Статті в журналах з теми "Carbon-hetero bond transformation reactions"
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Valdés, Carlos, Raquel Barroso, and María Cabal. "Pd-catalyzed Auto-Tandem Cascades Based on N-Sulfonylhydrazones: Hetero- and Carbocyclization Processes." Synthesis 28, no. 19 (August 10, 2017): 4434–47. http://dx.doi.org/10.1055/s-0036-1588535.
Повний текст джерелаRai, Vijai K., Fooleswar Verma, Suhasini Mahata, Smita R. Bhardiya, Manorama Singh, and Ankita Rai. "Metal Doped-C3N4/Fe2O4: Efficient and Versatile Heterogenous Catalysts for Organic Transformations." Current Organic Chemistry 23, no. 12 (September 20, 2019): 1284–306. http://dx.doi.org/10.2174/1385272823666190709113758.
Повний текст джерелаTietze, L. F., and N. Rackelmann. "Domino reactions in the synthesis of heterocyclic natural products and analogs." Pure and Applied Chemistry 76, no. 11 (January 1, 2004): 1967–83. http://dx.doi.org/10.1351/pac200476111967.
Повний текст джерелаSmaligo, Andrew J., Manisha Swain, Jason C. Quintana, Mikayla F. Tan, Danielle A. Kim, and Ohyun Kwon. "Hydrodealkenylative C(sp3)–C(sp2) bond fragmentation." Science 364, no. 6441 (May 16, 2019): 681–85. http://dx.doi.org/10.1126/science.aaw4212.
Повний текст джерелаPoursharif, Akram, Mahmood Kazemzad, and Nooshin Salman Tabrizi. "Fabrication of Carbon Nanotube Granules as Pd Catalyst Supports for Hydrogenation of Carbon-Carbon Triple Bond." Advanced Materials Research 829 (November 2013): 82–85. http://dx.doi.org/10.4028/www.scientific.net/amr.829.82.
Повний текст джерелаKumar, Sumit, and Kishor Padala. "The recent advances in K2S2O8-mediated cyclization/coupling reactions via an oxidative transformation." Chemical Communications 56, no. 96 (2020): 15101–17. http://dx.doi.org/10.1039/d0cc06036d.
Повний текст джерелаLiu, Leping, Bo Xu, and Gerald B. Hammond. "Construction of cyclic enones via gold-catalyzed oxygen transfer reactions." Beilstein Journal of Organic Chemistry 7 (May 13, 2011): 606–14. http://dx.doi.org/10.3762/bjoc.7.71.
Повний текст джерелаCho, Inha, Zhi-Jun Jia, and Frances H. Arnold. "Site-selective enzymatic C‒H amidation for synthesis of diverse lactams." Science 364, no. 6440 (May 9, 2019): 575–78. http://dx.doi.org/10.1126/science.aaw9068.
Повний текст джерелаQuan, Zheng-Jun, Xi-Cun Wang, Ming-Xia Liu, and Hai-Peng Gong. "Palladium-Catalyzed Copper-Promoted Hiyama-Type Carbon–Carbon Cross-Coupling Reactions of Dihetaryl Disulfides as Electrophiles." Synlett 29, no. 03 (October 26, 2017): 330–35. http://dx.doi.org/10.1055/s-0036-1589116.
Повний текст джерелаYang, Qiaoyu, Xiaoxian Guo, Yuwan Liu, and Huifeng Jiang. "Biocatalytic C-C Bond Formation for One Carbon Resource Utilization." International Journal of Molecular Sciences 22, no. 4 (February 14, 2021): 1890. http://dx.doi.org/10.3390/ijms22041890.
Повний текст джерелаHeravi, Majid M., Mahzad Dehghani, Vahideh Zadsirjan, and Manijheh Ghanbarian. "Alkynes as Privileged Synthons in Selected Organic Name Reactions." Current Organic Synthesis 16, no. 2 (March 26, 2019): 205–43. http://dx.doi.org/10.2174/1570179416666190126100744.
Повний текст джерелаFujihara, Tetsuaki, and Yasushi Tsuji. "Cobalt- and rhodium-catalyzed carboxylation using carbon dioxide as the C1 source." Beilstein Journal of Organic Chemistry 14 (September 19, 2018): 2435–60. http://dx.doi.org/10.3762/bjoc.14.221.
Повний текст джерелаTsuji, Yasushi, and Tetsuaki Fujihara. "Carbon dioxide as a carbon source in organic transformation: carbon–carbon bond forming reactions by transition-metal catalysts." Chemical Communications 48, no. 80 (2012): 9956. http://dx.doi.org/10.1039/c2cc33848c.
