## Abstract Key steps in the total synthesis of (+)βluciduline (IX) are asymmetric DielsβAlder reaction of 1,2βdihydropyridine with acrolein and intramolecular metathesis of the alkene (V).
Alkaloid synthesis: stereoselective approach towards fawcettimine-serratinine group of lycopodium alkaloids
β Scribed by Goverdhan Mehta; M. Sreenivasa Reddy; R. Radhakrishnan; M.V. Manjula; M.A. Viswamitra
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- French
- Weight
- 289 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
Macrocylization via formation of aryl-alkyl ether bond was a key step in a model synthesis of 14-membered cyclopeptide alkaloids. A new chemoenzymadc synthesis of chiral 2amino-l-arylethanol was developed in the course of this study
## Synthetic Studies Towards Novel Tetracyclic Lycopodium Alkaloids: A Synthesis of Deoxymagellaninone. -A novel, linear triquinanebased strategy directed towards the synthesis of tetracyclic alkaloids of the paniculatine and magellanine type is presented and applied to the preparation of deoxyma
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v