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- Rhazinilam–leuconolam family of natural products: a half century of total synthesis. Fatih Sirindil, Jean-Marc Weibel, Patrick Pale, Aurélien Blanc
, Nat. Prod. Rep.
, 2022
, 39
, 1574
- Synthesis of natural products containing the pyrrolic ring. Ian S. Young, Paul D. Thornton, Alison Thompson
, Nat. Prod. Rep.
, 2010
, 27
, 1801
- A new synthetic approach to biaryls of the rhazinilam type. Application to synthesis of three novel phenylpyridine-carbamate analogues. Anne-Laure Bonneau, Nicolas Robert, Christophe Hoarau, Olivier Baudoin, Francis Marsais
, Org. Biomol. Chem.
, 2007
, 5
, 175
- Recent developments in natural product synthesis using metal-catalysed C–H bond functionalisation. Lindsay McMurray, Fionn O'Hara, Matthew J. Gaunt
, Chem. Soc. Rev.
, 2011
, 40
, 1885
- Convergent synthesis and preliminary biological evaluation of (±)-B-norrhazinal . Martin Banwell, Alison Edwards, Jason Smith, Ernest Hamel, Pascal Verdier-Pinard
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 1497
- Transition-metal catalyzed C–H activation as a means of synthesizing complex natural products. Soumya Kumar Sinha, Pintu Ghosh, Shubhanshu Jain, Siddhartha Maiti, Shaeel A. Al-Thabati, Abdulmohsen Ali Alshehri, Mohamed Mokhtar, Debabrata Maiti
, Chem. Soc. Rev.
, 2023
, 52
, 7461
- Total synthesis of (±)-rhazinal, an alkaloidal spindle toxin from Kopsia teoi. Martin G. Banwell, Alison J. Edwards, Katrina A. Jolliffe, Jason A. Smith, Ernest Hamel, Pascal Verdier-Pinard
, Org. Biomol. Chem.
, 2003
, 1
, 296
- A comprehensive review on phytochemistry and pharmacology of genus Kopsia: monoterpene alkaloids – major secondary metabolites. Nguyen Quang Hop, Ninh The Son
, RSC Adv.
, 2022
, 12
, 19171
- Methods for the synthesis of annulated pyrroles via cyclisation strategies. Wesley J. Olivier, Jason A. Smith, Alex C. Bissember
, Org. Biomol. Chem.
, 2018
, 16
, 1216
- Enantioselective palladium-catalyzed allylic alkylation reactions in the synthesis of Aspidosperma and structurally related monoterpene indole alkaloids. Beau P. Pritchett, Brian M. Stoltz
, Nat. Prod. Rep.
, 2018
, 35
, 559