Stereochemical Diversity through Cyclodimerization: Synthesis of Polyketide-like Macrodiolides-Reference-Cited by-同舟云学术

Stereochemical Diversity through Cyclodimerization: Synthesis of Polyketide-like Macrodiolides

Published:2003-05-15 Issue:12 Volume:5 Page:2149-2152
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Su Qibin¹,Beeler Aaron B.¹,Lobkovsky Emil¹,Porco, John A.¹,Panek James S.¹

Affiliation:

1. Department of Chemistry and Center for Chemical Methodology and Library Development, Boston University, 590 Commonwealth Avenue, Boston, Massachusetts 02215, and Department of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14850

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol034608z

Reference23 articles.

1. Target-Oriented and Diversity-Oriented Organic Synthesis in Drug Discovery

2. Synthesis of natural-product-based compound libraries

3. A Strategy for Macrocyclic Ring Closure and Functionalization Aimed toward Split-Pool Syntheses

4. Stereochemistry as a Diversity Element: Solid-Phase Synthesis of Cyclic RGD Peptide Derivatives by Asymmetric Catalysis

5. Stereochemical Implications on Diversity in β-Turn Peptidomimetic Libraries

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