Повний текст джерелаGuo, Fenghai, Jayla A. Young, Mina S. Perez, Holden A. Hankerson, and Alex M. Chavez. "Progress on the Cu-Catalyzed 1,4-Conjugate Addition to Thiochromones." Catalysts 13, no. 4 (April 8, 2023): 713. http://dx.doi.org/10.3390/catal13040713.
Повний текст джерелаChinkov, Nicka, G. Sklute, Helena Chechik, Adi Abramovitch, Deborah Amsallem, J. Varghese, Swapan Majumdar, and I. Marek. "New regio-, stereo-, diastereo- and enantioselective one-pot reactions mediated by organometallic derivatives." Pure and Applied Chemistry 76, no. 3 (January 1, 2004): 517–35. http://dx.doi.org/10.1351/pac200476030517.
Повний текст джерелаPrasanna, Pitchaimani, Pethaiah Gunasekaran, Subbu Perumal, and J. Carlos Menéndez. "A catalyst-free multicomponent domino sequence for the diastereoselective synthesis of (E)-3-[2-arylcarbonyl-3-(arylamino)allyl]chromen-4-ones." Beilstein Journal of Organic Chemistry 10 (February 21, 2014): 459–65. http://dx.doi.org/10.3762/bjoc.10.43.
Повний текст джерелаTsuji, Yasushi, and Tetsuaki Fujihara. "ChemInform Abstract: Carbon Dioxide as a Carbon Source in Organic Transformation: Carbon-Carbon Bond Forming Reactions by Transition-Metal Catalysts." ChemInform 43, no. 50 (November 29, 2012): no. http://dx.doi.org/10.1002/chin.201250235.
Повний текст джерелаPires, Marina, Sara Purificação, A. Santos, and M. Marques. "The Role of PEG on Pd- and Cu-Catalyzed Cross-Coupling Reactions." Synthesis 49, no. 11 (April 26, 2017): 2337–50. http://dx.doi.org/10.1055/s-0036-1589498.
Повний текст джерелаPagar, Vinayak Vishnu, and T. V. RajanBabu. "Tandem catalysis for asymmetric coupling of ethylene and enynes to functionalized cyclobutanes." Science 361, no. 6397 (July 5, 2018): 68–72. http://dx.doi.org/10.1126/science.aat6205.
Повний текст джерелаChatterjee, Rupak, and Asim Bhaumik. "Carboxylation of Alkenes and Alkynes Using CO2 as a Reagent: An Overview." Current Organic Chemistry 26, no. 1 (January 2022): 60–70. http://dx.doi.org/10.2174/1385272825666211206090621.
Повний текст джерелаLiu, Wei-Bing, Cui Chen, Qing Zhang, and Zhi-Bo Zhu. "Organic synthesis using (diacetoxyiodo)benzene (DIB): Unexpected and novel oxidation of 3-oxo-butanamides to 2,2-dihalo-N-phenylacetamides." Beilstein Journal of Organic Chemistry 8 (March 7, 2012): 344–48. http://dx.doi.org/10.3762/bjoc.8.38.
Повний текст джерелаLv, Ze-Jie, Junnian Wei, Wen-Xiong Zhang, Ping Chen, Dehui Deng, Zhang-Jie Shi, and Zhenfeng Xi. "Direct transformation of dinitrogen: synthesis of N-containing organic compounds via N−C bond formation." National Science Review 7, no. 10 (June 23, 2020): 1564–83. http://dx.doi.org/10.1093/nsr/nwaa142.
Повний текст джерелаKumagai, Naoya, and Masakatsu Shibasaki. "7-Azaindoline Auxiliary: A Versatile Attachment Facilitating Enantioselective C–C Bond-Forming Catalysis." Synthesis 51, no. 01 (November 30, 2018): 185–93. http://dx.doi.org/10.1055/s-0037-1610412.
Повний текст джерелаObydennov, Dmitrii L., Vyacheslav D. Steben’kov, Konstantin L. Obydennov, Sergey A. Usachev, Vladimir S. Moshkin, and Vyacheslav Y. Sosnovskikh. "Reactions of 4-Pyrones with Azomethine Ylides as a Chemoselective Method for the Construction of Multisubstituted Pyrano[2,3-c]pyrrolidines." Synthesis 53, no. 15 (April 13, 2021): 2621–31. http://dx.doi.org/10.1055/s-0040-1706032.
Повний текст джерелаHölscher, Markus, Christoph Gürtler, Wilhelm Keim, Thomas E. Müller, Martina Peters, and Walter Leitner. "Carbon Dioxide as a Carbon Resource – Recent Trends and Perspectives." Zeitschrift für Naturforschung B 67, no. 10 (October 1, 2012): 961–75. http://dx.doi.org/10.5560/znb.2012-0219.
