Zeitschriftenartikel zum Thema „Amides“
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Soong, Chee-Leong, Jun Ogawa und Sakayu Shimizu. „A Novel Amidase (Half-Amidase) for Half-Amide Hydrolysis Involved in the Bacterial Metabolism of Cyclic Imides“. Applied and Environmental Microbiology 66, Nr. 5 (01.05.2000): 1947–52. http://dx.doi.org/10.1128/aem.66.5.1947-1952.2000.
Barham, Joshua P., und Jaspreet Kaur. „Site-Selective C(sp3)–H Functionalizations Mediated by Hydrogen Atom Transfer Reactions via α-Amino/α-Amido Radicals“. Synthesis 54, Nr. 06 (25.10.2021): 1461–77. http://dx.doi.org/10.1055/a-1677-6619.
Zhou, Yongyun, Ruhima Khan, Baomin Fan und Lijin Xu. „Ruthenium-Catalyzed Selective Reduction of Carboxylic Esters and Carboxamides“. Synthesis 51, Nr. 12 (30.04.2019): 2491–505. http://dx.doi.org/10.1055/s-0037-1611524.
Zarecki, Adam P., Jacek L. Kolanowski und Wojciech T. Markiewicz. „Microwave-Assisted Catalytic Method for a Green Synthesis of Amides Directly from Amines and Carboxylic Acids“. Molecules 25, Nr. 8 (11.04.2020): 1761. http://dx.doi.org/10.3390/molecules25081761.
Orsy, György, Sayeh Shahmohammadi und Enikő Forró. „A Sustainable Green Enzymatic Method for Amide Bond Formation“. Molecules 28, Nr. 15 (28.07.2023): 5706. http://dx.doi.org/10.3390/molecules28155706.
Martinez-Rodríguez, Sergio, Rafael Contreras-Montoya, Jesús M. Torres, Luis Álvarez de Cienfuegos und Jose Antonio Gavira. „A New L-Proline Amide Hydrolase with Potential Application within the Amidase Process“. Crystals 12, Nr. 1 (23.12.2021): 18. http://dx.doi.org/10.3390/cryst12010018.
Khalimon, Andrey, Kristina Gudun und Davit Hayrapetyan. „Base Metal Catalysts for Deoxygenative Reduction of Amides to Amines“. Catalysts 9, Nr. 6 (28.05.2019): 490. http://dx.doi.org/10.3390/catal9060490.
Fournand, David, Frederic Bigey und Alain Arnaud. „Acyl Transfer Activity of an Amidase from Rhodococcussp. Strain R312: Formation of a Wide Range of Hydroxamic Acids“. Applied and Environmental Microbiology 64, Nr. 8 (01.08.1998): 2844–52. http://dx.doi.org/10.1128/aem.64.8.2844-2852.1998.
Ding, Wen, Shaoyu Mai und Qiuling Song. „Molecular-oxygen-promoted Cu-catalyzed oxidative direct amidation of nonactivated carboxylic acids with azoles“. Beilstein Journal of Organic Chemistry 11 (11.11.2015): 2158–65. http://dx.doi.org/10.3762/bjoc.11.233.
Meerakrishna, Ramakrishnan Suseela, und Ponnusamy Shanmugam. „Synthesis of blue-red emissive amido-substituted di(het)aryl and tri(het)aryl amine derivatives via chemoselective N-mono and N,N-diarylation of (het) aryl amino amides using benzyne/arynes“. New Journal of Chemistry 43, Nr. 6 (2019): 2550–58. http://dx.doi.org/10.1039/c8nj05823g.
Krieck, Sven, Philipp Schüler, Jan Peschel und Matthias Westerhausen. „Straightforward One-Pot Syntheses of Silylamides of Magnesium and Calcium via an In Situ Grignard Metalation Method“. Synthesis 51, Nr. 05 (13.12.2018): 1115–22. http://dx.doi.org/10.1055/s-0037-1610407.
Selvakumar, Kumaravel, Kesamreddy Rangareddy und John F. Harrod. „The titanocene-catalyzed reduction of acetamides to tertiary amines by PhMeSiH2“. Canadian Journal of Chemistry 82, Nr. 8 (01.08.2004): 1244–48. http://dx.doi.org/10.1139/v04-063.
