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Heterocycles in organic synthesis: thiazoles and triazoles as exemplar cases of synthetic auxiliaries.

Organic & biomolecular chemistry

Dondoni A.
PMID: 20505853
Org Biomol Chem. 2010 Aug 07;8(15):3366-85. doi: 10.1039/c002586k. Epub 2010 May 26.

This Perspective article illustrates the key role of thiazole and triazole in the work carried out in the author's laboratory over three decades and deals with the synthesis of carbohydrate-based bioactive molecules. The first part reports on the development...

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Dondoni A. Heterocycles in organic synthesis: thiazoles and triazoles as exemplar cases of synthetic auxiliaries. Org Biomol Chem. 2010;8(15):3366-85doi: 10.1039/c002586k.
Dondoni, A. (2010). Heterocycles in organic synthesis: thiazoles and triazoles as exemplar cases of synthetic auxiliaries. Organic & biomolecular chemistry, 8(15), 3366-85. https://doi.org/10.1039/c002586k
Dondoni, Alessandro. "Heterocycles in organic synthesis: thiazoles and triazoles as exemplar cases of synthetic auxiliaries." Organic & biomolecular chemistry vol. 8,15 (2010): 3366-85. doi: https://doi.org/10.1039/c002586k
Dondoni A. Heterocycles in organic synthesis: thiazoles and triazoles as exemplar cases of synthetic auxiliaries. Org Biomol Chem. 2010 Aug 07;8(15):3366-85. doi: 10.1039/c002586k. Epub 2010 May 26. PMID: 20505853.
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Use of a Novel alpha-Hydroxyethylating Reagent in the Stereoselective Synthesis of Lincosamine.

The Journal of organic chemistry

van Delft FL, de Kort M, van Der Marel GA, van Boom JH.
PMID: 11667071
J Org Chem. 1996 Mar 08;61(5):1883-1885. doi: 10.1021/jo951931+.

No abstract available.

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van Delft FL, de Kort M, van Der Marel GA, et al. Use of a Novel alpha-Hydroxyethylating Reagent in the Stereoselective Synthesis of Lincosamine. J Org Chem. 1996;61(5):1883-1885doi: 10.1021/jo951931+.
van Delft, F. L., de Kort, M., van Der Marel, G. A., & van Boom, J. H. (1996). Use of a Novel alpha-Hydroxyethylating Reagent in the Stereoselective Synthesis of Lincosamine. The Journal of organic chemistry, 61(5), 1883-1885. https://doi.org/10.1021/jo951931+
van Delft, Floris L., et al. "Use of a Novel alpha-Hydroxyethylating Reagent in the Stereoselective Synthesis of Lincosamine." The Journal of organic chemistry vol. 61,5 (1996): 1883-1885. doi: https://doi.org/10.1021/jo951931+
van Delft FL, de Kort M, van Der Marel GA, van Boom JH. Use of a Novel alpha-Hydroxyethylating Reagent in the Stereoselective Synthesis of Lincosamine. J Org Chem. 1996 Mar 08;61(5):1883-1885. doi: 10.1021/jo951931+. PMID: 11667071.
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Stereoselective Synthesis of Differentially Protected Derivatives of the Higher Amino Sugars Destomic Acid and Lincosamine from Serine and Threonine.

The Journal of organic chemistry

Marshall JA, Beaudoin S.
PMID: 11666978
J Org Chem. 1996 Jan 26;61(2):581-586. doi: 10.1021/jo9517914.

The aminoheptose destomic acid (3.5) and the aminooctose lincosamine (6.8) were synthesized in protected form by parallel sequences starting from the oxazolidine derivatives 2.4 and 5.1 of N-CBz serinal and N-BOC threoninal. The parallel sequences feature BF(3)-promoted addition of...

Cite
Marshall JA, Beaudoin S. Stereoselective Synthesis of Differentially Protected Derivatives of the Higher Amino Sugars Destomic Acid and Lincosamine from Serine and Threonine. J Org Chem. 1996;61(2):581-586doi: 10.1021/jo9517914.
Marshall, J. A., & Beaudoin, S. (1996). Stereoselective Synthesis of Differentially Protected Derivatives of the Higher Amino Sugars Destomic Acid and Lincosamine from Serine and Threonine. The Journal of organic chemistry, 61(2), 581-586. https://doi.org/10.1021/jo9517914
Marshall, James A., and Beaudoin, Serge. "Stereoselective Synthesis of Differentially Protected Derivatives of the Higher Amino Sugars Destomic Acid and Lincosamine from Serine and Threonine." The Journal of organic chemistry vol. 61,2 (1996): 581-586. doi: https://doi.org/10.1021/jo9517914
Marshall JA, Beaudoin S. Stereoselective Synthesis of Differentially Protected Derivatives of the Higher Amino Sugars Destomic Acid and Lincosamine from Serine and Threonine. J Org Chem. 1996 Jan 26;61(2):581-586. doi: 10.1021/jo9517914. PMID: 11666978.
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