Answers are grounded in this paper and cite their sources.
The sterereoselective total synthesis of parabactin (1) has been efficiently carried out using substituted 1,3-thiazolidine-2-thione as a leaving group.
No takes yet. Share an insight, caveat, or question.
Nagao et al. (1984) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: