Reaction of arylboronic acids and their derivatives with lead tetra-acetate. The generation of aryl–lead triacetates, and meta- and para-phenylenebis(lead triacetate), in situ for electrophilic arylation-Reference-Cited by-同舟云学术

Reaction of arylboronic acids and their derivatives with lead tetra-acetate. The generation of aryl–lead triacetates, and meta- and para-phenylenebis(lead triacetate), in situ for electrophilic arylation

Published:1990 Issue:3 Volume: Page:715-720
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Morgan Jacqueline,Pinhey John T.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1990/P1/P19900000715

Reference21 articles.

1. Use of the electrophilic arylation reaction of aryl-lead triacetates in a synthesis of (±)-lycoramine

2. Arylation with Aryllead Triacetates Produced in situ by Mercury-Lead Exchange

3. The Chemistry of Aryllead(IV) Tricarboxylates. Synthesis

4. Reaction of Aryltrialkylstannanes with Lead Tetraacetate: a Convenient Route to Aryllead Triacetates

5. R. C. Larock , ‘Organomercury Compounds in Organic Synthesis,’Springer-Verlag, Berlin, 1985, p. 15.

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