Artigos de revistas sobre o tema "Isochromans"
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Veja os 50 melhores artigos de revistas para estudos sobre o assunto "Isochromans".
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Hamada, Shohei, Kyoko Yano, Ayano Ohshimo, Elghareeb E. Elboray, Yusuke Kobayashi e Takumi Furuta. "Oxidative C–N Bond Formation of Isochromans Using an Electronically Tuned Nitroxyl Radical as Catalyst". SynOpen 08, n.º 02 (maio de 2024): 125–29. http://dx.doi.org/10.1055/s-0040-1720118.
Texto completo da fonteLiu, Shiyao, Kazunari Nakajima e 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 completo da fonteTrefiletti, Giuliana, Anna Rita Togna, Valentina Latina, Carolina Marra, Marcella Guiso e 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 janeiro de 2011): 33–36. http://dx.doi.org/10.1017/s0007114510005763.
Texto completo da fonteUNTERHALT, B., e 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 completo da fonteVerma, Ashish Kumar, Ande Chennaiah, Sateesh Dubbu e 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 completo da fonteThatikonda, Thanusha, Siddharth K. Deepake, Pawan Kumar e 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 completo da fonteNickerson, 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 e 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 completo da fonteUnterhalt, B., e U. Heppert. "ChemInform Abstract: Isochromans Related to Fluoxetin." ChemInform 32, n.º 38 (24 de maio de 2010): no. http://dx.doi.org/10.1002/chin.200138108.
Texto completo da fonteZhu, Zhengbo, Alafate Adili, Chenfei Zhao e Daniel Seidel. "Catalytic Enantioselective Approaches to the oxa-Pictet–Spengler Cyclization and Other 3,6-Dihydropyran-Forming Reactions". SynOpen 03, n.º 03 (julho de 2019): 77–90. http://dx.doi.org/10.1055/s-0039-1690686.
Texto completo da fonteYang, Guoping, Ke Li, Kai Zeng, Yijin Li, Tao Yu e 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 completo da fonteHuo, Congde, Mingxia Wu, Fengjuan Chen, Xiaodong Jia, Yong Yuan e 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 completo da fonteAhmar, M., e R. Bloch. "A New Synthesis of Isochromans and Phtalans". Synthetic Communications 22, n.º 10 (maio de 1992): 1417–20. http://dx.doi.org/10.1080/00397919208021607.
Texto completo da fonteMcMullin, David R., Tienabe K. Nsiama e J. David Miller. "Isochromans and α-Pyrones from Penicillium corylophilum". Journal of Natural Products 77, n.º 2 (23 de janeiro de 2014): 206–12. http://dx.doi.org/10.1021/np4005486.
Texto completo da fonteGuiso, Marcella, Carolina Marra e Claudia Cavarischia. "Isochromans from 2-(3′,4′-dihydroxy)phenylethanol". Tetrahedron Letters 42, n.º 37 (setembro de 2001): 6531–34. http://dx.doi.org/10.1016/s0040-4039(01)01307-7.
Texto completo da fonteTogna, Giuseppina I., Anna Rita Togna, Matteo Franconi, Carolina Marra e Marcella Guiso. "Olive Oil Isochromans Inhibit Human Platelet Reactivity". Journal of Nutrition 133, n.º 8 (1 de agosto de 2003): 2532–36. http://dx.doi.org/10.1093/jn/133.8.2532.
Texto completo da fonteVankar, Yashwant, Parasuraman Rajasekaran e 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 março de 2017): 1346–52. http://dx.doi.org/10.1055/s-0036-1588156.
Texto completo da fonteKhilya, V., O. Shablykina, M. Tsapko, S. Shilin, V. Moskvina, H. Bubela e Yu Zabolotna. "Eu(fod)3 EFFECT ON 1H NMR SPECTRA OF 3-ARYLISOCOUMARINS AND 3-ARYL-3,4-DIHYDROISOCOUMARINS WITH ALKOXY, ESTER AND AMIDE GROUPS". Bulletin of Taras Shevchenko National University of Kyiv. Chemistry, n.º 2(54) (2017): 74–80. http://dx.doi.org/10.17721/1728-2209.2017.2(54).15.
Texto completo da fonteYus, Miguel, Francisco Foubelo e Daniel García. "Cyclic Acetals as Precursors of Substituted Isochromans and Naphthoxepines". HETEROCYCLES 74, n.º 1 (2007): 507. http://dx.doi.org/10.3987/com-07-s(w)29.
