𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Stereoselective total synthesis of dinemasone A by double intramolecular hetero-Michael addition (DIHMA)

✍ Scribed by Sharma, Gangavaram V. M.; Srikanth, Gourishetty; Reddy, Pothula Purushotham

Book ID
118152887
Publisher
Royal Society of Chemistry
Year
2012
Tongue
English
Weight
348 KB
Volume
10
Category
Article
ISSN
1477-0520

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: Synthesis of 6,6-Bi
ChemInform Abstract: Synthesis of 6,6-Bisbenzannulated Spiroketals Related to the Rubromycins Using a Double Intramolecular Hetero-Michael Addition (DIHMA).
✍ 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
Application of the double intramolecular hetero-Michael addition (DIHMA) approach in spiroketal synthesis: total synthesis of (Β±)-(4S*,6S*)-4-hydroxy-1,7-dioxaspiro[5.5]undecane, a Dacus oleae olive fly pheromone
✍ 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.