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Synthesis of 6,6-bisbenzannulated spiroketals related to the rubromycins using a double intramolecular hetero-Michael addition (DIHMA)

✍ Scribed by Peter J. Choi; Dominea C.K. Rathwell; Margaret A. Brimble


Book ID
108285409
Publisher
Elsevier Science
Year
2009
Tongue
French
Weight
487 KB
Volume
50
Category
Article
ISSN
0040-4039

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πŸ“œ SIMILAR VOLUMES


ChemInform Abstract: Synthesis of 6,6-Bi
✍ Peter J. Choi; Dominea C. K. Rathwell; Margaret A. Brimble πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons βš– 30 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v

Application of the double intramolecular
✍ Junliang Hao; Craig J Forsyth πŸ“‚ Article πŸ“… 2002 πŸ› Elsevier Science 🌐 French βš– 53 KB

Application of a novel double intramolecular hetero-Michael addition (DIHMA) strategy to spiroketal synthesis was illustrated by a concise synthesis of (Β±)-(4S\*,6S\*)-4-hydroxy-1,7-dioxaspiro[5.5]undecane, a Dacus oleae olive fly pheromone.