Повний текст джерелаKim, Yohan, Seongmin Kim, Minyoung Shim, Yusik Oh, Kug-Seung Lee, Yousung Jung, and Hye Ryung Byon. "Alteration of Oxygen Evolution Mechanisms in Layered LiCoO2 Structures By Intercalation of Alkali Metal Ions." ECS Meeting Abstracts MA2022-01, no. 34 (July 7, 2022): 1356. http://dx.doi.org/10.1149/ma2022-01341356mtgabs.
Повний текст джерелаKannath, Suraj, Paweł Adamczyk, Langping Wu, Hans H. Richnow та Agnieszka Dybala-Defratyka. "Can Alkaline Hydrolysis of γ-HCH Serve as a Model Reaction to Study Its Aerobic Enzymatic Dehydrochlorination by LinA?" International Journal of Molecular Sciences 20, № 23 (26 листопада 2019): 5955. http://dx.doi.org/10.3390/ijms20235955.
Повний текст джерелаAkiba, Ikumi, Naoki Shida, and Mahito Atobe. "Oxidative C-F Bonds Activation Using Electrochemical Techniques." ECS Meeting Abstracts MA2023-02, no. 52 (December 22, 2023): 2487. http://dx.doi.org/10.1149/ma2023-02522487mtgabs.
Повний текст джерелаKiss, Loránd, Márton Kardos, Csaba Vass та Ferenc Fülöp. "Application of Metathesis Reactions in the Synthesis and Transformations of Functionalized β-Amino Acid Derivatives". Synthesis 50, № 18 (26 липня 2018): 3571–88. http://dx.doi.org/10.1055/s-0036-1591600.
Повний текст джерелаBalci, Metin. "Acyl Azides: Versatile Compounds in the Synthesis of Various Heterocycles." Synthesis 50, no. 07 (February 1, 2018): 1373–401. http://dx.doi.org/10.1055/s-0036-1589527.
Повний текст джерелаKim, Taeho, Peter J. Stogios, Anna N. Khusnutdinova, Kayla Nemr, Tatiana Skarina, Robert Flick, Jeong Chan Joo, Radhakrishnan Mahadevan, Alexei Savchenko, and Alexander F. Yakunin. "Rational engineering of 2-deoxyribose-5-phosphate aldolases for the biosynthesis of (R)-1,3-butanediol." Journal of Biological Chemistry 295, no. 2 (December 5, 2019): 597–609. http://dx.doi.org/10.1074/jbc.ra119.011363.
Повний текст джерелаBarata-Vallejo, Sebastián, and Al Postigo. "Photocatalytic Difluoromethylation Reactions of Aromatic Compounds and Aliphatic Multiple C–C Bonds." Molecules 24, no. 24 (December 6, 2019): 4483. http://dx.doi.org/10.3390/molecules24244483.
Повний текст джерелаLumb, Jean-Philip, and Kenneth Esguerra. "Cu(III)-Mediated Aerobic Oxidations." Synthesis 51, no. 02 (December 3, 2018): 334–58. http://dx.doi.org/10.1055/s-0037-1609635.
Повний текст джерелаMartin, Nelson, and Ruchi Bharti. "Arynes in Natural Product Synthesis." International Journal for Research in Applied Science and Engineering Technology 11, no. 4 (April 30, 2023): 2633–44. http://dx.doi.org/10.22214/ijraset.2023.50703.
Повний текст джерелаDeng, Yu-Hua, Zhihui Shao, and Hui Wang. "An Update of N-Tosylhydrazones: Versatile Reagents for Metal-Catalyzed and Metal-Free Coupling Reactions." Synthesis 50, no. 12 (May 23, 2018): 2281–306. http://dx.doi.org/10.1055/s-0036-1591993.
Повний текст джерелаCherkas, Andrew A., Nasim Hadj-Bagheri, Arthur J. Carty, Enrico Sappa, Maria Angela Pellinghelli, and Antonio Tiripicchio. "Polynuclear acetylide chemistry: acetylide to acetylene transformation at a binuclear center via carbon-carbon and carbon-nitrogen bond-forming reactions. X-ray structure of Os2(CO)6[.mu.-.eta.2-.dblvert.-C[C(NHBu-tert)(NEt2)]CPh](.mu.-PPh2)." Organometallics 9, no. 6 (June 1990): 1887–92. http://dx.doi.org/10.1021/om00156a031.
Повний текст джерелаGrossi, Vincent, Cristiana Cravo-Laureau, Alain Méou, Danielle Raphel, Frédéric Garzino, and Agnès Hirschler-Réa. "Anaerobic 1-Alkene Metabolism by the Alkane- and Alkene-Degrading Sulfate Reducer Desulfatibacillum aliphaticivorans Strain CV2803T." Applied and Environmental Microbiology 73, no. 24 (October 26, 2007): 7882–90. http://dx.doi.org/10.1128/aem.01097-07.
