandem Rh(ii)-catalyzed 1,3-rearrangement/[3+2] cycloaddition of carbonyltriazoles". Chem. Commun. 50, n.º 100 (2014): 15971–74. http://dx.doi.org/10.1039/c4cc08339c.
Texto completoWang, Yan-Yan, Tuan-Jie Wang, Juan Chen, Chao-Yang Wang y Jing Zhu. "Synthesis of Polycationic Aza-Belted Heterocyclic Iodomethane Salts". Advanced Science, Engineering and Medicine 11, n.º 11 (1 de noviembre de 2019): 1134–41. http://dx.doi.org/10.1166/asem.2019.2468.
Texto completoNayl, AbdElAziz A., Ashraf A. Aly, Wael A. A. Arafa, Ismail M. Ahmed, Ahmed I. Abd-Elhamid, Esmail M. El-Fakharany, Mohamed A. Abdelgawad, Hendawy N. Tawfeek y Stefan Bräse. "Azides in the Synthesis of Various Heterocycles". Molecules 27, n.º 12 (9 de junio de 2022): 3716. http://dx.doi.org/10.3390/molecules27123716.
Texto completoBalci, Metin. "Acyl Azides: Versatile Compounds in the Synthesis of Various Heterocycles". Synthesis 50, n.º 07 (1 de febrero de 2018): 1373–401. http://dx.doi.org/10.1055/s-0036-1589527.
Texto completoHeredia-Moya, Jorge, Daniel A. Zurita, José Eduardo Cadena-Cruz y Christian D. Alcívar-León. "Diaza-1,3-butadienes as Useful Intermediate in Heterocycles Synthesis". Molecules 27, n.º 19 (9 de octubre de 2022): 6708. http://dx.doi.org/10.3390/molecules27196708.
Texto completoLystsova, Ekaterina A., Ekaterina E. Khramtsova y Andrey N. Maslivets. "Acyl(imidoyl)ketenes: Reactive Bidentate Oxa/Aza-Dienes for Organic Synthesis". Symmetry 13, n.º 8 (17 de agosto de 2021): 1509. http://dx.doi.org/10.3390/sym13081509.
Texto completoVodnala, Sumathi, Anagani Kanaka Durga Bhavani, Shankaraiah Pagilla, Muralidhar Allam, Nagamani Rayala, Anwita Mudiraj y Phanithi Prakash Babu. "Synthesis and Cytotoxic Studies of Quinazoline-Triazole Hybrid Aza Heterocycles". Russian Journal of General Chemistry 91, n.º 11 (noviembre de 2021): 2304–10. http://dx.doi.org/10.1134/s1070363221110189.
Texto completoKitamura, Mitsuru y Koichi Narasaka. "Synthesis of Aza-Heterocycles from Oximes by Amino-Heck Reaction". Chemical Record 2, n.º 4 (julio de 2002): 268–77. http://dx.doi.org/10.1002/tcr.10030.
Texto completoMa, Shengming. "Heterocycles based on the chemistry of alkylidenecyclopropanes and (aza)-cyclopropenes". Pure and Applied Chemistry 80, n.º 4 (1 de enero de 2008): 695–706. http://dx.doi.org/10.1351/pac200880040695.
Texto completoMajumdar, K. C. y S. K. Samanta. "Studies in aza-Claisen rearrangement: synthesis of dimedone-annelated unusual heterocycles". Tetrahedron 57, n.º 23 (junio de 2001): 4955–58. http://dx.doi.org/10.1016/s0040-4020(01)00405-7.
Texto completoMarini, Francesca, Martina Palomba, Luana Bagnoli y Claudio Santi. "Synthesis of Pyrrolidinols by Radical Additions to Carbonyls Groups". Proceedings 41, n.º 1 (14 de noviembre de 2019): 20. http://dx.doi.org/10.3390/ecsoc-23-06606.
Texto completoRulev, Alexander Yu, Alexey R. Romanov, Alexander V. Popov, Evgeniy V. Kondrashov y Sergey V. Zinchenko. "Reaction of Bromoenones with Amidines: A Simple Catalyst-Free Approach to Trifluoromethylated Pyrimidines". Synthesis 52, n.º 10 (9 de marzo de 2020): 1512–22. http://dx.doi.org/10.1055/s-0040-1707969.
Texto completoPinho e Melo, Teresa M. V. D. "Chemistry of aza- and diazafulvenium methides in heterocyclic synthesis". Pure and Applied Chemistry 88, n.º 5 (1 de mayo de 2016): 457–75. http://dx.doi.org/10.1515/pac-2016-0404.
Texto completoCherkasov, V. M. y N. A. Kapran. "Aza-1,3-butadienes in synthesis of nitrogen-containing six-membered heterocycles (review)". Chemistry of Heterocyclic Compounds 28, n.º 10 (octubre de 1992): 1101–8. http://dx.doi.org/10.1007/bf00529568.
