𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A reinvestigation of asymmetric induction in diels-alder reactions to chiral acrylates.

✍ Scribed by Wolfgang Oppolzer; Mark Kurth; Daniel Reichlin; Frank Moffatt

Publisher
Elsevier Science
Year
1981
Tongue
French
Weight
214 KB
Volume
22
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Asymmetric induction in Diels-Alder reac
Asymmetric induction in Diels-Alder reactions to acrylates derived from chiral sec-alcohols. Preliminary communication
✍ Wolfgang Oppolzer; Mark Kurth; Daniel Reichlin; Christian Chapuis; Martin Mohnha πŸ“‚ Article πŸ“… 1981 πŸ› John Wiley and Sons 🌐 German βš– 328 KB

## Abstract Starting from the enantiomerically pure monoterpenes (+)‐pulegone (**3**), (+)‐limonene (**7**), (βˆ’)‐β‐pinene (**9**), (+)‐ and (βˆ’)‐camphor (**13**) or (+)‐cholestenone (**11**) the chiral alcohols **4, 5, 6, 8, 10, 12, 14, 15, 16, 17** et **18** were prepared; their acrylates **II** un

ChemInform Abstract: Asymmetric Inductio
ChemInform Abstract: Asymmetric Induction in Thia-Dielsβ€”Alder Reactions of Chiral Polyfluoroalkylthionocarboxylates.
✍ Vadim M. Timoshenko; Sergiy A. Siry; Alexander B. Rozhenko; Yuriy G. Shermolovic πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 44 KB πŸ‘ 2 views

## 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 β€œFull Text” option. The original article is trackable v

High asymmetric induction in diels-alder
High asymmetric induction in diels-alder additions of cyclopentadiene to acrylates derived from isoborneol
✍ Wolfgang Oppolzer; Christian Chapuis; Guo Mao Dao; Daniel Reichlin; Thierry Gode πŸ“‚ Article πŸ“… 1982 πŸ› Elsevier Science 🌐 French βš– 263 KB

Starting from (R)-(+)-and from (S)-(-)-camphor the chiral alcohols 1: 2 and 3 have been prepared; their acrylates II underwent TiCl,(OR),-promoted Diels-Alder additTons to cyclopentadiene giving efficiently in a predictable manner either the (2R)-or the (2S)-adducts III with up to virtually quantita

Asymmetric induction in Diels-Alder reac
Asymmetric induction in Diels-Alder reactions of o-quinodimethanes
✍ James L. Charlton πŸ“‚ Article πŸ“… 1985 πŸ› Elsevier Science 🌐 French βš– 257 KB

Asymmetric inductive effects have been measured on the Diels-Alder reaction of dimethyl fumarate with o-quinodimethane bearing a chiral u-alkoxy group. The chiral substituents used were f-phenylethoxy, 2-(1-phenyl)propoxy, 1-(2\_phenyl)propoxy, 2-(4-phenyljbutoxy and l-cyclohexylethoxy. The greatest