Supporting Information
Supporting Information File 1: Experimental Data | ||
Format: DOC | Size: 62.5 KB | Download |
Cite the Following Article
A short stereoselective synthesis of (+)-(6R,2′S)-cryptocaryalactone via ring-closing metathesis
Palakodety Radha Krishna, Krishnarao Lopinti and K. L. N. Reddy
Beilstein J. Org. Chem. 2009, 5, No. 14.
https://doi.org/10.3762/bjoc.5.14
How to Cite
Radha Krishna, P.; Lopinti, K.; Reddy, K. L. N. Beilstein J. Org. Chem. 2009, 5, No. 14. doi:10.3762/bjoc.5.14
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
- Kiattisewee, C.; Kaidad, A.; Jiarpinitnun, C.; Luanphaisarnnont, T. Kinetic studies of conjugate addition of amines to allenic and acrylic esters and their correlation with antibacterial activities against Staphylococcus aureus. Monatshefte für Chemie - Chemical Monthly 2018, 149, 1059–1068. doi:10.1007/s00706-018-2175-1
- Merad, J.; Borkar, P.; Caijo, F.; Pons, J.-M.; Parrain, J.-L.; Chuzel, O.; Bressy, C. Double Catalytic Kinetic Resolution (DoCKR) of Acyclic anti-1,3-Diols: The Additive Horeau Amplification. Angewandte Chemie (International ed. in English) 2017, 56, 16052–16056. doi:10.1002/anie.201709844
- Huang, F.; Xiaotong, L.; Lin, S.; Liang, C.; Huang, S.; Wang, X. Stereoselective total synthesis of (-)-(6S,2'R)-cryptocaryalactone. Natural product research 2017, 31, 2420–2427. doi:10.1080/14786419.2017.1312392
- Yet, L. Organic Reactions - Olefin Ring‐Closing Metathesis. Organic Reactions 2016, 1–1304. doi:10.1002/0471264180.or089.01
- Nagendra, S.; Reddy, V. K.; Das, B. Stereoselective Synthesis of the Non-Lactonic Portion of (Z)-Cryptofolione and Approaches towards Its Conversion to (Z)-Cryptofolione†. Helvetica Chimica Acta 2015, 98, 520–526. doi:10.1002/hlca.201400242
- Manikanta, G.; Raju, G.; Krishna, P. R. Stereoselective total synthesis of ent-hyptenolide. RSC Advances 2015, 5, 7964–7969. doi:10.1039/c4ra13708f
- Huang, F. F.; Liu, D. W.; Tang, L. J.; Wang, L.; Huang, S. P.; Wang, X. J. Synthetic Study towards the Total Synthesis of (+)-(6S,2'R)-Cryptocaryalactone. Advanced Materials Research 2014, 1033-1034, 576–578. doi:10.4028/www.scientific.net/amr.1033-1034.576
- Li, J. J. Chan alkyne reduction. Name Reactions; Springer International Publishing, 2014; pp 123–124. doi:10.1007/978-3-319-03979-4_55
- Yadav, J. S.; Bhunia, D. C.; Ganganna, B. Stereoselective total synthesis of (+)-(6R,2′S)-cryptocaryalactone and (−)-(6S,2′S)-epi cryptocaryalactone via asymmetric acetate aldol reaction. Tetrahedron Letters 2012, 53, 2496–2499. doi:10.1016/j.tetlet.2012.02.073
- Krishna, P. R.; Alivelu, M. Total Synthesis of Leiocarpin C and (+)-Goniodiol via an Olefin Cross-Metathesis Protocol. Helvetica Chimica Acta 2011, 94, 1102–1107. doi:10.1002/hlca.201000365
- Herndon, J. W. The chemistry of the carbon–transition metal double and triple bond: Annual survey covering the year 2009. Coordination Chemistry Reviews 2011, 255, 3–100. doi:10.1016/j.ccr.2010.07.003