Abstract
Novel optically active spiro-sultam-oxindole compounds with middle yields and excellent stereoselectivites were prepared through consecutive N-mesylation/cyclization reactions. The enantioselectivities of the reactants could transfer to the desired products completely.
Keywords: Oxindole, sultam, asymmetric synthesis, mesylation, cyclization.
Letters in Organic Chemistry
Title:The Asymmetric Synthesis of Spiro-Sultam-oxindoles
Volume: 11 Issue: 1
Author(s): Li-Na Fu
Affiliation:
Keywords: Oxindole, sultam, asymmetric synthesis, mesylation, cyclization.
Abstract: Novel optically active spiro-sultam-oxindole compounds with middle yields and excellent stereoselectivites were prepared through consecutive N-mesylation/cyclization reactions. The enantioselectivities of the reactants could transfer to the desired products completely.
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Cite this article as:
Fu Li-Na, The Asymmetric Synthesis of Spiro-Sultam-oxindoles, Letters in Organic Chemistry 2014; 11 (1) . https://dx.doi.org/10.2174/15701786113106660071
DOI https://dx.doi.org/10.2174/15701786113106660071 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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