Yao, Lei, Ming-Yi Wang, Xin-Ke Wang, Yi-Jun Liu, Hang-Fei Chen, Jun Zheng, Wei Nie et al. „Detection of atmospheric gaseous amines and amides by a high-resolution time-of-flight chemical ionization mass spectrometer with protonated ethanol reagent ions“. Atmospheric Chemistry and Physics 16, Nr. 22 (23.11.2016): 14527–43. http://dx.doi.org/10.5194/acp-16-14527-2016.
Khaldoun, Khadidja, Abdelmounaim Safer, Salima Saidi-Besbes, Bertrand Carboni, Rémy Le Guével und François Carreaux. „An Efficient Solvent-Free Microwave-Assisted Synthesis of Cinnamamides by Amidation Reaction Using Phenylboronic Acid/Lewis Base Co-catalytic System“. Synthesis 51, Nr. 20 (29.07.2019): 3891–900. http://dx.doi.org/10.1055/s-0039-1690132.
Trott, Sandra, Sibylle Bürger, Carsten Calaminus und Andreas Stolz. „Cloning and Heterologous Expression of an Enantioselective Amidase from Rhodococcus erythropolis Strain MP50“. Applied and Environmental Microbiology 68, Nr. 7 (Juli 2002): 3279–86. http://dx.doi.org/10.1128/aem.68.7.3279-3286.2002.
Šilhánková, Alexandra, Karel Šindelář, Karel Dobrovský, Ivan Krejčí, Jarmila Hodková und Zdeněk Polívka. „Synthesis of New L-Proline Amides with Anticonvulsive Effect“. Collection of Czechoslovak Chemical Communications 61, Nr. 7 (1996): 1085–92. http://dx.doi.org/10.1135/cccc19961085.
Haake, Paul, und Donald A. Tyssee. „Estimation of Charge Density on Nitrogen in Amides by Measurement of One-Bond Carbon-Hydrogen Nuclear Coupling Constants in N-CH3 Group“. Zeitschrift für Naturforschung A 48, Nr. 1-2 (01.02.1993): 58–62. http://dx.doi.org/10.1515/zna-1993-1-216.
Qu, Jing, Shishan Yu, Wenzhao Tang, Yunbao Liu, Yue Liu und Jing Liu. „Progress on Cassaine-Type Diterpenoid Ester Amines and Amides (Erythrophleum Alkaloids)“. Natural Product Communications 1, Nr. 10 (Oktober 2006): 1934578X0600101. http://dx.doi.org/10.1177/1934578x0600101005.
Zahardis, J., S. Geddes und G. A. Petrucci. „The ozonolysis of primary aliphatic amines in single and multicomponent fine particles“. Atmospheric Chemistry and Physics Discussions 7, Nr. 5 (15.10.2007): 14603–38. http://dx.doi.org/10.5194/acpd-7-14603-2007.
Zahardis, J., S. Geddes und G. A. Petrucci. „The ozonolysis of primary aliphatic amines in fine particles“. Atmospheric Chemistry and Physics 8, Nr. 5 (29.02.2008): 1181–94. http://dx.doi.org/10.5194/acp-8-1181-2008.
Waseem Abbasi, Sana, Naveed Zafar Ali, Martin Etter, Muhammad Shabbir, Zareen Akhter, Stacey J. Smith, Hammad Ismail und Bushra Mirza. „Synthesis, Characterization and Biological Studies of Ether–Based Ferrocenyl Amides and their Organic Analogues“. Crystals 10, Nr. 6 (04.06.2020): 480. http://dx.doi.org/10.3390/cryst10060480.
Dunn, P., E. A. Parkes und J. B. Polya. „Amides IX: Acylation of amides and amines“. Recueil des Travaux Chimiques des Pays-Bas 71, Nr. 7 (02.09.2010): 676–83. http://dx.doi.org/10.1002/recl.19520710708.
Sonke, Theo, Sandra Ernste, Renate F. Tandler, Bernard Kaptein, Wilco P. H. Peeters, Friso B. J. van Assema, Marcel G. Wubbolts und Hans E. Schoemaker. „l-Selective Amidase with Extremely Broad Substrate Specificity from Ochrobactrum anthropi NCIMB 40321“. Applied and Environmental Microbiology 71, Nr. 12 (Dezember 2005): 7961–73. http://dx.doi.org/10.1128/aem.71.12.7961-7973.2005.
