메뉴 건너뛰기




Volumn 17, Issue 2, 2012, Pages 1675-1685

Multicomponent synthesis of 3,6-Dihydro-2H-1,3-thiazine-2-thiones

Author keywords

1 azadiene; 3,6 dihydro 2H 1,3 thiazine 2 thiones; Carbon disulfide; Cyclic dithiocarbamates; Molecular complexity; Multi component reactions

Indexed keywords

THIAZINE DERIVATIVE; THIOKETONE;

EID: 84857621780     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules17021675     Document Type: Article
Times cited : (20)

References (24)
  • 1
    • 79959907066 scopus 로고    scopus 로고
    • Multicomponent reaction design in the quest for molecular complexity and diversity
    • Ruijter, E.; Scheffelaar, R.; Orru, R.V.A. Multicomponent reaction design in the quest for molecular complexity and diversity. Angew. Chem. Int. Ed. 2011, 50, 6234-6246.
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 6234-6246
    • Ruijter, E.1    Scheffelaar, R.2    Orru, R.V.A.3
  • 5
    • 13744252141 scopus 로고    scopus 로고
    • One-pot synthesis of polysubstituted pyrimidines
    • DOI 10.1016/j.tetlet.2005.01.068
    • Kiselyov, A.S. One-pot synthesis of polysubstituted pyrimidines. Tetrahedron Lett. 2005, 46, 1663-1665. (Pubitemid 40238685)
    • (2005) Tetrahedron Letters , vol.46 , Issue.10 , pp. 1663-1665
    • Kiselyov, A.S.1
  • 6
    • 55849150974 scopus 로고    scopus 로고
    • 1-Azadienes in cycloaddition and multicomponent reactions towards N-heterocycles
    • Groenendaal, B.; Ruijter, E.; Orru, R.V.A. 1-Azadienes in cycloaddition and multicomponent reactions towards N-heterocycles. Chem. Commun. 2008, 5474-5489.
    • (2008) Chem. Commun. , pp. 5474-5489
    • Groenendaal, B.1    Ruijter, E.2    Orru, R.V.A.3
  • 8
    • 0010312097 scopus 로고
    • A novel synthesis of β-trichlorostannyl ketones from siloxycyclopropanes and their facile dehydrostannation affording 2-methylene ketones
    • Ryu, I.; Murai, S.; Sonoda, N. A novel synthesis of β- trichlorostannyl ketones from siloxycyclopropanes and their facile dehydrostannation affording 2-methylene ketones. J. Org. Chem. 1986, 51, 2389-2391.
    • (1986) J. Org. Chem. , vol.51 , pp. 2389-2391
    • Ryu, I.1    Murai, S.2    Sonoda, N.3
  • 9
    • 70749084818 scopus 로고    scopus 로고
    • Living radical polymerization by the RAFT process - A second update
    • Moad, G.; Rizzardo, E.; Thang, S.H. Living radical polymerization by the RAFT process - A second update. Aust. J. Chem. 2009, 62, 1402-1472.
    • (2009) Aust. J. Chem. , vol.62 , pp. 1402-1472
    • Moad, G.1    Rizzardo, E.2    Thang, S.H.3
  • 10
    • 73649099477 scopus 로고    scopus 로고
    • Efficiency of alkoxyl radical product formation from 5-substituted 3-alkoxy-4-methylthiazole-2(3H)-thiones
    • Hartung, J.; Schur, C.; Kempter, I.; Gottwald, T. Efficiency of alkoxyl radical product formation from 5-substituted 3-alkoxy-4-methylthiazole-2(3H)- thiones. Tetrahedron 2010, 66, 1365-1374.
    • (2010) Tetrahedron , vol.66 , pp. 1365-1374
    • Hartung, J.1    Schur, C.2    Kempter, I.3    Gottwald, T.4
  • 11
    • 79952144808 scopus 로고    scopus 로고
    • Treasures from the free radical renaissance period- Miscellaneous hexenyl radical kinetic data
    • Beckwith, A.L.J.; Schiesser, C.H. Treasures from the free radical renaissance period- Miscellaneous hexenyl radical kinetic data. Org. Biomol. Chem. 2011, 9, 1736-1743.
    • (2011) Org. Biomol. Chem. , vol.9 , pp. 1736-1743
    • Beckwith, A.L.J.1    Schiesser, C.H.2
  • 13
    • 34047188045 scopus 로고    scopus 로고
    • Synthesis and antihypertensive activity of novel 3-benzyl-2-substituted- 3H-[1,2,4]triazolo[5,1-b]quinazolin-9-ones
    • DOI 10.1016/j.bmc.2007.03.007, PII S0968089607001939
    • Alagarsamy, V.; Pathak, U.S. Synthesis and antihypertensive activity of novel 3-benzyl-2- substituted-3H-[1,2,4]triazolo[5,1-b]quinazolin-9-ones. Bioorg. Med. Chem. 2007, 15, 3457-3462. (Pubitemid 46529260)
    • (2007) Bioorganic and Medicinal Chemistry , vol.15 , Issue.10 , pp. 3457-3462
    • Alagarsamy, V.1    Pathak, U.S.2
  • 14
    • 37849005301 scopus 로고    scopus 로고
