Journal of the Chemical Society. Chemical communications p. 1049 - 1050 (1983)
Update date:2022-08-03
Topics: Column chromatography Yield NMR spectroscopy HPLC Chiral center Enantioselectivity Recrystallization Hydrolysis Mass spectrometry (MS) Optical rotation TLC (thin-layer chromatography) Protecting group Protection/Deprotection Reaction Monitoring β-Lactam Peptide Coupling Dipeptide Stereospecific synthesis Amino acid
Baldwin, Jack E.
Bailey, Patrick D.
Gallacher, Gerard
Singleton, Kevin A.
Wallace, Philip M.
The exotoxin, Tabtoxin, from Pseudomonas tabaci (the organism responsible for Wildfire disease of tobacco plants) has been synthesised by a stereospecific route involving, as a key stereochemistry-defining step, the cycloaddition of an acylnitroso compoun
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(1989)Doi:10.1002/ddr.20391
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(2016)Doi:10.1055/s-2006-926409
(2006)Doi:10.1016/S0040-4039(00)88420-8
(1983)
