Artículos de revistas sobre el tema "Isochromanes"
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Dyachenko, V. I. y V. V. Semenov. "A new approach to isochromanes". Russian Chemical Bulletin 59, n.º 4 (abril de 2010): 870–71. http://dx.doi.org/10.1007/s11172-010-0178-0.
Texto completoSaikia, Anil K., Sabera Sultana, Ngangbam Renubala Devi, Manash J. Deka, Kartikeya Tiwari y Vikash K. Dubey. "Diastereoselective synthesis of substituted hexahydrobenzo[de]isochromanes and evaluation of their antileishmanial activity". Organic & Biomolecular Chemistry 14, n.º 3 (2016): 970–79. http://dx.doi.org/10.1039/c5ob02038g.
Texto completoDyachenko, V. I. y V. V. Semenov. "ChemInform Abstract: A New Approach to Isochromanes." ChemInform 42, n.º 11 (17 de febrero de 2011): no. http://dx.doi.org/10.1002/chin.201111160.
Texto completoKuramochi, Kouji, Kazunori Tsubaki, Isoko Kuriyama, Yoshiyuki Mizushina, Hiromi Yoshida, Toshifumi Takeuchi, Shinji Kamisuki, Fumio Sugawara y Susumu Kobayashi. "Synthesis, Structure, and Cytotoxicity Studies of Some Fungal Isochromanes". Journal of Natural Products 76, n.º 9 (13 de septiembre de 2013): 1737–45. http://dx.doi.org/10.1021/np400460m.
Texto completoPihlaja, K., J. Mattinen, E. Kleinpeter, R. Meusinger, Ch Duscheck y R. Borsdorf. "A1H and13C NMR conformational study of methyl-substituted isochromanes". Magnetic Resonance in Chemistry 23, n.º 9 (septiembre de 1985): 754–58. http://dx.doi.org/10.1002/mrc.1260230915.
Texto completoLi, Xiao-Hua, Xue-Hua Han, Ling-Ling Qin, Jun-Lin He, Zhi-Xing Cao, Yu-Cheng Gu, Da-Le Guo y Yun Deng. "Isochromanes from Aspergillus fumigatus, an endophytic fungus from Cordyceps sinensis". Natural Product Research 33, n.º 13 (24 de mayo de 2018): 1870–75. http://dx.doi.org/10.1080/14786419.2018.1478824.
Texto completoYue, Guizhou, Sicheng Li, Dan Jiang, Gang Ding, Juhua Feng, Huabao Chen, Chunping Yang et al. "Syntheses of 3,3-Disubstituted Dihydrobenzofurans, Indolines, Indolinones and Isochromanes by Palladium-Catalyzed Tandem Reaction Using Pd(PPh3)2Cl2/(±)-BINAP as a Catalytic System". Catalysts 10, n.º 9 (18 de septiembre de 2020): 1084. http://dx.doi.org/10.3390/catal10091084.
Texto completoHashmi, A. Stephen K, M. Wölfle, Filiz Ata, Melissa Hamzic, Ralph Salathé y Wolfgang Frey. "Gold Catalysis: Dihydroisobenzofurans and Isochromanes by the Intramolecular Furan/Alkyne Reaction". Advanced Synthesis & Catalysis 348, n.º 16-17 (noviembre de 2006): 2501–8. http://dx.doi.org/10.1002/adsc.200600367.
Texto completoGuyard, Anne-Laure, Alain Valleix, Bernard Rousseau y Jean-Christophe Cintrat. "Synthesis and deuterium labeling of some 4-phenyl, 3-substituted isochromanes". Journal of Labelled Compounds and Radiopharmaceuticals 44, n.º 7 (2001): 529–39. http://dx.doi.org/10.1002/jlcr.484.
Texto completoSalomone, Antonio, Filippo Maria Perna, Francesca Claudia Sassone, Aurelia Falcicchio, Jure Bezenšek, Jurij Svete, Branko Stanovnik, Saverio Florio y Vito Capriati. "Preparation of Polysubstituted Isochromanes by Addition of ortho-Lithiated Aryloxiranes to Enaminones". Journal of Organic Chemistry 78, n.º 21 (24 de octubre de 2013): 11059–65. http://dx.doi.org/10.1021/jo401689e.
