Weaker Lewis acid, better catalytic activity: dual mechanisms in perfluoroarylborane-catalyzed allylstannation reactions

Morrison, DJ; Piers, WE

HERO ID

3860797

Reference Type

Journal Article

Year

2003

Language

English

PMID

12889892

HERO ID 3860797
In Press No
Year 2003
Title Weaker Lewis acid, better catalytic activity: dual mechanisms in perfluoroarylborane-catalyzed allylstannation reactions
Authors Morrison, DJ; Piers, WE
Journal Organic Letters
Volume 5
Issue 16
Page Numbers 2857-2860
Abstract [reaction: see text] PhB(C(6)F(5))(2) exhibits much higher activity as a Lewis acid catalyst for the allylstannation of aromatic aldehydes than the stronger Lewis acid B(C(6)F(5))(3). This anomalous enhancement of catalytic activity for the weaker LA is shown to be partly due to decreased thermodynamic stability of ion pair 2b relative to 2a in the product-forming step of the reaction. A mechanistic path where the borane serves as the true LA catalyst is more important for the weakly Lewis acidic borane.
Doi 10.1021/ol034928i
Pmid 12889892
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English