Author:
Verma Sonali,George Johnson,Singh Saurabh,Pardasani Pushpa,Pardasani Ramchand
Abstract
Abstract
A facile synthesis of azabicycloadducts is described by 1,3-dipolar cycloaddition reactions of thioisatin with thiazolidine-2-carboxylic acid in the presence of various electron rich and electron deficient dipolarophiles. Theoritical calculations have been performed to study the regioselectivity of products. The geometrical and energetic properties have been analyzed for the different reactants, transition states and cycloadducts formed.
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Organic Chemistry
Reference19 articles.
1. Katritzky AR, Ramsden CA: Comprehensive Heterocyclic Chemistry III. Edited by: Scriver EFV, Taylors RJK. Elsevier, New York; 2008.
2. Harwood LM, Vickers RJ: In synthetic applications of 1,3-dipolar cycloadditions chemistry toward heterocycles and natural products. Edited by: Padwa A, Pearson WH. Wiley, New York; 2003:169.
3. Gothelf KV, Kobayashi S, Jorgensen KA, eds: In cycloaddition reactions in organic synthesis. Wiley-VCH, Weinheim, Germany; 2002:211.
4. Zang H, Chan WH, Lee AWM, Xia P-F, Wong WY: Asymmetric 1,3-dipolar cycloaddition of chiral α, β-unsaturated-γ-sultams with nitrile oxides and nitrones. Lett Org Chem 2004, 1: 63–66. 10.2174/1570178043488644
5. Najera C, Sansano JM: 1,3-Dipolar cycloaddition reactions of metal stabilized azomethine ylides. Org Biomol Chem 2009, 7: 4567–4581. 10.1039/b913066g
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