Повний текст джерелаMajee, Suman, Devalina Ray, and Bimal KrishnaBanik. "Samarium-Mediated Asymmetric Synthesis." Catalysts 13, no. 1 (December 24, 2022): 24. http://dx.doi.org/10.3390/catal13010024.
Повний текст джерелаSarabia, Francisco, and Iván Cheng-Sánchez. "Recent Advances in Total Synthesis via Metathesis Reactions." Synthesis 50, no. 19 (July 18, 2018): 3749–86. http://dx.doi.org/10.1055/s-0037-1610206.
Повний текст джерелаKataria, Meenal, Subhamay Pramanik, Navleen Kaur, Manoj Kumar та Vandana Bhalla. "Ferromagnetic α-Fe2O3 NPs: a potential catalyst in Sonogashira–Hagihara cross coupling and hetero-Diels–Alder reactions". Green Chemistry 18, № 6 (2016): 1495–505. http://dx.doi.org/10.1039/c5gc02337h.
Повний текст джерелаMenon, Rajeev S., Akkattu T. Biju, and Vijay Nair. "Recent advances in N-heterocyclic carbene (NHC)-catalysed benzoin reactions." Beilstein Journal of Organic Chemistry 12 (March 9, 2016): 444–61. http://dx.doi.org/10.3762/bjoc.12.47.
Повний текст джерелаLi, Fang, W. Felix Zhu, Claire Empel, Oleksandr Datsenko, Adarsh Kumar, Yameng Xu, Johanna H. M. Ehrler, et al. "Photosensitization enables Pauson-Khand–type reactions with nitrenes." Science 383, no. 6682 (February 2, 2024): 498–503. http://dx.doi.org/10.1126/science.adm8095.
Повний текст джерелаPuzanov, Andrey I., Dmitry S. Ryabukhin, Anna S. Zalivatskaya, Dmitriy N. Zakusilo, Darya S. Mikson, Irina A. Boyarskaya, and Aleksander V. Vasilyev. "Synthesis of 5-arylacetylenyl-1,2,4-oxadiazoles and their transformations under superelectrophilic activation conditions." Beilstein Journal of Organic Chemistry 17 (September 15, 2021): 2417–24. http://dx.doi.org/10.3762/bjoc.17.158.
Повний текст джерелаGu, Huoliang, Xiong Sun, Yong Wang, Haihong Wu, and Peng Wu. "Highly efficient mesoporous polymer supported phosphine-gold(i) complex catalysts for amination of allylic alcohols and intramolecular cyclization reactions." RSC Advances 8, no. 4 (2018): 1737–43. http://dx.doi.org/10.1039/c7ra12498h.
Повний текст джерелаCoates, Greg, Feriel Rekhroukh, and Mark R. Crimmin. "Breaking Carbon–Fluorine Bonds with Main Group Nucleophiles." Synlett 30, no. 20 (November 12, 2019): 2233–46. http://dx.doi.org/10.1055/s-0039-1690738.
Повний текст джерелаSala, Roberto, Camilla Loro, Francesca Foschi, and Gianluigi Broggini. "Transition Metal Catalyzed Azidation Reactions." Catalysts 10, no. 10 (October 12, 2020): 1173. http://dx.doi.org/10.3390/catal10101173.
Повний текст джерелаQuiclet-Sire, Béatrice, and Samir Z. Zard. "Some aspects of radical cascade and relay reactions." Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences 473, no. 2200 (April 2017): 20160859. http://dx.doi.org/10.1098/rspa.2016.0859.
Повний текст джерелаConstantino, Andre F., Carla S. Francisco, Diana C. Cubides-Roman, and Valdemar Lacerda. "Hetero-Diels-Alder Reactions in the Synthesis of Biologically Active Nitrogen Compounds: A Review." Current Organic Synthesis 15, no. 1 (March 20, 2018): 84–104. http://dx.doi.org/10.2174/1570179414666170517170230.
Повний текст джерелаBrahmachari, Goutam, Nayana Nayek, Mullicka Mandal, Anindita Bhowmick, and Indrajit Karmakar. "Ultrasound-promoted Organic Synthesis - A Recent Update." Current Organic Chemistry 25, no. 13 (September 2, 2021): 1539–65. http://dx.doi.org/10.2174/1385272825666210316122319.
Повний текст джерелаGlover, Stephen A., Arvi Rauk, Jeanne M. Buccigross, John J. Campbell, Gerard P. Hammond, Guoning Mo, Luke E. Andrews, and Ashley-Mae E. Gillson. "The HERON reaction Origin, theoretical background, and prevalence." Canadian Journal of Chemistry 83, no. 9 (September 1, 2005): 1492–509. http://dx.doi.org/10.1139/v05-150.
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