North, Michael. „Amines and amides“. Journal of the Chemical Society, Perkin Transactions 1, Nr. 16 (1999): 2209–29. http://dx.doi.org/10.1039/a903369f.
North, Michael. „Amines and amides“. Contemporary Organic Synthesis 1, Nr. 6 (1994): 475. http://dx.doi.org/10.1039/co9940100475.
North, Michael. „Amines and amides“. Contemporary Organic Synthesis 2, Nr. 4 (1995): 269. http://dx.doi.org/10.1039/co9950200269.
North, Michael. „Amines and amides“. Contemporary Organic Synthesis 3, Nr. 4 (1996): 323. http://dx.doi.org/10.1039/co9960300323.
North, Michael. „Amines and amides“. Contemporary Organic Synthesis 4, Nr. 4 (1997): 326. http://dx.doi.org/10.1039/co9970400326.
North, Michael. „Amines and amides“. Journal of the Chemical Society, Perkin Transactions 1, Nr. 17 (1998): 2959–72. http://dx.doi.org/10.1039/a802125b.
Xu, Qing, Huamei Xie, Er-Lei Zhang, Xiantao Ma, Jianhui Chen, Xiao-Chun Yu und Huan Li. „Selective catalytic Hofmann N-alkylation of poor nucleophilic amines and amides with catalytic amounts of alkyl halides“. Green Chemistry 18, Nr. 14 (2016): 3940–44. http://dx.doi.org/10.1039/c6gc00938g.
Kumagai, Naoya, und Masakatsu Shibasaki. „7-Azaindoline Auxiliary: A Versatile Attachment Facilitating Enantioselective C–C Bond-Forming Catalysis“. Synthesis 51, Nr. 01 (30.11.2018): 185–93. http://dx.doi.org/10.1055/s-0037-1610412.
Cheng, Hua, Cheng Chen, Rui Zhang, Jun-Chao Zhang, Wei-Yi Zhang, Yu-Qing He und Yu-Cheng Gu. „A Practical Approach for the Transamidation of N,N-Dimethyl Amides with Primary Amines Promoted by Sodium tert-Butoxide under Solvent-Free Conditions“. Synthesis 52, Nr. 21 (08.09.2020): 3286–94. http://dx.doi.org/10.1055/s-0040-1705892.
Ocampo Gutiérrez de Velasco, Diego, Aoze Su, Luhan Zhai, Satowa Kinoshita, Yuko Otani und Tomohiko Ohwada. „Unexpected Resistance to Base-Catalyzed Hydrolysis of Nitrogen Pyramidal Amides Based on the 7-Azabicyclic[2.2.1]heptane Scaffold“. Molecules 23, Nr. 9 (15.09.2018): 2363. http://dx.doi.org/10.3390/molecules23092363.
Yang, Guo-Ping, Ke Li, Wei Liu, Kai Zeng und Yu-Feng Liu. „Copper-catalyzed aerobic oxidative C–C bond cleavage of simple ketones for the synthesis of amides“. Organic & Biomolecular Chemistry 18, Nr. 35 (2020): 6958–64. http://dx.doi.org/10.1039/d0ob01601b.
Bittner, Nataly, Andy Boon, Evert H. Delbanco, Christof Walter und Angela Mally. „Assessment of aromatic amides in printed food contact materials: analysis of potential cleavage to primary aromatic amines during simulated passage through the gastrointestinal tract“. Archives of Toxicology 96, Nr. 5 (05.03.2022): 1423–35. http://dx.doi.org/10.1007/s00204-022-03254-w.
Box, Vernon G. S. „Biocidal Amidic Natural Products“. Natural Product Communications 3, Nr. 11 (November 2008): 1934578X0800301. http://dx.doi.org/10.1177/1934578x0800301111.
Xia, Ji-Bao, Yan-Lin Li und Zheng-Yang Gu. „Transition-Metal-Catalyzed Intermolecular C–H Carbonylation toward Amides“. Synlett 32, Nr. 01 (17.08.2020): 07–13. http://dx.doi.org/10.1055/s-0040-1706416.
Das, Hari S., Shyamal Das, Kartick Dey, Bhagat Singh, Rahul K. Haridasan, Arpan Das, Jasimuddin Ahmed und Swadhin K. Mandal. „Primary amides to amines or nitriles: a dual role by a single catalyst“. Chemical Communications 55, Nr. 79 (2019): 11868–71. http://dx.doi.org/10.1039/c9cc05856g.
