Transformations of the tetracyclic skeleton of eudistomins by neighboring-group participation in the Mitsunobu reaction
- 1 January 1995
- journal article
- research article
- Published by Wiley in Recueil des Travaux Chimiques des Pays-Bas
- Vol. 114 (1), 27-34
- https://doi.org/10.1002/recl.19951140107
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- Antiviral and antitumor structure-activity relationship studies on tetracyclic eudistominesJournal of Medicinal Chemistry, 1992
- TheMitsunobu ReactionPublished by Wiley ,1992
- Novel Gabriel reagentsAccounts of Chemical Research, 1991
- Crystal structure determination of (1S,13bR)-1-amino-10-methoxy-1,2,7,8,13,13b-hexahydro-[1,6,2]oxathiazepino[2′,3′∶1,2]pyrido[3,4-b]indole monohydrate, C15H19N3O2S·H2OJournal of Chemical Crystallography, 1990
- Total Synthesis of (-)-Eudistomin FHETEROCYCLES, 1990
- Eudistomins From the New Zealand Ascidian Ritterella sigillinoidesAustralian Journal of Chemistry, 1989
- A revised mechanism for the Mitsunobu reactionThe Journal of Organic Chemistry, 1987
- Allyloxycarbonyl group: a versatile blocking group for nucleotide synthesisThe Journal of Organic Chemistry, 1986
- Eudistomins C, E, K, and L, potent antiviral compounds containing a novel oxathiazepine ring from the Caribbean tunicate Eudistoma olivaceumJournal of the American Chemical Society, 1984
- Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) estersJournal of the American Chemical Society, 1973