Texto completoTietze, Lutz F., Olaf Burkhardt y Marielouise Henrich. "Intramolecular Heck Reaction for the Synthesis of Isochromanes under Ambient and High pressure". Liebigs Annalen 1997, n.º 5 (mayo de 1997): 887–91. http://dx.doi.org/10.1002/jlac.199719970516.
Texto completoIvanov, Iliyan, Stoyanka Nikolova, Ekaterina Kochovska y Stela Statkova-Abeghe. "Application of ortho-acylated phenylacetic acid esters to the synthesis of 1-substituted isochromanes". Arkivoc 2007, n.º 15 (21 de septiembre de 2007): 31–44. http://dx.doi.org/10.3998/ark.5550190.0008.f05.
Texto completoSalomone, Antonio, Filippo Maria Perna, Francesca Claudia Sassone, Aurelia Falcicchio, Jure Bezensek, Jurij Svete, Branko Stanovnik, Saverio Florio y Vito Capriati. "ChemInform Abstract: Preparation of Polysubstituted Isochromanes by Addition of ortho-Lithiated Aryloxiranes to Enaminones." ChemInform 45, n.º 12 (6 de marzo de 2014): no. http://dx.doi.org/10.1002/chin.201412137.
Texto completoTyrrell, Elizabeth, Khatebeh Mazloumi, Donatella Banti, Paulina Sajdak, Alex Sinclair y Adam Le Gresley. "The enantiospecific synthesis of chromanes and isochromanes using a variant of an intramolecular Nicholas reaction". Tetrahedron Letters 53, n.º 33 (agosto de 2012): 4280–82. http://dx.doi.org/10.1016/j.tetlet.2012.05.112.
Texto completoAntonioletti, Roberto, Paolo Bovicelli, Benedetta Crescenzi y Paolo Lupattelli. "Improved procedure for 3,4-dihydro-1H-2-benzopyran ring closure. A general access to 3-substituted isochromanes". Tetrahedron Letters 39, n.º 37 (septiembre de 1998): 6751–52. http://dx.doi.org/10.1016/s0040-4039(98)01417-8.
Texto completoHoupis, Ioannis, Jean-Pierre Van Hoeck y Ulf Tilstam. "Carboxylate-Directed Kumada Coupling of an Acetaldehyde Synthon with 2-Bromobenzoates Used towards the Synthesis of Isochromanes". Synlett 2007, n.º 14 (13 de agosto de 2007): 2179–84. http://dx.doi.org/10.1055/s-2007-985572.
Texto completoOrue, Ane, Efraím Reyes, Jose L. Vicario, Luisa Carrillo y Uxue Uria. "Enantio- and Diastereoselective Synthesis of Substituted Tetrahydro-1H-isochromanes through a Dynamic Kinetic Resolution Proceeding under Dienamine Catalysis". Organic Letters 14, n.º 14 (5 de julio de 2012): 3740–43. http://dx.doi.org/10.1021/ol301602h.
Texto completoTrefiletti, Giuliana, Anna Rita Togna, Valentina Latina, Carolina Marra, Marcella Guiso y Giuseppina I. Togna. "1-Phenyl-6,7-dihydroxy-isochroman suppresses lipopolysaccharide-induced pro-inflammatory mediator production in human monocytes". British Journal of Nutrition 106, n.º 1 (27 de enero de 2011): 33–36. http://dx.doi.org/10.1017/s0007114510005763.
Texto completoIchikawa, Junji, Masahiro Ikeda y Masahiro Hattori. "Synthesis of Isochromanes and Isothiochromanes Bearing Fluorinated One-Carbon Units via Intramolecular Cyclizations of ortho-Substituted α-(Trifluoromethyl)styrenes". HETEROCYCLES 77, n.º 2 (2009): 1285. http://dx.doi.org/10.3987/com-08-s(f)114.
Texto completoGiles, Robin G. F., Rodney W. Rickards y Badra S. Senanayake. "Stereoselective isomerisations of 4-(3′,5′-dimethoxyphenyl)-2,5-dimethyl-1,3-dioxolanes. Temperature-dependent formation of either isochromanes or dihydroisobenzofurans". J. Chem. Soc., Perkin Trans. 1, n.º 18 (1996): 2241–48. http://dx.doi.org/10.1039/p19960002241.
