Access to Stereodefined (E)-2-Silylallylboronates via Regioselective Chloroboration of Allenylsilanes-Reference-Cited by-同舟云学术

Access to Stereodefined (E)-2-Silylallylboronates via Regioselective Chloroboration of Allenylsilanes

Published:2019-11-12 Issue:23 Volume:21 Page:9541-9544
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Yang Zhantao¹²^ORCID,Liu Tingjie¹,Chen Xixi¹,Wan Ranran¹,Li Yang¹,Wang Xianzhen¹,Yang Chun-Hua¹^ORCID,Chang Junbiao²^ORCID

Affiliation:

1. Henan Key Laboratory of New Optoelectronic Functional Materials, College of Chemistry and Chemical Engineering, Anyang Normal University, 436 Xian’ge Road, Anyang 455000, P. R. China

2. School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, Henan 450001, P. R. China

Funder

Natural Science Foundation of Henan Province

China Postdoctoral Science Foundation

Science and Technology Department of Henan Province

National Natural Science Foundation of China

Anyang Science and Technology Bureau

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b03720

Reference30 articles.

1. Diastereoselective Allylation of Carbonyl Compounds and Imines: Application to the Synthesis of Natural Products

2. Construction of Homoallylic Alcohols from Terminal Alkynes and Aldehydes with Installation of syn-Stereochemistry

3. Copper-Catalyzed Borylcupration of Allenylsilanes

4. Synthesis of (+)-Bullatacin via the Highly Diastereoselective [3+2] Annulation Reaction of a Racemic Aldehyde and a Nonracemic Allylsilane

5. Stereoselective synthesis of terminal 1,3-butadienes by the condensation reaction of aldehydes and ketones with .gamma.-trimethylsilyl-substituted allylboranes

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