Texto completo da fonteMao, Ying, Min Cao, Xiaoguang Pan, Jiancheng Huang, Jing Li, Liren Xu e Lei Liu. "Bimolecular oxidative C–H alkynylation of α-substituted isochromans". Organic Chemistry Frontiers 6, n.º 12 (2019): 2028–31. http://dx.doi.org/10.1039/c9qo00352e.
Texto completo da fonteZhou, Mei-Yan, Shan-Shan Kong, Ling-Qiong Zhang, Ming Zhao, Jin-Ao Duan, Zhen Ou-yang e Min Wang. "CuBr2 catalyzed bromination/oxidation of isochromans to benzaldehyde derivatives". Tetrahedron Letters 54, n.º 30 (julho de 2013): 3962–64. http://dx.doi.org/10.1016/j.tetlet.2013.05.078.
Texto completo da fonteAHMAR, M., e R. BLOCH. "ChemInform Abstract: A New Synthesis of Isochromans and Phthalans." ChemInform 23, n.º 38 (21 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199238161.
Texto completo da fonteLeibeling, Markus, Dennis C. Koester, Martin Pawliczek, Svenia C. Schild e Daniel B. Werz. "Domino access to highly substituted chromans and isochromans from carbohydrates". Nature Chemical Biology 6, n.º 3 (24 de janeiro de 2010): 199–201. http://dx.doi.org/10.1038/nchembio.302.
Texto completo da fonteDammacco, Mariangela, Leonardo Degennaro, Saverio Florio, Renzo Luisi, Biagia Musio e Angela Altomare. "Lithiation ofN-Alkyl-(o-tolyl)aziridine: Stereoselective Synthesis of Isochromans§". Journal of Organic Chemistry 74, n.º 16 (21 de agosto de 2009): 6319–22. http://dx.doi.org/10.1021/jo9011943.
Texto completo da fonteGuiso, Marcella, Carolina Marra e Rocio Rodriguez Arcos. "An investigation on dihydroxy-isochromans in extra virgin olive oil". Natural Product Research 22, n.º 16 (10 de novembro de 2008): 1403–9. http://dx.doi.org/10.1080/14786410701823942.
Texto completo da fonteZhou, Mei-Yan, Shan-Shan Kong, Ling-Qiong Zhang, Ming Zhao, Jin-Ao Duan, Ou-yang Zhen e Min Wang. "ChemInform Abstract: CuBr2Catalyzed Bromination/Oxidation of Isochromans to Benzaldehyde Derivatives." ChemInform 44, n.º 44 (14 de outubro de 2013): no. http://dx.doi.org/10.1002/chin.201344065.
Texto completo da fonteChen, Yan, e Shi-Kai Tian. "Decarboxylative Alkylation ofβ-Keto Acids with Isochromans under Oxidative Conditions". Chinese Journal of Chemistry 31, n.º 1 (27 de dezembro de 2012): 37–39. http://dx.doi.org/10.1002/cjoc.201200994.
Texto completo da fonteAlavala, Gopi Krishna Reddy, Farrukh Sajjad, Taoda Shi, Zhenghui Kang, Mingliang Ma, Dong Xing e Wenhao Hu. "Diastereoselective synthesis of isochromans via the Cu(ii)-catalysed intramolecular Michael-type trapping of oxonium ylides". Chemical Communications 54, n.º 89 (2018): 12650–53. http://dx.doi.org/10.1039/c8cc06390g.
Texto completo da fonteWei, Xiaoyi, Liangxiong Xu, Jinghua Xue, Hanhong Xu, Xingzhong Liu e Wenzhe Ma. "Three New Isochromans from the Mycelial Culture of a Cylindrocarpon Fungus". HETEROCYCLES 68, n.º 9 (2006): 1955. http://dx.doi.org/10.3987/com-06-10799.
Texto completo da fontePetrone, David A., Hasnain A. Malik, Antonin Clemenceau e Mark Lautens. "Functionalized Chromans and Isochromans via a Diastereoselective Pd(0)-Catalyzed Carboiodination". Organic Letters 14, n.º 18 (6 de setembro de 2012): 4806–9. http://dx.doi.org/10.1021/ol302111y.
