A convenient synthesis of dialkyl 2-(2-haloethylidene)malonates, cyanoacetates and halocrotonates by one carbon extension-Reference-Cited by-同舟云学术

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A convenient synthesis of dialkyl 2-(2-haloethylidene)malonates, cyanoacetates and halocrotonates by one carbon extension

Published:2015-06 Issue:26 Volume:56 Page:4031-4035
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Sathishkumar S.,Mahasampathgowri S.,Balasubramanian K.K.,Saiganesh R.

Funder

Department of Science and Technology, Govt. of India

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference37 articles.

1. Iminium salts from .alpha.-amino acid decarbonylation. Application to the synthesis of some 1-azabicyclo[x.y.0]systems

2. Simple synthetic route to chrysanthemic acid and hemicaronic aldehyde

3. Reactivity of Electrophilic Allyl Halides

4. Verbesserte variante der knoevenagel-kondensation mit TiCl4/THF/pyridin(I). Alkyliden- und Arylidenmalonester bei 0–25°C.

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