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- A review on potential of natural products in the management of COVID-19. Rudra Chakravarti, Rajveer Singh, Arijit Ghosh, Dhritiman Dey, Priyanka Sharma, Ravichandiran Velayutham, Syamal Roy, Dipanjan Ghosh
, RSC Adv.
, 2021
, 11
, 16711
- Recent developments in automated structure elucidation of natural products. Christoph Steinbeck
, Nat. Prod. Rep.
, 2004
, 21
, 512
- Recent trends in the structural revision of natural products. Bhuwan Khatri Chhetri, Serge Lavoie, Anne Marie Sweeney-Jones, Julia Kubanek
, Nat. Prod. Rep.
, 2018
, 35
, 514
- Efficient Buchwald–Hartwig and nitrene-mediated five-membered ring closure approaches to the total synthesis of quindoline. Unexpected direct conversion of a nitro group into a phosphazene. Elida N. Thobokholt, Sebastián O. Simonetti, Teodoro S. Kaufman, Enrique L. Larghi, Andrea B. J. Bracca
, RSC Adv.
, 2023
, 13
, 13715
- Recent progress in the chemistry of indole alkaloids and mould metabolites. J. E. Saxton
, Nat. Prod. Rep.
, 1994
, 11
, 493
- A concise Friedländer/Buchwald–Hartwig approach to the total synthesis of quindoline, a bioactive natural indoloquinoline alkaloid, and toward the unnatural 10-methylquindoline. María V. Méndez, Sebastian O. Simonetti, Teodoro S. Kaufman, Andrea B. J. Bracca
, New J. Chem.
, 2019
, 43
, 10803
- Efficient total synthesis of neocryptolepine and synthetic access to 6-methylquinindoline from a common intermediate. María V. Méndez, Daniel A. Heredia, Enrique L. Larghi, Andrea B. J. Bracca, Teodoro S. Kaufman
, RSC Adv.
, 2017
, 7
, 28298
- All-in-one NMR spectroscopy of small organic molecules: complete chemical shift assignment from a single NMR experiment. Veera Mohana Rao Kakita, Ramakrishna V. Hosur
, RSC Adv.
, 2020
, 10
, 21174
- Microwave-assisted reductive cyclization: an easy entry to the indoloquinolines and spiro[2H-indole-2,3′-oxindole]. Prakash T. Parvatkar, Mahesh S. Majik
, RSC Adv.
, 2014
, 4
, 22481
- Muscarine, imidazole, oxazole, thiazole and peptide alkaloids, and other miscellaneous alkaloids. John R. Lewis
, Nat. Prod. Rep.
, 1996
, 13
, 435