Substitution of the acetoxy groups of dialkoxymethylacetates by organometallic reagents: a route to allyl-, propargyl-, homoallyl-, homopropargyl-and α-stannylacetals

I Beaudet, A Duchêne, JL Parrain…

Index: Journal of Organometallic Chemistry, , vol. 427, # 2 p. 201 - 212

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Citation Number: 11

Abstract

... Journal of Organometallic Chemistry. ... The efficiency of the substitution of the acetoxy group is highly dependent on the nature of the organometallic reagents: soft nucleophiles with strong electrophilic assistance by the ... Tin in Organic SynthesisButterworths, London (1987). ...

An efficient synthesis of α, β??unsaturated aldehydes by a four??carbon unit extension of Grignard reagents

[Cloux, Roland; Schlosser, Manfred Helvetica Chimica Acta, 1984 , vol. 67, p. 1470 - 1474]

Substitution of the acetoxy groups of dialkoxymethylacetates by organometallic reagents: a route to allyl-, propargyl-, homoallyl-, homopropargyl-and α-stannylacetals

[Beaudet, Isabelle; Duchene, Alain; Parrain, Jean-Luc; Quintard, Jean-Paul Journal of Organometallic Chemistry, 1992 , vol. 427, # 2 p. 201 - 212]

Enantioselective synthesis of structurally intricate and complementary polyoxygenated building blocks of Spongistatin 1 (Altohyrtin A)

[Braun, Alain; Cho, Ii Hwan; Ciblat, Stephane; Clyne, Dean; Forgione, Pat; Hart, Amy C.; Huang, Guoxiang; Kim, Jungchul; Modolo, Isabelle; Paquette, Leo A.; Peng, Xiaowen; Pichlmair, Stefan; Stewart, Catherine A.; Wang, Jizhou; Zuev, Dmitry Collection of Czechoslovak Chemical Communications, 2009 , vol. 74, # 5 p. 651 - 769]

Substitution of the acetoxy groups of dialkoxymethylacetates by organometallic reagents: a route to allyl-, propargyl-, homoallyl-, homopropargyl-and α-stannylacetals

Abstract

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