Expanding Stereochemical and Skeletal Diversity Using Petasis Reactions and 1,3-Dipolar Cycloadditions-Reference-Cited by-同舟云学术

Expanding Stereochemical and Skeletal Diversity Using Petasis Reactions and 1,3-Dipolar Cycloadditions

Published:2010-10-26 Issue:22 Volume:12 Page:5230-5233
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Muncipinto Giovanni¹,Kaya Taner¹,Wilson J. Anthony¹,Kumagai Naoya¹,Clemons Paul A.¹,Schreiber Stuart L.¹

Affiliation:

1. Howard Hughes Medical Institute, Broad Institute of Harvard and MIT, 7 Cambridge Center, Cambridge, Massachusetts 02142, United States, and Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol102266j

Reference50 articles.

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3. Molecular diversity by design

4. Short Synthesis of Skeletally and Stereochemically Diverse Small Molecules by Coupling Petasis Condensation Reactions to Cyclization Reactions

5. A New and Practical Synthesis of α-Amino Acids from Alkenyl Boronic Acids

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