An Effective and Highly Stereoselective Julia Olefination of Cyclopropyl Carbinol Mediated by CeCl3·7H2O/NaI-Reference-Cited by-同舟云学术

An Effective and Highly Stereoselective Julia Olefination of Cyclopropyl Carbinol Mediated by CeCl3·7H2O/NaI

Published:2005-06-15 Issue:14 Volume:7 Page:3069-3072
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Li Wei-Dong Z.¹,Peng Yu¹

Affiliation:

1. State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, China, and State Key Laboratory of Elemento-organic Chemistry, Nankai University, Tianjin 300071, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol051051%2B

Reference23 articles.

1. A Novel Synthesis of Functionalized Allylsilanes

2. Lanthanides in organic chemistry. 1. Selective 1,2 reductions of conjugated ketones

3. Efficient Preparation of 2-Indolyl-1-nitroalkane Derivatives Employing Nitroalkenes as Versatile Michael Acceptors: New Practical Linear Approach to Alkyl 9H-β-Carboline-4-carboxylate

4. The CeCl3·nH2O/NaI System in Organic Synthesis: An Efficient Water Tolerant Lewis Acid Promoter

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