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Mendeleev Communications, 1996, Volume 6, Issue 5, Pages 191–193
DOI: https://doi.org/10.1070/MC1996v006n05ABEH000640
(Mi mendc4974)
 

This article is cited in 12 scientific papers (total in 12 papers)

Interaction of P2S5–pyridine with enamines. Synthesis and reactions of l,6-trimethylene-5-cyano-2-mercapto-l,3,2-diazaphosphorine-2-thione

D. B. Nilova, A. V. Kadushkina, N. P. Solov'evaa, A. L. Sedova, V. G. Granikb

a Centre for Medicinal Chemistry. Sergo Ordzhonikidze All-Russian Research Chemical-Pharmaceutical Institute, Moscow, Russian Federation
b Russian Research Centre 'Research Institute of Organic Intermediates and Dyes', Moscow, Russian Federation
Abstract: A new synthesis of l,6-trimethylene-5-cyano-2-mercapto-l,3,2-diazaphosphorine-2,4-dithione (by treatment of enamines with phosphorus pentasulfide in the presence of pyridine) has been developed and some of its reactions are discussed.
Document Type: Article
Language: English


Citation: D. B. Nilov, A. V. Kadushkin, N. P. Solov'eva, A. L. Sedov, V. G. Granik, “Interaction of P2S5–pyridine with enamines. Synthesis and reactions of l,6-trimethylene-5-cyano-2-mercapto-l,3,2-diazaphosphorine-2-thione”, Mendeleev Commun., 6:5 (1996), 191–193
Linking options:
  • https://www.mathnet.ru/eng/mendc4974
  • https://www.mathnet.ru/eng/mendc/v6/i5/p191
  • This publication is cited in the following 12 articles:
    1. V. V. Dotsenko, V. A. Dushenko, N. A. Aksenov, I. V. Aksenova, E. E. Netreba, “Unexpected Result of Thiophosphorylation of 6-Aminopyrano[2,3-c]pyrazole-5-carbonitrile Derivative”, Russ J Gen Chem, 89:9 (2019), 1752  crossref
    2. Victor V. Dotsenko, Vladimir A. Dushenko, Nikolai A. Aksenov, Inna V. Aksenova, Evgeniy E. Netreba, 22nd International Electronic Conference on Synthetic Organic Chemistry, 2018, 26  crossref
    3. Tarik E. Ali, Mohamed A. Assiri, Somaia M. Abdel-Kariem, Ibrahim S. Yahia, “Facile synthesis of novel 6-methyl-5-phenyl-2-sulfido-1,2,3,5-tetrahydro-4H[1,2] oxazolo[4′,5′:5,6]pyrano[2,3-d][1,3,2]diazaphosphinines”, Journal of Sulfur Chemistry, 39:5 (2018), 472  crossref
    4. Tarik E. Ali, Mamdouh M. Ali, Somaia M. Abdel-Kariem, Marwa M. Ahmed, “Reaction of 2-cyano[(4-oxo-4H-chromen-3-yl)methylidene]acetohydrazide with phosphorus reagents: Synthesis and evaluation of anticancer activities of some novel 1,2-azaphospholes, 1,2,3-diazaphospholidine, and 1,3,2-diaza-phosphinanes bearing a chromone ring”, Synthetic Communications, 47:16 (2017), 1458  crossref
    5. Sarra Hichri, Raoudha Abderrahim, “A Convenient Synthesis of 1,3,2-Benzodiazaphophorine-2-oxide”, Phosphorus, Sulfur, and Silicon and the Related Elements, 190:1 (2015), 29  crossref
    6. Turan Ozturk, Erdal Ertas, Olcay Mert, “A Berzelius Reagent, Phosphorus Decasulfide (P4S10), in Organic Syntheses”, Chem. Rev., 110:6 (2010), 3419  crossref
    7. M.-G. A. Shvekhgeimer, “Five-, Six-, and Seven-membered Lactim Ethers. Methods of Synthesis and Chemical Properties. (Review)”, Chem Heterocycl Compd, 41:5 (2005), 551  crossref
    8. D. B. Nilov, V. G. Granik, “Synthesis and properties of benzo[b]thiopheno[2,3-d]-1,3,2λ5-diazaphosphinane-2-thione derivatives”, Mendeleev Commun., 13:2 (2003), 78–79  mathnet  crossref
    9. Gottfried Maerkl, Peter Kreitmeier, Phosphorus-Carbon Heterocyclic Chemistry, 2001, 535  crossref
    10. Vladimir G. Granik, Vadim A. Makarov, Cyril Párkányi, Advances in Heterocyclic Chemistry, 72, Advances in Heterocyclic Chemistry Volume 72, 1998, 283  crossref
    11. D. B. Nilov, N. P. Solov'eva, I. S. Nikolaeva, V. V. Peters, L. Yu. Krylova, T. A. Gus'kova, V. G. Granik, “Synthesis and antiviral activity of pyrazolo[3,4-d]-1,3,2-diazaphosphorins”, Pharm Chem J, 32:7 (1998), 358  crossref
    12. D. B. NILOV, A. V. KADUSHKIN, N. P. SOLOV'EVA, A. L. SEDOV, V. G. GRANIK, “ChemInform Abstract: Interaction of P2S5‐Pyridine with Enamines. Synthesis and Reactions of 1,6‐Trimethylene‐5‐cyano‐2‐mercapto‐1,3,2‐diazaphosphorine‐2‐thione.”, ChemInform, 28:9 (1997)  crossref
    Citing articles in Google Scholar: Russian citations, English citations
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