Texto completode Koning, Charles B., Robin G. F. Giles, Ivan R. Green y Nazeem M. Jahed. "Mercury(II) mediated cyclisation of R-1-(1′-hydroxyethyl)-2-(1″-propenyl)-3-alkoxy-4-methoxybenzenes to chiral isochromanes". Tetrahedron 60, n.º 11 (marzo de 2004): 2629–37. http://dx.doi.org/10.1016/j.tet.2004.01.007.
Texto completoANTONIOLETTI, R., P. BOVICELLI, B. CRESCENZI y P. LUPATTELLI. "ChemInform Abstract: Improved Procedure for 3,4-Dihydro-1H-2-benzopyran Ring Closure. A General Access to 3-Substituted Isochromanes." ChemInform 29, n.º 52 (18 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199852163.
Texto completoOppong-Danquah, Ernest, Martina Blümel, Silvia Scarpato, Alfonso Mangoni y Deniz Tasdemir. "Induction of Isochromanones by Co-Cultivation of the Marine Fungus Cosmospora sp. and the Phytopathogen Magnaporthe oryzae". International Journal of Molecular Sciences 23, n.º 2 (11 de enero de 2022): 782. http://dx.doi.org/10.3390/ijms23020782.
Texto completode Koning, Charles B., Ivan R. Green, Joseph P. Michael y José R. Oliveira. "The synthesis of isochroman-4-ols and isochroman-3-ols: models for naturally occurring benzo[g]isochromanols". Tetrahedron 57, n.º 47 (noviembre de 2001): 9623–34. http://dx.doi.org/10.1016/s0040-4020(01)00963-2.
Texto completoArii, Hidekazu, Kenichi Nakao, Hideki Masuda y Takayuki Kawashima. "Synthesis of 1-Silabenzo[d,e]isochromanes via Electrophilic Aromatic Substitution of Aldehydes Activated by Silylium Ion". ACS Omega 7, n.º 6 (1 de febrero de 2022): 5166–75. http://dx.doi.org/10.1021/acsomega.1c06228.
Texto completoGILES, R. G. F., R. W. RICKARDS y B. S. SENANAYAKE. "ChemInform Abstract: Stereoselective Isomerizations of 4-(3′,5′-Dimethoxyphenyl)-2,5- dimethyl-1,3-dioxolanes. Temperature-Dependent Formation of Either Isochromanes or Dihydroisobenzofurans." ChemInform 28, n.º 11 (4 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199711043.
Texto completoGiles, Robin G. F., Rodney W. Rickards y Badra S. Senanayake. "Synthesis of isochroman-3-ylacetates and isochromane-γ-lactones through rearrangement of aryldioxolanylacetates". Journal of the Chemical Society, Perkin Transactions 1, n.º 23 (1998): 3949–56. http://dx.doi.org/10.1039/a807005i.
Texto completode Koning, Charles B., Ivan R. Green, Joseph P. Michael y Jose R. Oliveira. "ChemInform Abstract: The Synthesis of Isochroman-4-ols and Isochroman-3-ols: Models for Naturally Occurring Benzo[g]isochromanols." ChemInform 33, n.º 12 (22 de mayo de 2010): no. http://dx.doi.org/10.1002/chin.200212167.
Texto completoGiles, Robin G. F., Rodney W. Rickards y Badra S. Senanayake. "ChemInform Abstract: Synthesis of Isochroman-3-ylacetates and Isochromane-γ-lactones Through Rearrangement of Aryldioxolanylacetates." ChemInform 30, n.º 16 (16 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199916140.
Texto completoKarapetyan, Vahuni, Satenik Mkrtchyan, Jennifer Hefner, Christine Fischer y Peter Langer. "Chelation Control in the [3 + 3] Annulation Reaction of Alkoxy-Substituted 1,1-Diacylcyclopropanes with 1,3-Bis(trimethylsilyloxy)-1,3-butadienes. Diversity-Oriented Synthesis of Isochromanes". Journal of Organic Chemistry 75, n.º 3 (5 de febrero de 2010): 809–14. http://dx.doi.org/10.1021/jo902334q.