Texto completoLlona-Minguez, Sabin, Matthieu Desroses, Artin Ghassemian, Sylvain A. Jacques, Lars Eriksson, Rebecka Isacksson, Tobias Koolmeister, Pål Stenmark, Martin Scobie y Thomas Helleday. "Vinylic MIDA Boronates: New Building Blocks for the Synthesis of Aza-Heterocycles". Chemistry - A European Journal 21, n.º 20 (25 de marzo de 2015): 7394–98. http://dx.doi.org/10.1002/chem.201406549.
Texto completoGeng, Zhi-Cong, Jian Chen, Ning Li, Xiao-Fei Huang, Yong Zhang, Ya-Wen Zhang y Xing-Wang Wang. "Organocatalytic cascade aza-Michael/hemiacetal reaction between disubstituted hydrazines and α,β-unsaturated aldehydes: Highly diastereo- and enantioselective synthesis of pyrazolidine derivatives". Beilstein Journal of Organic Chemistry 8 (9 de octubre de 2012): 1710–20. http://dx.doi.org/10.3762/bjoc.8.195.
Texto completoFustero, Santos, María Sánchez-Roselló y Carlos del Pozo. "Asymmetric tandem reactions: New synthetic strategies". Pure and Applied Chemistry 82, n.º 3 (18 de febrero de 2010): 669–77. http://dx.doi.org/10.1351/pac-con-09-09-07.
Texto completoVinogradov, Maxim G., Olga V. Turova y Sergei G. Zlotin. "Recent advances in the asymmetric synthesis of pharmacology-relevant nitrogen heterocycles via stereoselective aza-Michael reactions". Organic & Biomolecular Chemistry 17, n.º 15 (2019): 3670–708. http://dx.doi.org/10.1039/c8ob03034k.
Texto completoEl Bouakher, Abderrahman, Arnaud Martel y Sébastien Comesse. "α-Halogenoacetamides: versatile and efficient tools for the synthesis of complex aza-heterocycles". Organic & Biomolecular Chemistry 17, n.º 37 (2019): 8467–85. http://dx.doi.org/10.1039/c9ob01683j.
Texto completoSingh, Surjeet, Ranjay Shaw, Shally, Sandeep Chaudhary, Abhinav Kumar y Ramendra Pratap. "Synthesis of arylated and aminated naphthalenes and their synthetic applications for aza-heterocycles". Tetrahedron 72, n.º 41 (octubre de 2016): 6436–43. http://dx.doi.org/10.1016/j.tet.2016.08.044.
Texto completoTimmer, Mattie S. M., Martijn D. P. Risseeuw, Martijn Verdoes, Dmitri V. Filippov, Jasper R. Plaisier, Gijsbert A. van der Marel, Herman S. Overkleeft y Jacques H. van Boom. "Synthesis of functionalized heterocycles via a tandem Staudinger/aza-Wittig/Ugi multicomponent reaction". Tetrahedron: Asymmetry 16, n.º 1 (enero de 2005): 177–85. http://dx.doi.org/10.1016/j.tetasy.2004.11.079.
Texto completoBurgin, Ryan N., Simon Jones y B. Tarbit. "Scope and limitations of the Minisci reaction for the synthesis of aza-heterocycles". Tetrahedron Letters 50, n.º 49 (diciembre de 2009): 6772–74. http://dx.doi.org/10.1016/j.tetlet.2009.09.112.
Texto completoWhelligan, Daniel K., Douglas W. Thomson, Dawn Taylor y Swen Hoelder. "Two-Step Synthesis of Aza- and Diazaindoles from Chloroamino-N-heterocycles Using Ethoxyvinylborolane". Journal of Organic Chemistry 75, n.º 1 (enero de 2010): 11–15. http://dx.doi.org/10.1021/jo902143f.
Texto completoLugiņina, Jevgeņija y Māris Turks. "Non-activated aziridines as building blocks for the synthesis of aza-heterocycles (microreview)". Chemistry of Heterocyclic Compounds 52, n.º 10 (octubre de 2016): 773–75. http://dx.doi.org/10.1007/s10593-016-1962-z.
Texto completoEl-Ebiary, N. M., R. H. Swellem y G. A. M. Nawwar. "Design, Synthesis and Anticancer Activity of Aza Heterocycles Containing Gallate Moiety (Part III)". Pharmaceutical Chemistry Journal 51, n.º 1 (abril de 2017): 39–48. http://dx.doi.org/10.1007/s11094-017-1554-y.
Texto completoMajumdar, K. C. y S. K. Samanta. "ChemInform Abstract: Studies in Aza-Claisen Rearrangement: Synthesis of Dimedone-Anellated Unusual Heterocycles." ChemInform 32, n.º 37 (24 de mayo de 2010): no. http://dx.doi.org/10.1002/chin.200137055.
Texto completoAlbenque-Rubio, Sandra, Jean Guillon, Anita Cohen, Patrice Agnamey, Solène Savrimoutou, Stéphane Moreau, Jean-Louis Mergny et al. "Synthesis and Antimalarial Evaluation of New 1,3,5-tris[(4-(Substituted-aminomethyl)phenyl)methyl]benzene Derivatives: A Novel Alternative Antiparasitic Scaffold". Drugs and Drug Candidates 2, n.º 3 (8 de agosto de 2023): 653–72. http://dx.doi.org/10.3390/ddc2030033.
