Remote stereochemical control in asymmetric Diels–Alder reactions: synthesis of the angucycline antibiotics, (−)-tetrangomycin and MM 47755
- 1 July 2003
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 44 (28) , 5193-5196
- https://doi.org/10.1016/s0040-4039(03)01228-0
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Enantioselective Diels-Alder Approach to C-3-Oxygenated Angucyclinones from (SS)-2-(p-Tolylsulfinyl)-1,4-naphthoquinoneChemistry – A European Journal, 2000
- Short and efficient enantioselective total synthesis of angucyclinone type antibiotics (+)-rubiginone B2 and (+)-ochromycinoneChemical Communications, 1999
- Asymmetric Diels—Alder reactionsPublished by Springer Nature ,1996
- Total syntheses of the angucyclinone antibiotics (+)-emycin A and (+)-ochromycinoneChemical Communications, 1996
- Total synthesis of angucyclinones, 6. Synthesis of naturally (MM 47755; X‐14881 E) and non‐naturally occurring aromatic angucyclinonesEuropean Journal of Organic Chemistry, 1995
- Total Synthesis of Angucyclines, 4. Synthesis of rac‐TetrangomycinEuropean Journal of Organic Chemistry, 1994
- MM47755, a new benz(a)anthracene antibiotic from a streptomycete.The Journal of Antibiotics, 1989
- 6-Deoxy-8-O-methylrabelomycin and 8-O-methylrabelomycin from a Streptomyces species.The Journal of Antibiotics, 1988
- Rationally designed, chiral Lewis acid for the asymmetric induction of some Diels-Alder reactionsJournal of the American Chemical Society, 1986
- The Structural Characterization of Tetrangomycin and TetrangulolThe Journal of Organic Chemistry, 1966