1H,13C 2D NMR and X-ray studies of the products of the reaction between dibenzylidencyclohexanone and 6-amino-1,3-dimethyl uracil-Reference-Cited by-同舟云学术

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1H,13C 2D NMR and X-ray studies of the products of the reaction between dibenzylidencyclohexanone and 6-amino-1,3-dimethyl uracil

Published:2003-04 Issue:6 Volume:59 Page:1307-1320
ISSN:1386-1425
Container-title:Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
language:en
Short-container-title:Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy

Author:

Dı́az E,Guzmán A,Toscano R.A,Barrios H,Corona D,Fuentes A,Dı́az R,Martinez Zuñiga E.C,Quintero A

Publisher

Elsevier BV

Subject

Spectroscopy,Instrumentation,Atomic and Molecular Physics, and Optics,Analytical Chemistry

Reference20 articles.

1. 2D 1H and 13C NMR evidence for stereoselective formation of a new bond C–N, C–S or C–C in the reaction of ivalin acetate with substituted pyrimidines

2. 2D NMR Studies of the Structures of the Stereoselective Adducts of the Dehydrocostus Lactone with Pyrimidine Derivatives.

3. Stereoselective Michael addition of 6-amino-1,3-dimethyl-2,4-pyrimidinedione to the exocyclic methylene of three sesquiterpene lactones.1H and13C NMR evidence of a new C-C bond and lactam formation

4. Dihalotriphenylphosphoranes in heterocyclic synthesis. Part 8. Reactions of uracils. 6. New ring transformations of 6-aminouracils with acetylenedicarboxylates to pyridinedionates and pyrrolo[3,4-c]pyridines. Some revised constitutions

5. 2D1H and13C NMR studies of the adducts obtained by cyclostereoselective oligomerization ofα,β‒unsaturated arylidenketones promoted by 6 amino‒1,3‒dimethyl uracil

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Synthesis and Cytotoxic Activity of 2,6-Diarylidenecyclohexanones and their 6-Amino-1,3-dimethyluracil Monoadducts;Letters in Drug Design & Discovery;2018-08-27

2. The products of the reaction between 6-amine-1,3-dimethyl uracil and bis-chalcones induce cytotoxicity with massive vacuolation in HeLa cervical cancer cell line;European Journal of Medicinal Chemistry;2013-02

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