Статті в журналах з теми "Diospongin A"
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Bates, Roderick W., and Ping Song. "Synthesis of diospongin A." Tetrahedron 63, no. 21 (May 2007): 4497–99. http://dx.doi.org/10.1016/j.tet.2007.03.058.
Повний текст джерелаZúñiga, Andrea, Manuel Pérez, Zoila Gándara, Alioune Fall, Generosa Gómez, and Yagamare Fall. "Synthesis of diospongin A, ent-diospongin A and C-5 epimer of diospongin B from tri-O-acetyl-D-glucal." Arkivoc 2015, no. 7 (October 22, 2015): 195–215. http://dx.doi.org/10.3998/ark.5550190.p009.191.
Повний текст джерелаBharath, Yada, Utkal Mani Choudhury, N. Sadhana, and Debendra K. Mohapatra. "The Mukaiyama type aldol reaction for the synthesis of trans-2,6-disubstituted tetrahydropyrans: synthesis of diospongin A and B." Organic & Biomolecular Chemistry 17, no. 41 (2019): 9169–81. http://dx.doi.org/10.1039/c9ob01549c.
Повний текст джерелаVaithegi, Kannan, and Kavirayani R. Prasad. "Total synthesis of (+)-diospongin A." Tetrahedron 76, no. 47 (November 2020): 131625. http://dx.doi.org/10.1016/j.tet.2020.131625.
Повний текст джерелаChandrasekhar, S., T. Shyamsunder, S. Jaya Prakash, A. Prabhakar, and B. Jagadeesh. "First total synthesis of (−)-diospongin B." Tetrahedron Letters 47, no. 1 (January 2006): 47–49. http://dx.doi.org/10.1016/j.tetlet.2005.10.129.
Повний текст джерелаMeruva, Suresh Babu, Ramamohan Mekala, Akula Raghunadh, K. Raghavendra Rao, Vilas H. Dahanukar, T. V. Pratap, U. K. Syam Kumar, and P. K. Dubey. "Synthesis of tetrahedral diarylheptanoid ent-diospongin A and epimer-diospongin B by employing Julia–Kocienski olefination." Tetrahedron Letters 55, no. 34 (August 2014): 4739–41. http://dx.doi.org/10.1016/j.tetlet.2014.06.112.
Повний текст джерелаCossy, Janine, Cyril Bressy, and Florent Allais. "A Short and Efficient Synthesis of (-)-Diospongin A." Synlett 2006, no. 20 (December 2006): 3455–56. http://dx.doi.org/10.1055/s-2006-956485.
Повний текст джерелаHiebel, Marie-Aude, Béatrice Pelotier, and Olivier Piva. "Total synthesis of (+/−)-diospongin A via Prins reaction." Tetrahedron 63, no. 33 (August 2007): 7874–78. http://dx.doi.org/10.1016/j.tet.2007.05.089.
Повний текст джерелаHo, Tse-Lok, Bin Tang, Guohua Ma, and Pengfei Xu. "Concise Synthesis of Yashabushidiol A and (±)-Diospongin A." Journal of the Chinese Chemical Society 59, no. 3 (March 2012): 455–58. http://dx.doi.org/10.1002/jccs.201100664.
Повний текст джерелаMeruva, Suresh Babu, Ramamohan Mekala, Akula Raghunadh, K. Raghavendra Rao, Vilas H. Dahanukar, T. V. Pratap, U. K. Syam Kumar, and P. K. Dubey. "ChemInform Abstract: Synthesis of Tetrahedral Diarylheptanoid ent-Diospongin A (I) and epimer-Diospongin B (II) by Employing Julia-Kocienski Olefination." ChemInform 46, no. 5 (January 15, 2015): no. http://dx.doi.org/10.1002/chin.201505215.
Повний текст джерелаReddy, Chada Raji, Guvvala Balakrishna Reddy, and Boinapally Srikanth. "Stereoselective synthesis of a tetrahydropyranyl diarylheptanoid, ent-diospongin A." Tetrahedron: Asymmetry 22, no. 18-19 (October 2011): 1725–28. http://dx.doi.org/10.1016/j.tetasy.2011.10.006.
Повний текст джерелаChandrasekhar, S., G. S. Kiran Babu, and Ch Raji Reddy. "Asymmetric synthesis of aza-diospongin A as an iNOS inducer." Tetrahedron: Asymmetry 20, no. 19 (October 2009): 2216–19. http://dx.doi.org/10.1016/j.tetasy.2009.09.013.
Повний текст джерелаKumar, Rayala Naveen, and H. M. Meshram. "Total synthesis of (−)-diospongin A and (+)-cryptofolione via asymmetric aldol reaction." Tetrahedron Letters 52, no. 9 (March 2011): 1003–7. http://dx.doi.org/10.1016/j.tetlet.2010.12.070.
