Transannular Nitrone Cycloaddition. A Stereocontrolled Entry to the Spirocyclic Core of Pinnaic Acid
Author:
Affiliation:
1. Department of Chemistry, Oregon State University, Corvallis, Oregon 97331-4003
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol000361j
Reference17 articles.
1. Transannular Diels-Alder reaction on macrocycles. A general strategy for the synthesis of polycyclic compounds
2. Increasing the Efficiency of the Transannular Diels−Alder Strategy via Stille Macrocyclizations
3. Enantiospecific Synthesis of (+)-Byssochlamic Acid, a Nonadride from the Ascomycete Byssochlamys fulva
4. Synthesis of d-biotin from L-cystine via intramolecular [3+2]cycloaddition
5. Pinnaic acid and tauropinnaic acid: Two novel fatty acids composing a 6-azaspiro[4.5]decane unit from the Okinawan bivalve Pinna muricata
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