The use of solvent induced methoxy shifts as a guide to hinokiflavone structure.
- 1 January 1969
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 10 (49) , 4259-4263
- https://doi.org/10.1016/s0040-4039(01)88669-x
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- The isolation and characterization of two members of a new series of naturally occurring biflavonesCellular and Molecular Life Sciences, 1969
- New bisflavones from podocarpus and chamaecyparis plantsTetrahedron Letters, 1968
- Syntheses of Ring-substituted Flavonoids and Allied Compounds. XI. Synthesis of HinokiflavoneCHEMICAL & PHARMACEUTICAL BULLETIN, 1968
- Solvent effects in NMR SpectroscopyTetrahedron, 1968
- The Isolation of Isocryptomerin from the Leaves of Chamaecyparis obtusa ENDLICHER.YAKUGAKU ZASSHI, 1967
- On the Nuclear Magnetic Resonance Spectra of Methyl Protons of BisflavonesYAKUGAKU ZASSHI, 1967
- The Partial Demethylation of Flavones. II. Formation of IsocryptomerinCHEMICAL & PHARMACEUTICAL BULLETIN, 1967
- Chemical Constituents of the Plants of Coniferae and Allied Orders. XLVIYAKUGAKU ZASSHI, 1960
- THE STRUCTURE OF HINOKIFLAVONE, A NEW TYPE BISFLAVONOIDJournal of the American Chemical Society, 1959
- Studies on Flavonoids in the Leaves of Coniferae and Allied Plants. IVYAKUGAKU ZASSHI, 1958