Abstract
Since the period of the 1940s, 2-aminopropane-1,3-diol (“serinol”) and its commercial C-substituted analogous are a popular motif in organic compounds covering almost all facets of organic synthesis. This first part of the review deals mainly with the nowadays approaches focused on serinolsreactivity with carbonyl electrophiles (aldehydes and ketones) as well as its applications.
Keywords: 2-aminopropane-1,3-diols, ring-chain tautomerism, 1,3-oxazolidines, 3,7-dioxa-1-azabicyclo[3.3.0]octanes, 5-amino-1,3-dioxanes, asymmetric synthesis
Current Organic Synthesis
Title: (Masked)serinols: Molecules, Biomolecules, Building-Blocks, Supramolecules.Part (I): Syntheses Based on Serinols Reactivity with Carbonyl Electrophiles
Volume: 7 Issue: 2
Author(s): Mircea Darabantu
Affiliation:
Keywords: 2-aminopropane-1,3-diols, ring-chain tautomerism, 1,3-oxazolidines, 3,7-dioxa-1-azabicyclo[3.3.0]octanes, 5-amino-1,3-dioxanes, asymmetric synthesis
Abstract: Since the period of the 1940s, 2-aminopropane-1,3-diol (“serinol”) and its commercial C-substituted analogous are a popular motif in organic compounds covering almost all facets of organic synthesis. This first part of the review deals mainly with the nowadays approaches focused on serinolsreactivity with carbonyl electrophiles (aldehydes and ketones) as well as its applications.
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Cite this article as:
Darabantu Mircea, (Masked)serinols: Molecules, Biomolecules, Building-Blocks, Supramolecules.Part (I): Syntheses Based on Serinols Reactivity with Carbonyl Electrophiles, Current Organic Synthesis 2010; 7 (2) . https://dx.doi.org/10.2174/157017910790820300
DOI https://dx.doi.org/10.2174/157017910790820300 |
Print ISSN 1570-1794 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6271 |

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