cheminform abstract: rationally improved chiral broensted acid for catalytic enantioselective...

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ChemInform 2009, 40, issue 44 © 2009 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim www.cheminform.wiley-vch.de Alcohols Q 0230 Rationally Improved Chiral Broensted Acid for Catalytic Enantioselective Allyl- boration of Aldehydes with an Expanded Reagent Scope. — SnCl 4 in combination with the new diol FVO is highly efficient for the asymmetric allylation, methallylation, 2-bromoallylation, and crotylation of aliphatic and aromatic aldehydes. Using this process, an access to naturally occurring (+)-dodoneine (VI) is possible. — (RAUNIYAR, V.; HALL*, D. G.; J. Org. Chem. 74 (2009) 11, 4236-4241; Dep. Chem., Univ. Alberta, Edmonton, Alberta T6G 2G2, Can.; Eng.) — Jannicke 44- 069

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Page 1: ChemInform Abstract: Rationally Improved Chiral Broensted Acid for Catalytic Enantioselective Allylboration of Aldehydes with an Expanded Reagent Scope

www.cheminform.wiley-vch.de

AlcoholsQ 0230 Rationally Improved Chiral Broensted Acid for Catalytic Enantioselective Allyl-

boration of Aldehydes with an Expanded Reagent Scope. — SnCl4 in combination with the new diol FVO is highly efficient for the asymmetric allylation, methallylation, 2-bromoallylation, and crotylation of aliphatic and aromatic aldehydes. Using this process, an access to naturally occurring (+)-dodoneine (VI) is possible. — (RAUNIYAR, V.; HALL*, D. G.; J. Org. Chem. 74 (2009) 11, 4236-4241; Dep. Chem., Univ. Alberta, Edmonton, Alberta T6G 2G2, Can.; Eng.) — Jannicke

44- 069

ChemInform 2009, 40, issue 44 © 2009 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim