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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 3, 1973 - Issue 2
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Original Articles

Methylthiomethyl Esters (II) Transesterification and Amide Formation

Tse-Lok Ho Department of Chemistry, University of Manitoba, Winnipeg, Manitoba, Canada
&
C. M. Wong Department of Chemistry, University of Manitoba, Winnipeg, Manitoba, Canada
Pages 145-146 | Received 20 Feb 1973, Published online: 06 Dec 2006

Citations (6)

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Read on this site (3)

Tse-Lok Ho. (1979) convenient Access to Methylthiomethyl Esters. Esterification with Chlorodimethylsulfonium Salts. Synthetic Communications 9:4, pages 267-270.
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Tse-Lok Ho. (1974) α,α-Dicyanoethyl Acetate. A Reagent for Selective N-Acetylation. Synthetic Communications 4:6, pages 351-353.
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Tse-Lok Ho & Chiu Ming Wong. (1974) Deblocking of ω-Chloralkyl Esters with Sodium Sulfide. Synthetic Communications 4:5, pages 307-309.
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Articles from other publishers (3)

I Shinkai, T Liu, R.A Reamer & M Sletzinger. (1982) The synthesis of 3-(1′-hydroxyethyl)-2-azetidinone-4-yl acetic acid via dianion chemistry - an important intermediate in thienamycin total synthesis. Tetrahedron Letters 23:47, pages 4899-4902.
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Edwin Haslam. (1980) Recent developments in methods for the esterification and protection of the carboxyl group. Tetrahedron 36:17, pages 2409-2433.
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TSE‐LOK HO & C. M. WONG. (2016) ChemInform Abstract: METHYLTHIOMETHYL ESTERS(II), TRANSESTERIFICATION AND AMIDE FORMATION. Chemischer Informationsdienst 4:47.
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