Complete diastereofacial selective cycloaddition of new sulfinyl dienophiles (Ss)- and (Rs)-(-)menthyl α-(2-methoxyphenylsulfoxyl)acylate with anthracene under chelation control

Article abstract of DOI:10.1080/00397919608003539

New sulfinyldienophiles (Ss)- and (Rs)- (-)menthyl α-(2-methoxyphenylsulfoxyl)acylate were prepared. Cycloadditions with anthracene in dichloromethane proceeded with complete diastereoselectivity under chelation control. Chirality at sulfur controlled dia

Full text of DOI:10.1080/00397919608003539

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Complete Diastereofacial
Selective Cycloaddition of
New Sulfinyl Dienophiles (Ss)-
and (Rs)-(-)Menthyl α-(2-
Methoxyphenylsulfoxyl)acylate
with Anthracene Under
Chelation Control
Tay-Yuan Chau a , Hsaio-Chi Lin a & Wenhao Hu b
a Department of Chemistry , National Chung-Hsing
University , Taichung, Taiwan, 40227, Republic of
China
b Union Laboratory of Asymmetric Synthesis ,
Chengdu Institute of Organic Chemistry , Chengdu,
610041
Published online: 21 Aug 2006.
To cite this article: Tay-Yuan Chau , Hsaio-Chi Lin & Wenhao Hu (1996) Complete
Diastereofacial Selective Cycloaddition of New Sulfinyl Dienophiles (Ss)-and
(Rs)-(-)Menthyl α-(2-Methoxyphenylsulfoxyl)acylate with Anthracene Under
Chelation Control, Synthetic Communications: An International Journal for
Rapid Communication of Synthetic Organic Chemistry, 26:10, 1867-1874, DOI:
10.1080/00397919608003539
To link to this article: http://dx.doi.org/10.1080/00397919608003539

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