Повний текст джерелаMore, Jesse. "Synthesis of (±)-Diospongin A: A Hetero-Diels-Alder and C-Glycosylation Approach." Synthesis 2010, no. 14 (May 10, 2010): 2419–23. http://dx.doi.org/10.1055/s-0029-1218784.
Повний текст джерелаMore, Jesse D. "ChemInform Abstract: Synthesis of (.+-.)-Diospongin A: A Hetero-Diels-Alder and C-Glycosylation Approach." ChemInform 41, no. 48 (November 4, 2010): no. http://dx.doi.org/10.1002/chin.201048209.
Повний текст джерелаYadav, J., B. Padmavani, B. V. Reddy, Ch Venugopal, and A. Rao. "Total Synthesis of Diospongin A via an Enzymatic Kinetic Resolution of (±)-Tetrahydropyranol Derived from Prins Cyclization." Synlett 2007, no. 13 (July 12, 2007): 2045–48. http://dx.doi.org/10.1055/s-2007-984886.
Повний текст джерелаKarlubíková, Ol'ga, Matej Babjak, and Tibor Gracza. "Tetrahydropyran synthesis by palladium(II)-catalysed hydroxycarbonylation of hexenols: synthesis of (±)-diospongin A and (+)-civet cat compound." Tetrahedron 67, no. 27-28 (July 2011): 4980–87. http://dx.doi.org/10.1016/j.tet.2011.04.045.
Повний текст джерелаGharpure, Santosh J., Sumit P. Mane, Laxmi Narayan Nanda, and Manoj Kumar Shukla. "Stereoselective Synthesis of Donor-Acceptor Cyclopropapyranone by Intramolecular Cyclopropanation of Vinylogous Carbonates: Application to the Total Synthesis of (±)-Diospongin B." Israel Journal of Chemistry 56, no. 6-7 (January 6, 2016): 553–57. http://dx.doi.org/10.1002/ijch.201500088.
Повний текст джерелаTong, Rongbiao, and Zhilong Li. "Asymmetric Total Syntheses of the trans-2-Aryl-6-alkyltetrahydropyrans Diospongin B and Parvistones D and E from a Common Precursor." Synthesis 48, no. 11 (April 12, 2016): 1630–36. http://dx.doi.org/10.1055/s-0035-1561592.
Повний текст джерелаRybak, Taras, and Dennis G. Hall. "Stereoselective and Regiodivergent Allylic Suzuki–Miyaura Cross-Coupling of 2-Ethoxydihydropyranyl Boronates: Synthesis and Confirmation of Absolute Stereochemistry of Diospongin B." Organic Letters 17, no. 17 (August 20, 2015): 4156–59. http://dx.doi.org/10.1021/acs.orglett.5b01906.
Повний текст джерелаTadiparthi, Krishnaji, and Sourav Chatterjee. "Synthetic Approaches to Diospongins: A Two Decade Journey." SynOpen 06, no. 03 (July 2022): 141–57. http://dx.doi.org/10.1055/s-0040-1720032.
Повний текст джерелаRybak, Taras, and Dennis G. Hall. "ChemInform Abstract: Stereoselective and Regiodivergent Allylic Suzuki-Miyaura Cross-Coupling of 2-Ethoxydihydropyranyl Boronates: Synthesis and Confirmation of Absolute Stereochemistry of Diospongin B." ChemInform 47, no. 4 (January 2016): no. http://dx.doi.org/10.1002/chin.201604130.
Повний текст джерелаClarke, Paul A., Nadiah Mad Nasir, Philip B. Sellars, Alejandra M. Peter, Connor A. Lawson, and James L. Burroughs. "Synthesis of 2,6-trans- and 3,3,6-trisubstituted tetrahydropyran-4-ones from Maitland–Japp derived 2H-dihydropyran-4-ones: a total synthesis of diospongin B." Organic & Biomolecular Chemistry 14, no. 28 (2016): 6840–52. http://dx.doi.org/10.1039/c6ob01182a.
Повний текст джерелаLee, Kiyoun, Hyoungsu Kim, and Jiyong Hong. "A Facile and Efficient Synthesis of 4-Hydroxy-2,6-cis-tetrahydropyrans via Tandem Cross-Metathesis/Thermal SN2′ Reaction: Protecting-Group-Free Synthesis of (±)-Diospongin A." Organic Letters 11, no. 22 (November 19, 2009): 5202–5. http://dx.doi.org/10.1021/ol902125d.
