Selective alkylation of β-ketoester enolates using O-methyl aminosulfoxonium salts; the first example of C-alkylation using sulfoxonium salt electrophiles-Reference-Cited by-同舟云学术

Selective alkylation of β-ketoester enolates using O-methyl aminosulfoxonium salts; the first example of C-alkylation using sulfoxonium salt electrophiles

Published:1994 Issue:22 Volume: Page:2597-2598
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Pickersgill I. Fraser,Marchington Allan P.,Rayner Christopher M.

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1994/C3/C39940002597

Reference32 articles.

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2. D. Caine , Comprehensive Organic Synthesis, Pergamon, Oxford, 1991, vol. 3, ch. 1.1, pp. 1–65.

3. The stereoselective synthesis of .alpha.-amino acids by phase-transfer catalysis

4. Synthesis of β-hydroxy-α-amino acids by aldol condensation using a chiral phase transfer catalyst

5. Catalytic asymmetric aldol reactions. Use of a chiral (acyloxy)borane complex as a versatile Lewis-acid catalyst

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