Total synthesis of HM-1 and HM-2, aromatic sesquiterpenes isolated from the phytopathogenic fungus Helicobasidium mompa. Structure revision of HM-2
- 5 September 2005
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 46 (36) , 6105-6109
- https://doi.org/10.1016/j.tetlet.2005.06.156
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- The First Total Synthesis of the Antimicrobial Sesquiterpenes (±)-Enokipodins A and BSynlett, 2003
- Stereoselective total syntheses of (±)-1,14-herbertenediol and (±)-tochuinyl acetate and facile total syntheses of (±)-α-herbertenol, (±)-β-herbertenol and (±)-1,4-cuparenediolTetrahedron Letters, 2003
- The Development of L2X2RuCHR Olefin Metathesis Catalysts: An Organometallic Success StoryAccounts of Chemical Research, 2000
- Baker’s yeast-mediated enantioselective synthesis of the bisabolane sesquiterpenes (+)-curcuphenol, (+)-xanthorrhizol, (−)-curcuquinone and (+)-curcuhydroquinoneJournal of the Chemical Society, Perkin Transactions 1, 2000
- Herbertane-type sesquiterpenoids from the liverwort Herbertus sakuraiiPhytochemistry, 2000
- Recent advances in olefin metathesis and its application in organic synthesisTetrahedron, 1998
- Butenolides from Marchantia paleacea subspecies dipteraPhytochemistry, 1997
- Cyclopropanochroman derivatives from the liverwort Radula javanicaPhytochemistry, 1991
- Novel Phenolics from Phytopathogenic Fungus Helicobasidium mompaChemistry Letters, 1989
- Simple stereoselective version of the Claisen rearrangement leading to trans-trisubstituted olefinic bonds. Synthesis of squaleneJournal of the American Chemical Society, 1970