## Abstract For Abstract see ChemInform Abstract in Full Text.
Approaches to the synthesis of cytochalasans. Part 5. Studies on the selectivity of the Diels-Alder reaction leading to the tetrahydroiso-indolinone sub-unit
✍ Scribed by Tibur Schmidlin; Remo Gamboni; Peter Strazewski; Christoph Tamm
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- German
- Weight
- 619 KB
- Volume
- 66
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
The stereo‐ and regiochemical course in the [2+4]cycloaddition of the chiral alkylidene malonic ester 1 to selected derivatives of (2__E__, 4__E__)‐4‐methyl‐2, 4‐hexadien‐l‐ol (2) and (2__E__, 4__E__)‐4‐methyl‐2, 4‐hexadien‐l‐al (12) has been investigated. The results are discussed on the basis of semiquantitative PMO theory.
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## Abstract For Abstract see ChemInform Abstract in Full Text.
An efficient and stereoselective approach to the synthesis of coenzyme Q 10 is described (Scheme). The MeOCH 2 -protected p-hydroquinone 4 containing the C 5 (E)-allyl (tert-butyl)dimethylsilyl ether moiety was obtained via a halogen -lithium exchange of the MeOCH 2 -proctected 2-bromo-5,6dimethoxy-