Boron trihalide-promoted addition of aryl aldehydes to styrenes. A new convenient and highly efficient synthesis of 1,3-dihalo-1,3-diarylpropanes-Reference-Cited by-同舟云学术

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Boron trihalide-promoted addition of aryl aldehydes to styrenes. A new convenient and highly efficient synthesis of 1,3-dihalo-1,3-diarylpropanes

Published:2001-08 Issue:34 Volume:42 Page:5793-5796
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kabalka George W,Wu Zhongzhi,Ju Yuhong

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference51 articles.

1. Asymmetric ene reactions in organic synthesis

2. C2-Symmetric Copper(II) Complexes as Chiral Lewis Acids. Enantioselective Catalysis of the Glyoxylate−Ene Reaction

3. Lewis-acid catalyzed ene reactions

4. Asymmetric induction in the ene reaction of glyoxylate esters of 8-phenylmenthol

5. Acyclic stereocontrol based on chelation-controlled ene reaction with chiral α- and β-alkoxyaldehydes

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1. Halogenation of Alkenes and Dienes;Comprehensive Organic Transformations;2018-02-28

2. Boron Trichloride;Fieser and Fieser's Reagents for Organic Synthesis;2017-02-20

3. Boron Trichloride;Fieser and Fieser's Reagents for Organic Synthesis;2013-04-26

4. Boron Trihalide Mediated Haloallylation of Aryl Aldehydes and Its Application to the Preparation of (E)-1,3-Dienes;Synthesis;2011-10-20

5. Boron Trichloride;Fieser and Fieser's Reagents for Organic Synthesis;2011-08-15

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