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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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