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Synthesis of a simplified triazole analogue of pateamine A . A. Hemi Cumming, Sarah L. Brown, Xu Tao, Claire Cuyamendous, Jessica J. Field, John H. Miller, Joanne E. Harvey, Paul H. Teesdale-Spittle
, Org. Biomol. Chem.
, 2016
, 14
, 5117
Selective targeting of the DEAD-box RNA helicase eukaryotic initiation factor (eIF) 4A by natural products . Leo Shen, Jerry Pelletier
, Nat. Prod. Rep.
, 2020
, 37
, 609
Natural products: chemical instruments to apprehend biological symphony . Mathieu Pucheault
, Org. Biomol. Chem.
, 2008
, 6
, 424
Bridging the gap between natural product synthesis and drug discovery . Nathanyal J. Truax, Daniel Romo
, Nat. Prod. Rep.
, 2020
, 37
, 1436
Construction of sulfur-containing moieties in the total synthesis of natural products . Nengzhong Wang, Puli Saidhareddy, Xuefeng Jiang
, Nat. Prod. Rep.
, 2020
, 37
, 246
Recent advances in catalytic asymmetric aza-Cope rearrangement . Liang Wei, Chun-Jiang Wang
, Chem. Commun.
, 2021
, 57
, 10469
How different are marine microbial natural products compared to their terrestrial counterparts? . Tanja M. Voser, Max D. Campbell, Anthony R. Carroll
, Nat. Prod. Rep.
, 2022
, 39
, 7
Iron catalyzed stereoselective alkene synthesis: a sustainable pathway . Xin-Fang Duan
, Chem. Commun.
, 2020
, 56
, 14937
Structure–activity studies of the pelorusides: new congeners and semi-synthetic analogues . A. Jonathan Singh, Mina Razzak, Paul Teesdale-Spittle, Thomas N. Gaitanos, Anja Wilmes, Ian Paterson, Jonathan M. Goodman, John H. Miller, Peter T. Northcote
, Org. Biomol. Chem.
, 2011
, 9
, 4456
Amaryllidaceae, Sceletium , imidazole, oxazole, thiazole, peptide and miscellaneous alkaloids . John R. Lewis
, Nat. Prod. Rep.
, 2001
, 18
, 95