    • Dithiocarbamate and CuO promoted one-pot synthesis of 2-(N-substituted)-aminobenzimidazoles and related heterocycles
    • Das, P.; Kumar, C.K.; Kumar, K.N.; Innus, M.; Iqbal, J.; Srinivas, N. Dithiocarbamate and CuO promoted one-pot synthesis of 2-(N-substituted)- aminobenzimidazoles and related heterocycles. Tetrahedron Lett. 2008, 49, 992-995.
    • (2008) Tetrahedron Lett. , vol.49 , pp. 992-995
    • Das, P.1    Kumar, C.K.2    Kumar, K.N.3    Innus, M.4    Iqbal, J.5    Srinivas, N.6
  • 15
    • 77955669542 scopus 로고    scopus 로고
    • Synthesis and tuberculostatic activity of novel 1,2,4-triazoles obtained from heterocyclic carbohydrazides
    • Gobis, K.; Foks, H.; Zwolska, Z.; Augustynowicz-Kope, E. Synthesis and tuberculostatic activity of novel 1,2,4-triazoles obtained from heterocyclic carbohydrazides. Heterocycles 2010, 81, 917-934.
    • (2010) Heterocycles , vol.81 , pp. 917-934
    • Gobis, K.1    Foks, H.2    Zwolska, Z.3    Augustynowicz-Kope, E.4
  • 16
    • 25144447819 scopus 로고
    • Addition of dithiocarbaminic acid to alpha,betaunsaturated aldehydes and ketones - Simple synthesis of 4-alkoxytertrahydro-1,3-thiazine-2- thiones
    • Shutalev, A.D.; Pagaev, M.T.; Ignatova, L.A. Addition of dithiocarbaminic acid to alpha,betaunsaturated aldehydes and ketones - Simple synthesis of 4-alkoxytertrahydro-1,3-thiazine-2- thiones. Zh. Org. Khim. 1991, 27, 1274-1285.
    • (1991) Zh. Org. Khim. , vol.27 , pp. 1274-1285
    • Shutalev, A.D.1    Pagaev, M.T.2    Ignatova, L.A.3
  • 17
    • 0037907819 scopus 로고
    • Some thiazinethiols and their intermediate compounds
    • Jansen, J.E.; Mathes, R.A. Some thiazinethiols and their intermediate compounds. J. Am. Chem. Soc. 1955, 77, 2866.
    • (1955) J. Am. Chem. Soc. , vol.77 , pp. 2866
    • Jansen, J.E.1    Mathes, R.A.2
  • 18
    • 84857588147 scopus 로고
    • Communication 2. Alkylation of some heterocyclic compounds by derivatives of phosphoric and phosphourous acids
    • Arbusow, B.A.; Soroastrowa, V.M. Communication 2. Alkylation of some heterocyclic compounds by derivatives of phosphoric and phosphourous acids. Russ. Chem. Bull. 1959, 1001-1004.
    • (1959) Russ. Chem. Bull. , pp. 1001-1004
    • Arbusow, B.A.1    Soroastrowa, V.M.2
  • 19
    • 37049040108 scopus 로고
    • Cyclic derivatives of dithiocarbamic acids
    • Garraway, J.L. Cyclic derivatives of dithiocarbamic acids. J. Chem. Soc. 1964, 760, 4008-4011.
    • (1964) J. Chem. Soc. , vol.760 , pp. 4008-4011
    • Garraway, J.L.1
  • 20
    • 0004968781 scopus 로고
    • Synthesis of 4,6-diaryl-2,3-dihydro-6H-1,3-thiazine-2-thiones by the reaction of chalcones with dithiocarbamic acid
    • Perjesi, P.; Szabo, D.; Foldesi, A. Synthesis of 4,6-diaryl-2,3-dihydro- 6H-1,3-thiazine-2-thiones by the reaction of chalcones with dithiocarbamic acid. Acta Chim. Hung. 1986, 122, 119-125.
    • (1986) Acta Chim. Hung. , vol.122 , pp. 119-125
    • Perjesi, P.1    Szabo, D.2    Foldesi, A.3
  • 21
    • 0026035165 scopus 로고
    • One-pot synthesis of α,β-unsaturated ketones
    • Lee, K.; Oh, D.Y. One-pot synthesis of α,β-unsaturated ketones. Synthesis 1991, 1991, 213-214.
    • (1991) Synthesis , vol.1991 , pp. 213-214
    • Lee, K.1    Oh, D.Y.2
  • 22
    • 0028814403 scopus 로고
    • One-pot synthesis of primary E-allylic amines
    • Shin, W.S.; Lee, K.; Oh, D.Y. One-pot synthesis of primary E-allylic amines. Tetrahedron Lett. 1995, 36, 281-282.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 281-282
    • Shin, W.S.1    Lee, K.2    Oh, D.Y.3
  • 24
    • 84857547930 scopus 로고    scopus 로고
    • The base peak in all HRMS spectra represents the 1-azadiene, e.g., the product-CS2. This is most likely due to better ionizability of the 1-azadiene combined with the entropic benefit of the formal retro-hetero-Diels-Alder reaction under ESI conditions
    • The base peak in all HRMS spectra represents the 1-azadiene, e.g., the product-CS2. This is most likely due to better ionizability of the 1-azadiene combined with the entropic benefit of the formal retro-hetero-Diels-Alder reaction under ESI conditions.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.