Preparation of cruciferous phytoalexin related metabolites, (−)-dioxibrassinin and (−)-3-cyanomethyl-3-hydroxyoxindole, and determination of their absolute configurations by vibrational circular dichroism (VCD)
- 1 August 2003
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 44 (32) , 6017-6020
- https://doi.org/10.1016/s0040-4039(03)01513-2
Abstract
No abstract availableFunding Information
- New Energy and Industrial Technology Development Organization
- Ministry of Education, Culture, Sports, Science and Technology (14658181)
This publication has 19 references indexed in Scilit:
- Vibrational Optical Activity of Pharmaceuticals and BiomoleculesPublished by Wiley ,2000
- Synthesis and Absolute Stereochemisty of a Cruciferous Phytoalexin, (−)-SpirobrassininChemistry Letters, 2000
- Tansley Review No. 86 Accumulation of phytoalexins: defence mechanism and stimulus response systemNew Phytologist, 1996
- Marine bacteria, VIII. Maremycin A and B, new diketopiperazines from a marine Streptomyces sp.European Journal of Organic Chemistry, 1995
- Biosynthesis of Cruciferous PhytoalexinsJournal of the American Chemical Society, 1994
- Brassicanal C and two dioxindoles from cabbagePhytochemistry, 1991
- High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoidsJournal of the American Chemical Society, 1991
- Corner flapping: a simple and fast algorithm for exhaustive generation of ring conformationsJournal of the American Chemical Society, 1989
- PhytoalexinsNatural Product Reports, 1985
- 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