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The biosynthesis of some sesquiterpenoids
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J. R. Hanson
Veröffentlicht/Copyright:
1. Januar 2009
Published Online: 2009-01-01
Published in Print: 1981-01-01
© 2013 Walter de Gruyter GmbH, Berlin/Boston
Artikel in diesem Heft
- New and selective reactions and reagents in natural product chemistry
- Hydrocarbons from Euphorbia lathyris
- Chiral enolate design
- Advances and perspectives of porphyrin synthesis
- A new efficient aminolysis and its application to synthesis of macrolactam alkaloids
- The biosynthesis of some sesquiterpenoids
- Total synthesis of rifamycin S
- Regio- and stereo-selective syntheses of cyclic natural products by intramolecular cycloaddition- and ene-reactions
- The leukotrienes: a new group of biologically active compounds
- Application of CMR spectroscopy to the study of porphyrin and corrin biosynthesis in vitro and in vivo
- Biologically active compounds from higher fungi
- Sesquiterpenes - biosynthetic studies with 13C and 2H magnetic resonance - a synthetic approach via homoenolization
- The role of organic synthesis in bioorganic chemistry
- Alkaloid synthesis
Artikel in diesem Heft
- New and selective reactions and reagents in natural product chemistry
- Hydrocarbons from Euphorbia lathyris
- Chiral enolate design
- Advances and perspectives of porphyrin synthesis
- A new efficient aminolysis and its application to synthesis of macrolactam alkaloids
- The biosynthesis of some sesquiterpenoids
- Total synthesis of rifamycin S
- Regio- and stereo-selective syntheses of cyclic natural products by intramolecular cycloaddition- and ene-reactions
- The leukotrienes: a new group of biologically active compounds
- Application of CMR spectroscopy to the study of porphyrin and corrin biosynthesis in vitro and in vivo
- Biologically active compounds from higher fungi
- Sesquiterpenes - biosynthetic studies with 13C and 2H magnetic resonance - a synthetic approach via homoenolization
- The role of organic synthesis in bioorganic chemistry
- Alkaloid synthesis