The O‐Directed Free Radical Hydrostannation of Propargyloxy Dialkyl Acetylenes with Ph3SnH/cat. Et3B. A Refutal of the Stannylvinyl Cation Mechanism-Reference-Cited by-同舟云学术

The O‐Directed Free Radical Hydrostannation of Propargyloxy Dialkyl Acetylenes with Ph3SnH/cat. Et3B. A Refutal of the Stannylvinyl Cation Mechanism

Published:2018-11-08 Issue:2-3 Volume:19 Page:238-319
ISSN:1527-8999
Container-title:The Chemical Record
language:en
Short-container-title:Chem. Rec.

Author:

Hale Karl J.¹,Manaviazar Soraya¹,Watson Hamish A.¹

Affiliation:

1. School of Chemistry and Chemical Engineering and the Centre for Cancer Research and Cell Biology (CCRCB)Queen's University Belfast Stranmillis Road Belfast BT9 5AG, Northern Ireland United Kingdom

Funder

Leverhulme Trust

Engineering and Physical Sciences Research Council

Publisher

Wiley

Subject

Materials Chemistry,General Chemical Engineering,Biochemistry,General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/tcr.201700104

Reference240 articles.

1. Useful new organometallic reagents for the synthesis of allylic alcohols by nucleophilic vinylation

2. Reaction of organotin hydrides with acetylenic alcohols

4. Some observations on the stereochemical and regiochemical outcome of hydrostannylation of substituted propargyl alcohols

5. Stannyldienes, new tools for organic synthesis. preparatiom and reactivity

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