Exploiting the Ring Strain in Bicyclo[2.2.1]heptane Systems for the Stereoselective Preparation of Highly Functionalized Cyclopentene, Dihydrofuran, Pyrroline, and Pyrrolidine Scaffolds-Reference-Cited by-同舟云学术

Exploiting the Ring Strain in Bicyclo[2.2.1]heptane Systems for the Stereoselective Preparation of Highly Functionalized Cyclopentene, Dihydrofuran, Pyrroline, and Pyrrolidine Scaffolds

Published:2011-11-08 Issue:23 Volume:13 Page:6244-6247
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Moreno-Clavijo Elena¹,Moreno-Vargas Antonio J.¹,Kieffer Raphaëlle¹,Sigstam Thérèse¹,Carmona Ana T.¹,Robina Inmaculada¹

Affiliation:

1. Department of Organic Chemistry, Faculty of Chemistry, University of Seville, Prof. García González, 1, 41012-Seville, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol2027009

Reference28 articles.

1. Stereocontrolled Preparation of Fully Substituted Cyclopentanes: Relevance to Total Synthesis

2. Stereo-controlled synthesis of dl-prostaglandins F2.alpha. and E2

3. Total Synthesis of Prostaglandins F2α and E2 as the Naturally Occuring Forms

4. Naked sugars as synthetic intermediates. Total synthesis of L-daunosamine

5. Optically Pure 7-Oxabicyclo[2.2.1]hept-5-en-2-yl Derivatives ("Naked Sugars") as New Chirons

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