Supporting Information
Supporting Information File 1: Experimental details and analytical data. | ||
Format: PDF | Size: 1.2 MB | Download |
Cite the Following Article
A carbohydrate approach for the formal total synthesis of (−)-aspergillide C
Pabbaraja Srihari, Namballa Hari Krishna, Ydhyam Sridhar and Ahmed Kamal
Beilstein J. Org. Chem. 2014, 10, 3122–3126.
https://doi.org/10.3762/bjoc.10.329
How to Cite
Srihari, P.; Hari Krishna, N.; Sridhar, Y.; Kamal, A. Beilstein J. Org. Chem. 2014, 10, 3122–3126. doi:10.3762/bjoc.10.329
Download Citation
Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window
below.
Citation data in RIS format can be imported by all major citation management software, including EndNote,
ProCite, RefWorks, and Zotero.
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Starck, E.; Pascaretti, M.; Taillier, C.; Blanc, A.; Dalla, V.; Pale, P.; Weibel, J.-M. Gold(I)-Catalyzed Access to 1-Alkynyl C-Glycosides from 1-Silylated Alkynes: An Alternative Paradigm for the Direct and α-Stereoselective Alkynylation of Glycosides. ACS Catalysis 2024, 14, 14863–14870. doi:10.1021/acscatal.4c04293
- Kusaka, S.; Yamamoto, K.; Shinohara, M.; Minato, Y.; Ichikawa, S. Synthesis of capuramycin and its analogues via a Ferrier-type I reaction and their biological evaluation. Bioorganic & medicinal chemistry 2022, 73, 117011. doi:10.1016/j.bmc.2022.117011
- Pabbaraja, S.; Yasam, B. K. Total Synthesis of Marine-Derived Azole Resistant Antifungal Agent (–)-Melearoride A and Antibiotic (–)-PF1163B. SynOpen 2022, 6, 227–237. doi:10.1055/a-1942-6969
- Nasam, R.; Pabbaraja, S. A convergent total synthesis of resorcylic acid lactones zeaenol and cochliomycin A. Tetrahedron Letters 2022, 97, 153777. doi:10.1016/j.tetlet.2022.153777
- Hua, R. doi:10.1002/9783527804801.ch2
- Danilkina, N. A.; Vasileva, A.; Balova, I. A. A.E.Favorskii's scientific legacy in modern organic chemistry: Prototropic acetylene - Allene isomerization and the acetylene zipper reaction. Russian Chemical Reviews 2020, 89, 125–171. doi:10.1070/rcr4902
- Pabbaraja, S.; Gantasala, N.; Ydhyam, S.; Namballa, H. K.; Gundeboina, S.; Lambu, M. R.; Meena, S.; Datta, D. Synthesis and biological evaluation of 12-, 13-, 14-membered macrolides and open chain 2,6-trans-disubstituted dihydropyran analogues for aspergillides. Tetrahedron Letters 2018, 59, 2570–2576. doi:10.1016/j.tetlet.2018.05.056
- Liao, H.; Ma, J.; Yao, H.; Liu, X.-W. Recent progress of C-glycosylation methods in the total synthesis of natural products and pharmaceuticals. Organic & biomolecular chemistry 2018, 16, 1791–1806. doi:10.1039/c8ob00032h
- Fuwa, H.; Sasaki, M. Exploiting Ruthenium Carbene-Catalyzed Reactions in Total Synthesis of Marine Oxacyclic Natural Products. Bulletin of the Chemical Society of Japan 2016, 89, 1403–1415. doi:10.1246/bcsj.20160224
- Frihed, T. G.; Fürstner, A. Progress in the trans-Reduction and trans-Hydrometalation of Internal Alkynes. Applications to Natural Product Synthesis. Bulletin of the Chemical Society of Japan 2016, 89, 135–160. doi:10.1246/bcsj.20150317
- Seetharamsingh, B.; Khairnar, P. V.; Reddy, D. S. First Total Synthesis of Gliomasolide C and Formal Total Synthesis of Sch-725674. The Journal of organic chemistry 2015, 81, 290–296. doi:10.1021/acs.joc.5b02318
- Mahankali, B.; Srihari, P. A Carbohydrate Approach for the First Total Synthesis of Cochliomycin C: Stereoselective Total Synthesis of Paecilomycin E, Paecilomycin F and 6′‐epi‐Cochliomycin C. European Journal of Organic Chemistry 2015, 2015, 3983–3993. doi:10.1002/ejoc.201500395