Повний текст джерелаYao, Hongliang, Jingyun Ren, and Rongbiao Tong. "A short and flexible route to tetrahydropyran-4-ones via conjugated nitrile oxidescycloaddition and oxa-Michael cyclization: a concise diastereoselective total synthesis of (±)-diospongin A." Chem. Commun. 49, no. 2 (2013): 193–95. http://dx.doi.org/10.1039/c2cc37772a.
Повний текст джерелаKumaraswamy, Gullapalli, and Dasa Rambabu. "A flexible enantioselective synthesis of (+)-centrolobine and 5-epi-diospongin-A using asymmetric transfer hydrogenation/tandem Grubbs cross-metathesis/oxy-Michael reaction as key steps." Tetrahedron: Asymmetry 24, no. 4 (February 2013): 196–201. http://dx.doi.org/10.1016/j.tetasy.2013.01.005.
Повний текст джерелаYao, Hongliang, Jingyun Ren, and Rongbiao Tong. "ChemInform Abstract: A Short and Flexible Route to Tetrahydropyran-4-ones via Conjugated Nitrile Oxides Cycloaddition and Oxa-Michael Cyclization: A Concise Diastereoselective Total Synthesis of (.+-.)-Diospongin A." ChemInform 44, no. 20 (April 25, 2013): no. http://dx.doi.org/10.1002/chin.201320153.
Повний текст джерелаXian, Ming, Hua Wang, and Brian Shuhler. "Total Syntheses of Diospongins A and B." Synlett 2008, no. 17 (October 1, 2008): 2651–54. http://dx.doi.org/10.1055/s-0028-1083518.
Повний текст джерелаStefan, Eric, Ansel P. Nalin, and Richard E. Taylor. "Concise enantioselective synthesis of diospongins A and B." Tetrahedron 69, no. 36 (September 2013): 7706–12. http://dx.doi.org/10.1016/j.tet.2013.05.081.
Повний текст джерелаSabitha, Gowravaram, Pannala Padmaja, and Jhillu S Yadav. "A Concise Total Synthesis of Diospongins A and B." Helvetica Chimica Acta 91, no. 12 (December 2008): 2235–39. http://dx.doi.org/10.1002/hlca.200890242.
Повний текст джерелаKawai, Nobuyuki, Sudhir Mahadeo Hande, and Jun'ichi Uenishi. "Stereoselective synthesis of (−)-diospongins A and B and their stereoisomers at C-5." Tetrahedron 63, no. 37 (September 2007): 9049–56. http://dx.doi.org/10.1016/j.tet.2007.06.081.
Повний текст джерелаSawant, Kailas B., та Michael P. Jennings. "Efficient Total Syntheses and Structural Verification of Both Diospongins A and B via a Common δ-Lactone Intermediate". Journal of Organic Chemistry 71, № 20 (вересень 2006): 7911–14. http://dx.doi.org/10.1021/jo061296f.
Повний текст джерелаPiva, Olivier, Ludovic Raffier, and Frédéric Izquierdo. "Desymmetrization of Hepta-1,6-dien-4-ol by Prins Reaction and Subsequent Cross-Metathesis: Access to Diospongine A Homologues." Synthesis 2011, no. 24 (November 4, 2011): 4037–44. http://dx.doi.org/10.1055/s-0031-1289588.
Повний текст джерелаAnada, Masahiro, Takuya Washio, Yudai Watanabe, Koji Takeda, and Shunichi Hashimoto. "A Short, Catalytic, Asymmetric Synthesis of Diospongins A and B by a One-Pot, Sequential Hetero-Diels-Alder/Mukaiyama-Michael Reaction Process." European Journal of Organic Chemistry 2010, no. 35 (October 27, 2010): 6850–54. http://dx.doi.org/10.1002/ejoc.201001125.
Повний текст джерелаKumaraswamy, Gullapalli, Gajula Ramakrishna, Police Naresh, Bharatam Jagadeesh, and Balasubramanian Sridhar. "A Flexible Enantioselective Total Synthesis of Diospongins A and B and Their Enantiomers Using Catalytic Hetero-Diels−Alder/Rh-Catalyzed 1,4-Addition and Asymmetric Transfer Hydrogenation Reactions as Key Steps." Journal of Organic Chemistry 74, no. 21 (November 6, 2009): 8468–71. http://dx.doi.org/10.1021/jo901739y.
Повний текст джерелаBates, Roderick W., and Ping Song. "Synthesis of Diospongin A." ChemInform 38, no. 35 (August 28, 2007). http://dx.doi.org/10.1002/chin.200735215.
Повний текст джерелаChandrasekhar, S., T. Shyamsunder, S. Jaya Prakash, A. Prabhakar, and B. Jagadeesh. "First Total Synthesis of (-)-Diospongin B." ChemInform 37, no. 18 (May 2, 2006). http://dx.doi.org/10.1002/chin.200618220.