Texto completoAdda, Abdelghani y Hayat Sediki. "Theoretical Study of the Aza˗Wittig Reaction, Me3P=NR (R = Methyl or Phenyl) with Aldehyde Using the DFT and DFT-D Methods (Dispersion Correction)". Chemistry Proceedings 3, n.º 1 (14 de noviembre de 2020): 47. http://dx.doi.org/10.3390/ecsoc-24-08349.
Texto completoRenslo, Adam R., Hongwu Gao, Priyadarshini Jaishankar, Revathy Venkatachalam y Mikhail F. Gordeev. "Synthesis of Aza-, Oxa-, and Thiabicyclo[3.1.0]hexane Heterocycles from a Common Synthetic Intermediate". Organic Letters 7, n.º 13 (junio de 2005): 2627–30. http://dx.doi.org/10.1021/ol050730h.
Texto completoOlier, Clarisse, Mustapha Kaafarani, Stéphane Gastaldi y Michèle P. Bertrand. "Synthesis of tetrahydropyrans and related heterocycles via prins cyclization; extension to aza-prins cyclization". Tetrahedron 66, n.º 2 (enero de 2010): 413–45. http://dx.doi.org/10.1016/j.tet.2009.10.069.
Texto completoCHERKASOV, V. M. y N. A. KAPRAN. "ChemInform Abstract: Aza-1,3-butadienes in the Synthesis of Nitrogen-Containing 6-Membered Heterocycles". ChemInform 24, n.º 44 (20 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199344323.
Texto completoLlona-Minguez, Sabin, Matthieu Desroses, Artin Ghassemian, Sylvain A. Jacques, Lars Eriksson, Rebecka Isacksson, Tobias Koolmeister, Paal Stenmark, Martin Scobie y Thomas Helleday. "ChemInform Abstract: Vinylic MIDA Boronates: New Building Blocks for the Synthesis of Aza-Heterocycles." ChemInform 46, n.º 40 (17 de septiembre de 2015): no. http://dx.doi.org/10.1002/chin.201540135.
Texto completoPrishchenko, Andrey A., Roman S. Alekseyev, Mikhail V. Livantsov, Olga P. Novikova, Ludmila I. Livantsova, Vladimir I. Terenin y Valery S. Petrosyan. "Synthesis of new functionalized mono- and diphosphonic acids with five-membered aza-heterocycles moieties". Heteroatom Chemistry 28, n.º 1 (13 de diciembre de 2016): e21353. http://dx.doi.org/10.1002/hc.21353.
Texto completoRace, Nicholas J., Ian R. Hazelden, Adele Faulkner y John F. Bower. "Recent developments in the use of aza-Heck cyclizations for the synthesis of chiral N-heterocycles". Chemical Science 8, n.º 8 (2017): 5248–60. http://dx.doi.org/10.1039/c7sc01480e.
Texto completoRostovskii, Nikolai V., Mikhail S. Novikov y Alexander F. Khlebnikov. "Electrocyclizations of Conjugated Azapolyenes Produced in Reactions of Azaheterocycles with Metal Carbenes". Organics 2, n.º 3 (14 de septiembre de 2021): 313–36. http://dx.doi.org/10.3390/org2030017.
Texto completoNarasaka, K. "Synthesis of azaheterocycles from oxime derivatives". Pure and Applied Chemistry 75, n.º 1 (1 de enero de 2003): 19–28. http://dx.doi.org/10.1351/pac200375010019.
Texto completoMagoo, D., Komal Aggarwal, Shruti Gupta y Kalawati Meena. "Enamines and their variants as intermediates for synthesis of aza-heterocycles with applications in MCRs". Tetrahedron 103 (enero de 2022): 132545. http://dx.doi.org/10.1016/j.tet.2021.132545.
Texto completoTakizawa, Shinobu. "Organocatalytic Synthesis of Highly Functionalized Heterocycles by Enantioselective aza-Morita–Baylis–Hillman-Type Domino Reactions". Chemical and Pharmaceutical Bulletin 68, n.º 4 (1 de abril de 2020): 299–315. http://dx.doi.org/10.1248/cpb.c19-00900.
Texto completoWu, Jiajun y Christophe Darcel. "Iron-Catalyzed Hydrogen Transfer Reduction of Nitroarenes with Alcohols: Synthesis of Imines and Aza Heterocycles". Journal of Organic Chemistry 86, n.º 1 (16 de diciembre de 2020): 1023–36. http://dx.doi.org/10.1021/acs.joc.0c02505.
Texto completoEguchi, Shoji, Takashi Okano y Tomohiro Okawa. "ChemInform Abstract: Synthesis of Heterocyclic Natural Products and Related Heterocycles by the Aza-Wittig Methodology". ChemInform 30, n.º 27 (15 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199927287.
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