Texto completoGiles, Robin G. F., Rodney W. Rickards y Badra S. Senanayake. "Stereoselective isomerisations of 4-(2′,5′-dimethoxyphenyl)-2,5-dimethyl-1,3-dioxolanes and their 2′-chloro-5′-methoxyphenyl analogues. Temperature-dependent diastereoselective formation of isochromanes". Journal of the Chemical Society, Perkin Transactions 1, n.º 22 (1997): 3361–70. http://dx.doi.org/10.1039/a704543c.
Texto completoVerma, Ashish Kumar, Ande Chennaiah, Sateesh Dubbu y Yashwant D. Vankar. "Stereoselective synthesis of sugar-fused (or 1,2-annulated) isochromans and isochromanones by using oxa-Pictet–Spengler reaction". Organic & Biomolecular Chemistry 16, n.º 37 (2018): 8258–62. http://dx.doi.org/10.1039/c8ob01698d.
Texto completoGILES, R. G. F., R. W. RICKARDS y B. S. SENANAYAKE. "ChemInform Abstract: Stereoselective Isomerizations of 4-(2′,5′-Dimethoxyphenyl)-2,5-dimethyl-1,3-dioxolanes and Their 2′-Chloro-5′-methoxyphenyl Analogues. Temperature-Dependent Diastereoselective Formation of Isochromanes." ChemInform 29, n.º 16 (23 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199816130.
Texto completoKarapetyan, Vahuni, Satenik Mkrtchyan, Jennifer Hefner, Christine Fischer y Peter Langer. "ChemInform Abstract: Chelation Control in the [3 + 3] Annulation Reaction of Alkoxy-Substituted 1,1-Diacylcyclopropanes with 1,3-Bis(trimethylsilyloxy)-1,3-butadienes. Diversity-Oriented Synthesis of Isochromanes." ChemInform 41, n.º 22 (1 de junio de 2010): no. http://dx.doi.org/10.1002/chin.201022063.
Texto completoHamada, Shohei, Kyoko Yano, Ayano Ohshimo, Elghareeb E. Elboray, Yusuke Kobayashi y Takumi Furuta. "Oxidative C–N Bond Formation of Isochromans Using an Electronically Tuned Nitroxyl Radical as Catalyst". SynOpen 08, n.º 02 (mayo de 2024): 125–29. http://dx.doi.org/10.1055/s-0040-1720118.
Texto completoShen, B. Y., Xue-Hu Li, X. H. Lu, Z. J. Xin y A. M. Yang. "SYNTHESIS, CRYSTAL STRUCTURE ANALYSIS AND DFT STUDIES OF TWO BENZOSPIROCYCLIC KETONES". Журнал структурной химии 65, n.º 4 (2024): 125683. http://dx.doi.org/10.26902/jsc_id125683.
Texto completoLiu, Shiyao, Kazunari Nakajima y Yoshiaki Nishibayashi. "Copper-catalysed enantioselective intramolecular etherification of propargylic esters: synthetic approach to chiral isochromans". RSC Advances 9, n.º 33 (2019): 18918–22. http://dx.doi.org/10.1039/c9ra03880a.
Texto completoGiles, Robin G. F., Ivan R. Green, Yolanta Gruchlik y Francois J. Oosthuizen. "Asymmetric Syntheses of Isochroman-4,7-diols Through Intramolecular Cyclization of Tethered Lactaldehydes." Australian Journal of Chemistry 53, n.º 4 (2000): 341. http://dx.doi.org/10.1071/ch00020.
Texto completoThatikonda, Thanusha, Siddharth K. Deepake, Pawan Kumar y Utpal Das. "α-Angelica lactone catalyzed oxidation of benzylic sp3 C–H bonds of isochromans and phthalans". Organic & Biomolecular Chemistry 18, n.º 21 (2020): 4046–50. http://dx.doi.org/10.1039/d0ob00729c.
Texto completoNickerson, Leslie A., Benjamin D. Bergstrom, Mingchun Gao, Yuan-Shin Shiue, Croix J. Laconsay, Matthew R. Culberson, Walker A. Knauss, James C. Fettinger, Dean J. Tantillo y Jared T. Shaw. "Correction: Enantioselective synthesis of isochromans and tetrahydroisoquinolines by C–H insertion of donor/donor carbenes". Chemical Science 11, n.º 19 (2020): 5113. http://dx.doi.org/10.1039/d0sc90081h.
