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- Synthesis, bioactivity, and enzymatic modification of antibacterial thiotetromycin derivatives. Marlene L. Rothe, Jie Li, Ernesto Garibay, Bradley S. Moore, Shaun M. K. McKinnie
, Org. Biomol. Chem.
, 2019
, 17
, 3416
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Asymmetric synthesis of 5,5-disubstituted thiotetronic acids using an
allyl xanthate to dithiocarbonate rearrangement: total synthesis of
(5S)-thiolactomycin with revision of the absolute configuration
of the natural
. Mark S. Chambers, Eric J. Thomas
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 417
- A genomics-led approach to deciphering the mechanism of thiotetronate antibiotic biosynthesis. W. Tao, M. E. Yurkovich, S. Wen, K. E. Lebe, M. Samborskyy, Y. Liu, A. Yang, Y. Liu, Y. Ju, Z. Deng, M. Tosin, Y. Sun, P. F. Leadlay
, Chem. Sci.
, 2016
, 7
, 376
- Hot off the press. Robert A. Hill, Andrew Sutherland
, Nat. Prod. Rep.
, 2017
, 34
, 1340
- An asymmetric synthesis of thiotetronic acids using chirality transfer via an allyl xanthate-to-dithiocarbonate rearrangement. X-Ray crystal structure of (5R)-2,5-dihydro-4-hydroxy-5-methyl-3-phenyl-5-prop-1′-enyl-2-oxothiophene. Mark S. Chambers, Eric J. Thomas, David J. Williams
, J. Chem. Soc., Chem. Commun.
, 1987
, 1228
- Extremely simple and practical synthesis of (±)-vertinolide via the Michael addition. Kunihiko Takabe, Nobuyuki Mase, Masaru Nomoto, Masanori Daicho, Tetsuo Tauchi, Hidemi Yoda
, J. Chem. Soc., Perkin Trans. 1
, 2002
, 500
- 3-Ketoacyl-ACP synthase (KAS) III homologues and their roles in natural product biosynthesis. Risa Nofiani, Benjamin Philmus, Yosi Nindita, Taifo Mahmud
, Med. Chem. Commun.
, 2019
, 10
, 1517
- Total synthesis of (5S)-thiolactomycin: revision of the absolute configuration of the natural product. Mark S. Chambers, Eric J. Thomas
, J. Chem. Soc., Chem. Commun.
, 1989
, 23
- Marine natural products. Anthony R. Carroll, Brent R. Copp, Rohan A. Davis, Robert A. Keyzers, Michèle R. Prinsep
, Nat. Prod. Rep.
, 2019
, 36
, 122
- Index pages
, Nat. Prod. Rep.
, 1985
, 2
, I1