IYiels-Alder reactions of 2,5,8(1If)quinoliaet were completely rcgiosekcuve for au the unsymmetrical &llert&e&uceptinthecaseofisopfaKlIliscmtspondstoa levelofregtosdectivity hi\*tban theefoundhybyviauwo&xforSSquindinecplinm. A number of studies are available on the regioselectivity of the Diels-Alde
Regioselectivity in the Diels-Alder reaction of 8,8-dimethylnaphthalene-1,4,5(8H)-trione with 2,4-hexadien-1-ol
✍ Scribed by Ramiro Araya-Maturana; Bruce K. Cassels; Tomás Delgado-Castro; Jaime A. Valderrama; Boris E. Weiss-López
- Book ID
- 108379180
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 625 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0040-4020
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## 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 “Full Text” option. The original article is trackable v
The 1,2,3,4,4a,5,8,8a-octahydro-4b,8aa -dimethylnaphthalen-4aB-ol( = dehydrogeosmin; 1) has been identitied as the olfactorily dominant compound in the flower Scents of Rebutia marsoneri WERD., Dolichothele longimummu (DC.) BR. et R., and Sulcorebutiu kruegeri (CARD.) RITT. The structure of 1, which