Fukuyama, Tohru2009-06-042009-06-041988Tun, Min Min. "Synthetic studies towards the total synthesis of renieramycin A (Antibiotics)." (1988) Master’s Thesis, Rice University. <a href="https://hdl.handle.net/1911/13323">https://hdl.handle.net/1911/13323</a>.https://hdl.handle.net/1911/13323Formation of the skeleton of renieramycin A was achieved through sequential condensations of piperazinedione and substituted benzaldehydes. One of the key reactions of this synthesis, oxidation of benzylic position, produced hydroxylated compound 62 (see p. 22 in dissertation for illustration). Further elaboration of 62 has resulted in N-methyl 65 (p. 22), an important precursor to renieramycin A.137 p.application/pdfengCopyright is held by the author, unless otherwise indicated. Permission to reuse, publish, or reproduce the work beyond the bounds of fair use or other exemptions to copyright law must be obtained from the copyright holder.Organic chemistrySynthetic studies towards the total synthesis of renieramycin A (Antibiotics)ThesisThesis Chem. 1988 Tun