The synthesis of novel analogues of the manumycin family of antibiotics and the antitumour antibiotic LL-C10037α
- 18 March 1996
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 37 (12) , 2101-2104
- https://doi.org/10.1016/0040-4039(96)00203-1
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Synthesis of (-)-LL-C10037α and Related Manumycin-Type EpoxyquinolsSynthesis, 1995
- A simple and efficient procedure for the preparation of p-quinols by hypervalent iodine oxidation of phenols and phenol tripropylsilyl ethersJournal of the Chemical Society, Perkin Transactions 1, 1994
- Absolute Stereochemistry of AlisamycinBioscience, Biotechnology, and Biochemistry, 1994
- Some aspects of the stereochemistry and biosynthesis of asukamycinThe Journal of Organic Chemistry, 1993
- New compounds of the manumycin group of antibiotics and a facilitated route for their structure elucidationThe Journal of Organic Chemistry, 1993
- The Use of Pyrylium Tetrafluoroborate for the Stereoselective Synthesis of 2Z,4E-DienalsSynthesis, 1991
- A New Route to 2E,4E-Dienals from Organometallic Reagents via a Five-Carbon Homologation ProcessSynlett, 1991
- Biosynthesis of the manumycin group antibioticsJournal of the American Chemical Society, 1990
- The structure of asukamycin, a possible shunt metabolite from 3-dehydroquinic acid in the shikimate pathwayJournal of the American Chemical Society, 1979
- Sulfur-containing polypeptides. XIV. Removal of the tert-butyloxycarbonyl group with boron trifluoride etherateThe Journal of Organic Chemistry, 1971