Texto completo da fonteWang, Zhong, Peng Fan, Tong-Dan Xue, Lin-Lin Meng, Wen-Bin Gao, Jun Zhang, You-xing Zhao e Du-Qiang Luo. "Two New Isocoumarin Derivatives from an Endophytic Fungi Pestalotiopsis coffeae Isolated from a Mangrove Fishtail Palm". Natural Product Communications 13, n.º 1 (janeiro de 2018): 1934578X1801300. http://dx.doi.org/10.1177/1934578x1801300117.
Texto completo da fonteAmmann, Stephen E., Grant T. Rice e M. Christina White. "Terminal Olefins to Chromans, Isochromans, and Pyrans via Allylic C–H Oxidation". Journal of the American Chemical Society 136, n.º 31 (16 de julho de 2014): 10834–37. http://dx.doi.org/10.1021/ja503322e.
Texto completo da fonteHegedüs, Adrienn, e Zoltán Hell. "Zeolite-catalyzed simple synthesis of isochromans via the oxa-Pictet–Spengler reaction". Organic & Biomolecular Chemistry 4, n.º 7 (2006): 1220. http://dx.doi.org/10.1039/b601314g.
Texto completo da fonteZhou, Jimei, Chao Wang, Dong Xue, Weijun Tang, Jianliang Xiao e Chaoqun Li. "Synthesis of isochromans via Fe(OTf)2-catalyzed Oxa-Pictet–Spengler cyclization". Tetrahedron 74, n.º 49 (dezembro de 2018): 7040–46. http://dx.doi.org/10.1016/j.tet.2018.10.028.
Texto completo da fonteTemperini, Andrea, Anna Barattucci, Paola Maria Bonaccorsi, Ornelio Rosati e Lucio Minuti. "Stereoselective Synthesis of Substituted Tetrahydropyrans and Isochromans by Cyclization of Phenylseleno Alcohols". Journal of Organic Chemistry 80, n.º 16 (11 de agosto de 2015): 8102–12. http://dx.doi.org/10.1021/acs.joc.5b01199.
Texto completo da fonteLiu, Jian, Elizabeth T. Birzin, Wanda Chan, Yi Tien Yang, Lee-Yuh Pai, Carolyn DaSilva, Edward C. Hayes et al. "Estrogen receptor ligands. Part 11: Synthesis and activity of isochromans and isothiochromans". Bioorganic & Medicinal Chemistry Letters 15, n.º 3 (fevereiro de 2005): 715–18. http://dx.doi.org/10.1016/j.bmcl.2004.11.018.
Texto completo da fonteCui, Jian-Fang, Bin Yang, Qiong Yu, Nathanael Chun-Him Lai, Han Chen e Man-Kin Wong. "Silver-Mediated Organic Transformations of Propargylamines to Enones, α-Thioketones, and Isochromans". ChemistrySelect 4, n.º 4 (29 de janeiro de 2019): 1476–82. http://dx.doi.org/10.1002/slct.201900024.
Texto completo da fonteLeibeling, Markus, Bastian Milde, Daniel Kratzert, Dietmar Stalke e Daniel B. Werz. "Intermolecular Twofold Carbopalladation/Cyclization Sequence to Access Chromans and Isochromans from Carbohydrates". Chemistry - A European Journal 17, n.º 36 (2 de agosto de 2011): 9888–92. http://dx.doi.org/10.1002/chem.201101917.
Texto completo da fonteKock, Ines, Siegfried Draeger, Barbara Schulz, Brigitta Elsässer, Tibor Kurtán, Ágnes Kenéz, Sándor Antus et al. "Pseudoanguillosporin A and B: Two New Isochromans Isolated from the Endophytic FungusPseudoanguillosporasp." European Journal of Organic Chemistry 2009, n.º 9 (março de 2009): 1427–34. http://dx.doi.org/10.1002/ejoc.200801083.
Texto completo da fonteZeh, Michael, Peter Lorenz, Peter Kreutzmann e Peter Schönfeld. "Hydroxy-1-aryl-isochromans: protective compounds against lipid peroxidation and cellular nitrosative stress". Redox Report 13, n.º 1 (fevereiro de 2008): 23–30. http://dx.doi.org/10.1179/135100008x259123.
