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Number of items: 17.

A

Appleton, D.R. and Pearce, A.N. and Copp, B.R. (2010) Anti-Tuberculosis natural products: synthesis and biological evaluation of pyridoacridine alkaloids related to ascididemin. Tetrahedron, 66 (27-28). pp. 4977-4986.

Arshad, Ahmad Saifuddin Mohamad and Meesala, Ramu and Hanapi, Nur Aziah and Mordi, Mohd Nizam (2021) A convenient synthesis of beta-carbolines by iron-catalyzed aerobic decarboxylative/dehydrogenative aromatization of tetrahydro-beta-carbolines under air. Tetrahedron, 83. ISSN 0040-4020, DOI https://doi.org/10.1016/j.tet.2021.131960.

D

Dumontet, V. and Thoison, O. and Olamrewaju, R.O. and Martin, Marie-Thérèse and Hamid, A.H.A. and Guillaume, P. and Angèle, C. and Claude, R. and Mary, P. and Thierry, S. (1996) New nitrogenous and aromatic derivatives from Aglaia argentea and A. forbesii. Tetrahedron, 52 (20). pp. 6931-6942. ISSN 00404020, DOI https://doi.org/10.1016/0040-4020(96)00322-5.

K

Kam, T.S. and Tan, S.J. and Robinson, W.T. and Komiyama, K. (2011) Macrodasines A—G, macroline indole alkaloids incorporating fused spirocyclic tetrahydrofuran—tetrahydrofuran and tetrahydrofuran—tetrahydropyran rings. Tetrahedron, 67. pp. 3830-3838. ISSN 0040-4020, DOI https://doi.org/10.1016/j.tet.2011.03.099.

Kam, Toh Seok and Tan, S.J. and Choo, Y.M. and Thomas, N.F. and Robinson, W.T. and Komiyama, K. (2012) Unusual indole alkaloid—epyrrole, —epyrone, and —carbamic acid adducts from Alstonia angustifolia. Tetrahedron, 66. pp. 7799-7806. ISSN 0040-4020, DOI https://doi.org/10.1016/j.tet.2010.07.079.

Khoo, L. and Lee, H.H. (1970) Hydrostannolysis reactions—II Reaction of phenolic esters with tri-n-butyltin hydride. Tetrahedron, 26 (18). pp. 4261-4268. ISSN 00404020, DOI https://doi.org/10.1016/S0040-4020(01)93069-8.

Khoo, L.E. and Lee, H.H. (1970) Hydrostannolysis reactions-II. Reaction of phenolic esters with tri-n-butyltin hydride. Tetrahedron, 26 (18). pp. 4261-4268. ISSN 0040-4020, DOI https://doi.org/10.1016/S0040-4020(01)93069-8.

L

Lee, K.H. (1968) Polar effects in hydrogen abstraction from benzaldehydes—I. Tetrahedron, 24 (13). pp. 4793-4803. ISSN 0040-4020, DOI https://doi.org/10.1016/S0040-4020(01)98675-2.

Lee, Kheng H. (1970) Polar effects in hydrogen abstraction from benzaldehydes—II : Radical chlorination by CCl3SO2Cl. Tetrahedron, 26 (5). pp. 1503-1507. ISSN 0040-4020, DOI https://doi.org/10.1016/S0040-4020(01)92979-5.

Lee, Kheng H. (1970) Polar effects in hydrogen abstraction from benzaldehydes—III : Radical chlorination by sulphuryl chloride. Tetrahedron, 26 (8). pp. 2041-2044. ISSN 0040-4020, DOI https://doi.org/10.1016/S0040-4020(01)92779-6.

N

Nugroho, M.E. and Momota, T. and Sugiura, R. and Hanzawa, M. and Yajima, E. and Nagakura, Y. and Yasuda, N. and Hirasawa, Y. and Wong, C.P. and Kaneda, T. and Hadi, A.H.A. and Fukaya, H. and Morita, H. (2014) Dysotriflorins A-M, triterpenoids from dysoxylum densiflorum. Tetrahedron, 70 (51). pp. 9661-9667.

S

Sperátová, Michaela and Jedyrka, Jaroslaw and Pytela, Oldřich and Kityk, Iwan V. and Reshak, Ali H. and Bureš, Filip and Klikar, Milan (2019) Novel dibenzothiophene chromophores with peripheral barbituric acceptors. Tetrahedron, 75 (34). p. 130459. ISSN 0040-4020, DOI https://doi.org/10.1016/j.tet.2019.07.017.

T

Tan, Shin-Jowl and Choo, Yeun-Mun and Thomas, N.F. and Robinson, W.T. and Komiyama, K. and Kam, Toh-Seok (2010) Unusual indole alkaloid-pyrrole, -pyrone, and -carbamic acid adducts from Alstonia angustifolia. Tetrahedron, 66 (39). pp. 7799-7806.

Tan, Siow Ping and Ali, Abdul Manaf and Nafiah, Mohd Azlan and Awang, Khalijah and Ahmad, Kartini (2015) Isolation and cytotoxic investigation of new carbazole alkaloids from Murraya koenigii (Linn.) Spreng. Tetrahedron, 71 (23). pp. 3946-3953. ISSN 0040-4020, DOI https://doi.org/10.1016/j.tet.2015.04.037.

W

Wong, Soon Kit and Yeap, Joanne Soon Yee and Tan, Chun Hoe and Sim, Kae Shin and Lim, Siew Huah and Low, Yun Yee and Kam, Toh Seok (2021) Arbolodinines A−C, biologically-active aspidofractinine-aspidofractinine, aspidofractinine-strychnan, and kopsine-strychnan bisindole alkaloids from Kopsia arborea. Tetrahedron, 78. p. 131802. ISSN 0040-4020, DOI https://doi.org/10.1016/j.tet.2020.131802.

Wong, Soon-Kit and Yeap, Joanne Soon-Yee and Tan, Chun-Hoe and Sim, Kae-Shin and Lim, Siew-Huah and Low, Yun-Yee and Kam, Toh-Seok (2021) Arbolodinines A-C, biologically-active aspidofractinine-aspidofractinine, aspidofractinine-strychnan, and kopsine-strychnan bisindole alkaloids from Kopsia arborea. Tetrahedron, 78. ISSN 0040-4020, DOI https://doi.org/10.1016/j.tet.2020.131802.

Z

Zvarec, O. and Avery, T.D. and Taylor, D.K. and Tiekink, E.R.T. (2010) Cyclisation of 1,2-dioxines containing tethered hydroxyl and carboxylic acid functionality: Synthesis of tetrahydrofurans and dihydrofuran-2(3H)-ones. Tetrahedron, 66 (4). pp. 1007-1013.

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