Texto completoTong, Junjie, Yang Zhang, Yang Xu, Yangyang Han, Chuan Li, Wenying Zhuang y Yongsheng Che. "Spirocitrinols A and B, citrinin derivatives with a spiro[chromane-2,3′-isochromane] skeleton from Penicillium citrinum". RSC Advances 13, n.º 9 (2023): 6124–29. http://dx.doi.org/10.1039/d3ra00665d.
Texto completoZhu, Zhengbo, Alafate Adili, Chenfei Zhao y Daniel Seidel. "Catalytic Enantioselective Approaches to the oxa-Pictet–Spengler Cyclization and Other 3,6-Dihydropyran-Forming Reactions". SynOpen 03, n.º 03 (julio de 2019): 77–90. http://dx.doi.org/10.1055/s-0039-1690686.
Texto completoCottet, Françoise, Louis Cottier y Gérard Descotes. "Photocyclisations de cétoacétals aromatiques en vue d'une approche synthétique de la crombénine". Canadian Journal of Chemistry 68, n.º 7 (1 de julio de 1990): 1251–57. http://dx.doi.org/10.1139/v90-193.
Texto completoYang, Guoping, Ke Li, Kai Zeng, Yijin Li, Tao Yu y Yufeng Liu. "Heteropolyacid ionic liquid heterogeneously catalyzed synthesis of isochromans via oxa-Pictet–Spengler cyclization in dimethyl carbonate". RSC Advances 11, n.º 18 (2021): 10610–14. http://dx.doi.org/10.1039/d1ra01004b.
Texto completoHuo, Congde, Mingxia Wu, Fengjuan Chen, Xiaodong Jia, Yong Yuan y Haisheng Xie. "Catalytic amounts of CBr4 mediated dehydrogenative coupling of isochromans with aromatic ketones". Chemical Communications 51, n.º 22 (2015): 4708–11. http://dx.doi.org/10.1039/c4cc09922b.
Texto completoWang, Hui-Hong, Xiao-Dong Wang, Fei Cao, Wei-Wei Gao, Shu-Meng Ma, Zhao Li, Xue-Mei Deng, Tao Shi y Zhen Wang. "Application of palladium-catalyzed aryl C–H alkylation in total synthesis of (−)-berkelic acid". Organic Chemistry Frontiers 8, n.º 1 (2021): 82–86. http://dx.doi.org/10.1039/d0qo01003k.
Texto completoUNTERHALT, B. y R. JOESTINGMEIER. "ChemInform Abstract: New Substituted Isochromans." ChemInform 28, n.º 1 (4 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199701169.
Texto completoOLORUNSOLA, OLUWATOBI, OLUWASEYE DADA y PENGQIAN WANG. "A SPINNING POLARIZER AND SPINNING ANALYZER METHOD FOR VISUALIZING THE ISOCHROMATES IN CONOSCOPIC INTERFEROMETERS". International Journal of Modern Physics B 27, n.º 30 (7 de noviembre de 2013): 1350175. http://dx.doi.org/10.1142/s0217979213501750.
Texto completoZhang, Ying-Qi, Xin-Qi Zhu, Yin Xu, Hao-Zhen Bu, Jia-Le Wang, Tong-Yi Zhai, Jin-Mei Zhou y Long-Wu Ye. "Synthesis of functionalized 3-isochromanones via metal-free intramolecular alkoxylation-initiated cascade cyclization". Green Chemistry 21, n.º 11 (2019): 3023–28. http://dx.doi.org/10.1039/c9gc01030k.
Texto completoVankar, Yashwant, Parasuraman Rajasekaran y Yakkala Mallikharjunarao. "Synthesis of 1C-Aryl/Alkyl 2C-Branched Sugar-Fused Isochroman Derivatives by Sequential Prins and Friedel–Crafts Cyclizations on a Perlin Aldehyde Derived Substrate". Synlett 28, n.º 11 (9 de marzo de 2017): 1346–52. http://dx.doi.org/10.1055/s-0036-1588156.
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