Texto completo da fonteKaufman, Teodoro S., e Enrique L. Larghi. "The Oxa-Pictet-Spengler Cyclization: Synthesis of Isochromans and Related Pyran-Type Heterocycles". Synthesis, n.º 2 (2006): 187–220. http://dx.doi.org/10.1055/s-2005-918502.
Texto completo da fonteBovicelli, Paolo, Anna Sanetti, Roberta Bernini e Paolo Lupattelli. "Oxyfunctionalisation of activated methylenes by dimethyldioxirane: An easy conversion of isochromans into isocoumarins". Tetrahedron 53, n.º 28 (julho de 1997): 9755–60. http://dx.doi.org/10.1016/s0040-4020(97)00622-4.
Texto completo da fonteXu, Yao-Chang, Elaine Lebeau, John W. Gillard e Giorgio Attardo. "Regio- and stereoselective DDQ-induced oxidative coupling of isochromans and isothiochroman with alcohols". Tetrahedron Letters 34, n.º 24 (junho de 1993): 3841–44. http://dx.doi.org/10.1016/s0040-4039(00)79242-2.
Texto completo da fonteObata, Tomoyuki, Sho Suzuki, Asuka Nakagawa, Ryota Kajihara, Keiichi Noguchi e Akio Saito. "Gold-Catalyzed Domino Synthesis of Functionalized Benzofurans and Tetracyclic Isochromans via Formal Carboalkoxylation". Organic Letters 18, n.º 16 (2 de agosto de 2016): 4136–39. http://dx.doi.org/10.1021/acs.orglett.6b02159.
Texto completo da fonteHashida, Junko, Megumi Niitsuma, Masato Iwatsuki, Mihoko Mori, Aki Ishiyama, Miyuki Namatame, Aki Nishihara-Tsukashima et al. "Panowamycins A and B, new antitrypanosomal isochromans produced by Streptomyces sp. K07-0010". Journal of Antibiotics 65, n.º 4 (25 de janeiro de 2012): 197–202. http://dx.doi.org/10.1038/ja.2011.139.
Texto completo da fonteHuo, Congde, Mingxia Wu, Fengjuan Chen, Xiaodong Jia, Yong Yuan e Haisheng Xie. "ChemInform Abstract: Catalytic Amounts of CBr4Mediated Dehydrogenative Coupling of Isochromans with Aromatic Ketones." ChemInform 46, n.º 29 (julho de 2015): no. http://dx.doi.org/10.1002/chin.201529194.
Texto completo da fonteChen, Yan, e Shi-Kai Tian. "ChemInform Abstract: Decarboxylative Alkylation of β-Keto Acids with Isochromans under Oxidative Conditions." ChemInform 44, n.º 43 (7 de outubro de 2013): no. http://dx.doi.org/10.1002/chin.201343139.
Texto completo da fontePetrone, David A., Hasnain A. Malik, Antonin Clemenceau e Mark Lautens. "ChemInform Abstract: Functionalized Chromans and Isochromans via a Diastereoselective Pd(0)-Catalyzed Carboiodination." ChemInform 44, n.º 3 (15 de janeiro de 2013): no. http://dx.doi.org/10.1002/chin.201303126.
Texto completo da fonteSyed Abuthahir, S., M. NizamMohideen, S. Mayakrishnan, N. Uma Maheswari e V. Viswanathan. "Crystal structures of two new isocoumarin derivatives: 8-amino-6-methyl-3,4-diphenyl-1H-isochromen-1-one and 8-amino-3,4-diethyl-6-methyl-1H-isochromen-1-one". Acta Crystallographica Section E Crystallographic Communications 75, n.º 8 (9 de julho de 2019): 1117–22. http://dx.doi.org/10.1107/s2056989019009435.
Texto completo da fonteBianco, A., F. Coccioli, M. Guiso e C. Marra. "The occurrence in olive oil of a new class of phenolic compounds: hydroxy-isochromans". Food Chemistry 77, n.º 4 (junho de 2002): 405–11. http://dx.doi.org/10.1016/s0308-8146(01)00366-1.
Texto completo da fonteMohler, Debra L., e David W. Thompson. "Synthesis of isochromans via the titanium tetrachloride assisted cyclization of acetals of phenethyl alcohols". Tetrahedron Letters 28, n.º 23 (janeiro de 1987): 2567–70. http://dx.doi.org/10.1016/s0040-4039(00)96149-5.
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