Повний текст джерелаHiebel, Marie-Aude, Beatrice Pelotier, and Olivier Piva. "Total Synthesis of (+/-)-Diospongin A via Prins Reaction." ChemInform 38, no. 47 (November 20, 2007). http://dx.doi.org/10.1002/chin.200747205.
Повний текст джерелаBressy, Cyril, Florent Allais, and Janine Cossy. "A Short and Efficient Synthesis of (-)-Diospongin A." ChemInform 38, no. 17 (April 24, 2007). http://dx.doi.org/10.1002/chin.200717197.
Повний текст джерелаJun, Yin, Liu Zhihui, Han Na, and Xiao Bin. "Relative and Absolute Structures of Diospongin A, B and C." Planta Medica 75, no. 04 (March 2009). http://dx.doi.org/10.1055/s-2009-1216410.
Повний текст джерелаChandrasekhar, S., G. S. Kiran Babu, and Ch Raji Reddy. "ChemInform Abstract: Asymmetric Synthesis of aza-Diospongin as an iNOS Inducer." ChemInform 41, no. 12 (March 23, 2010). http://dx.doi.org/10.1002/chin.201012194.
Повний текст джерелаYadav, J. S., B. Padmavani, B. V. Subba Reddy, Ch Venugopal, and A. Bhaskar Rao. "ChemInform Abstract: Total Synthesis of Diospongin A via an Enzymatic Kinetic Resolution of (.+-.)-Tetrahydropyranol Derived from Prins Cyclization." ChemInform 39, no. 1 (January 1, 2008). http://dx.doi.org/10.1002/chin.200801218.
Повний текст джерелаGharpure, Santosh J., Sumit P. Mane, Laxmi Narayan Nanda, and Manoj Kumar Shukla. "ChemInform Abstract: Stereoselective Synthesis of Donor-Acceptor Cyclopropapyranone by Intramolecular Cyclopropanation of Vinylogous Carbonates: Application to the Total Synthesis of (.+-.)-Diospongin B." ChemInform 47, no. 47 (November 2016). http://dx.doi.org/10.1002/chin.201647152.
Повний текст джерелаLi, Zhilong, and Rongbiao Tong. "ChemInform Abstract: Asymmetric Total Syntheses of the trans-2-Aryl-6-alkyltetrahydropyrans Diospongin B and Parvistones D and E from a Common Precursor." ChemInform 47, no. 43 (October 2016). http://dx.doi.org/10.1002/chin.201643180.
Повний текст джерелаClarke, Paul A., Nadiah Mad Nasir, Philip B. Sellars, Alejandra M. Peter, Connor A. Lawson, and James L. Burroughs. "ChemInform Abstract: Synthesis of 2,6-trans- and 3,3,6-Trisubstituted Tetrahydropyran-4-ones from Maitland-Japp Derived 2H-Dihydropyran-4-ones: A Total Synthesis of Diospongin B." ChemInform 47, no. 49 (November 2016). http://dx.doi.org/10.1002/chin.201649147.
Повний текст джерелаSabitha, Gowravaram, Pannala Padmaja, and Jhillu S. Yadav. "ChemInform Abstract: A Concise Total Synthesis of Diospongins A (VII) and B (VIII)." ChemInform 40, no. 18 (May 5, 2009). http://dx.doi.org/10.1002/chin.200918195.
Повний текст джерелаKawai, Nobuyuki, Sudhir Mahadeo Hande, and Jun'ichi Uenishi. "ChemInform Abstract: Stereoselective Synthesis of (-)-Diospongins A and B and Their Stereoisomers at C-5." ChemInform 39, no. 4 (January 22, 2008). http://dx.doi.org/10.1002/chin.200804221.
Повний текст джерелаSawant, Kailas B., та Michael P. Jennings. "Efficient Total Syntheses and Structural Verification of Both Diospongins A (IIa) and B (IIb) via a Common δ-Lactone Intermediate (I)." ChemInform 38, № 6 (6 лютого 2007). http://dx.doi.org/10.1002/chin.200706195.
Повний текст джерелаKumaraswamy, Gullapalli, Gajula Ramakrishna, Police Naresh, Bharatam Jagadeesh, and Balasubramanian Sridhar. "ChemInform Abstract: A Flexible Enantioselective Total Synthesis of Diospongins A (I) and B (II) and Their Enantiomers Using Catalytic Hetero-Diels-Alder/Rh-Catalyzed 1,4-Addition and Asymmetric Transfer Hydrogenation Reactions as Key Steps." ChemInform 41, no. 12 (March 23, 2010). http://dx.doi.org/10.1002/chin.201012196.
Повний текст джерела