Laclef, Sylvain, Maria Kolympadi Marković und Dean Marković. „Amide Synthesis by Transamidation of Primary Carboxamides“. Synthesis 52, Nr. 21 (04.06.2020): 3231–42. http://dx.doi.org/10.1055/s-0040-1707133.
Blondiaux, Enguerrand, und Thibault Cantat. „Efficient metal-free hydrosilylation of tertiary, secondary and primary amides to amines“. Chem. Commun. 50, Nr. 66 (2014): 9349–52. http://dx.doi.org/10.1039/c4cc02894e.
Hao, Hong-Yan, Shao-Jie Lou, Shuang Wang, Kun Zhou, Qiu-Zi Wu, Yang-Jie Mao, Zhen-Yuan Xu und Dan-Qian Xu. „Pd-catalysed β-selective C(sp3)–H arylation of simple amides“. Chemical Communications 57, Nr. 65 (2021): 8055–58. http://dx.doi.org/10.1039/d1cc02261j.
Bhalla, Tek Chand, und Harish Kumar. „Nocardia globerula NHB-2: a versatile nitrile-degrading organism“. Canadian Journal of Microbiology 51, Nr. 8 (01.08.2005): 705–8. http://dx.doi.org/10.1139/w05-046.
Radenović, Čedomir, Danica Bajuk-Bogdanović, Milica Radosavljević, Nenad Delić, Aleksandar Popović, Mile Sečanski und Miloš Crevar. „Assaying of structural parts of hybrid ZP677 grain by IC method disordered Total reflection“. Selekcija i semenarstvo 28, Nr. 1 (2022): 9–22. http://dx.doi.org/10.5937/selsem2201009r.
Weaver-Guevara, Holly M., Ryan W. Fitzgerald und Arthur Greenberg. „Rotational barriers in five related amides“. Canadian Journal of Chemistry 95, Nr. 3 (März 2017): 271–77. http://dx.doi.org/10.1139/cjc-2016-0344.
Garg, Jai Anand, Subrata Chakraborty, Yehoshoa Ben-David und David Milstein. „Unprecedented iron-catalyzed selective hydrogenation of activated amides to amines and alcohols“. Chemical Communications 52, Nr. 30 (2016): 5285–88. http://dx.doi.org/10.1039/c6cc01505k.
Bock, Hans, und Erik Heigel. „Wechselwirkungen in Molekülkristallen, 162 [1, 2]. Di(arylsulfonyl)amine – geeignete Liganden für lipophil umhüllte Polyionen-Aggregate mit Cs⊕ -Schichten variabler Dicke / Interaction in Molecular Crystals, 162 [1, 2]. Di(arylsulfonyl)amines – Ligands for Lipophilically Wrapped Polyion Aggregates with Cs⊕ -Layers of Variable Thickness“. Zeitschrift für Naturforschung B 55, Nr. 11 (01.11.2000): 1053–66. http://dx.doi.org/10.1515/znb-2000-1111.
Saha, Sayantani, und Moris S. Eisen. „Mild catalytic deoxygenation of amides promoted by thorium metallocene“. Dalton Transactions 49, Nr. 36 (2020): 12835–41. http://dx.doi.org/10.1039/d0dt02770g.
Yanev, Pavel, und Plamen Angelov. „Synthesis of functionalised β-keto amides by aminoacylation/domino fragmentation of β-enamino amides“. Beilstein Journal of Organic Chemistry 14 (10.10.2018): 2602–6. http://dx.doi.org/10.3762/bjoc.14.238.
Glover, Stephen A., Arvi Rauk, Jeanne M. Buccigross, John J. Campbell, Gerard P. Hammond, Guoning Mo, Luke E. Andrews und Ashley-Mae E. Gillson. „The HERON reaction Origin, theoretical background, and prevalence“. Canadian Journal of Chemistry 83, Nr. 9 (01.09.2005): 1492–509. http://dx.doi.org/10.1139/v05-150.
Schuhmacher, Anne, Tomoya Shiro, Sarah J. Ryan und Jeffrey W. Bode. „Synthesis of secondary and tertiary amides without coupling agents from amines and potassium acyltrifluoroborates (KATs)“. Chemical Science 11, Nr. 29 (2020): 7609–14. http://dx.doi.org/10.1039/d0sc01330g.