Total Synthesis of (±)?螃窿?Acoradiene via Intramolecular Photoaddition and Reductive Cyclobutane Cleavage
W Oppolzer, F Zutterman, K Bättig
Index: Oppolzer, Wolfgang; Zutterman, Freddy; Baettig, Kurt Helvetica Chimica Acta, 1983 , vol. 66, # 2 p. 522 - 533
Full Text: HTML
Citation Number: 31
Abstract
Abstract (±)-α-Acoradiene (4) has been synthesized from 3-methoxy-2-cyclohexenone by a sequence of 8 steps. The key steps (Scheme 6) are the regio-and stereoselective photo [2+ 2] addition 7 [RIGHTWARDS ARROW] 6 and the reductive fragmentation 6 [RIGHTWARDS ARROW] 5.
Related Articles:
[Hoye, Thomas R.; Martin, Steven J.; Peck, David R. Journal of Organic Chemistry, 1982 , vol. 47, # 2 p. 331 - 337]
[Yamamoto, Yoshinori; Furuta, Toshiaki Journal of Organic Chemistry, 1990 , vol. 55, # 13 p. 3971 - 3972]