trans-Acetonide Controlled endo-Selective Intramolecular Nitrone−Alkene Cycloaddition of Hept-6-enoses: A Facile Entry to Calystegines, Tropanes, and Hydroxylated Aminocycloheptanes-Reference-Cited by-同舟云学术

trans-Acetonide Controlled endo-Selective Intramolecular Nitrone−Alkene Cycloaddition of Hept-6-enoses: A Facile Entry to Calystegines, Tropanes, and Hydroxylated Aminocycloheptanes

Published:2006-12-16 Issue:2 Volume:9 Page:207-209
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Shing Tony K. M.¹,Wong Wai F.¹,Ikeno Taketo¹,Yamada Tohru¹

Affiliation:

1. Department of Chemistry and Center of Novel Functional Molecules, The Chinese University of Hong Kong, Shatin, NT, Hong Kong, China, and Department of Chemistry, Faculty of Science and Technology, Keio University, Hiyoshi, Kohoku-ku, Yokohama, 223-8522, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol062621o

Reference14 articles.

1. Tufariello, J. J. In1,3-Dipolar Cycloaddition Chemistry; Padwa, A., Ed.; Wiley: New York, 1984; Vol. 2, pp 83−168.

2. A simple route to optically active, functionalized five-, six- and seven-membered carbocyclic derivatives

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