An easy access to functionalized diaryl ethers: Formal total synthesis of K-13
- 1 August 1994
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 35 (31) , 5649-5652
- https://doi.org/10.1016/s0040-4039(00)77270-4
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- The first examples of SNAr-based macrocyclisation: synthesis of model carboxylate-binding pockets of vancomycinJournal of the Chemical Society, Chemical Communications, 1994
- Synthesis of diaryl ethers, diaryl thioethers, and diarylamines mediated by potassium fluoride-alumina and 18-crown-6The Journal of Organic Chemistry, 1993
- Fluoride ion as a nucleophile and a leaving group in aromatic nucleophilic substitution reactionsJournal of Fluorine Chemistry, 1993
- New antitumor bicyclic hexapeptides, RA-XI, -XII, -XIII and -XIV from Rubia cordifolia.CHEMICAL & PHARMACEUTICAL BULLETIN, 1992
- The total syntheses of the isodityrosine-derived cyclic tripeptides OF4949-III and K-13. Determination of the absolute configuration of K-13Journal of the American Chemical Society, 1989
- Isolation and antitumor activity of cyclic hexapeptides isolated from Rubiae radix.CHEMICAL & PHARMACEUTICAL BULLETIN, 1984
- Studies on the antitumor cyclic hexapeptides obtained from Rubiae radix.CHEMICAL & PHARMACEUTICAL BULLETIN, 1983
- The Synthesis of Diphenyl Ethers Having Tyrosine MoietyHETEROCYCLES, 1983
- Alkali Metal Fluorides in Organic SynthesisSynthesis, 1983
- Reductive deamination of arylamines by alkyl nitrites in N,N-dimethylformamide. A direct conversion of arylamines to aromatic hydrocarbonsThe Journal of Organic Chemistry, 1977