Alkaloids from an algicolous strain of Talaromyces sp.

• Batishta J M, Batista A N L, Rinaldo D, Vilegas W, Ambrósio D L, Cicarelli R M B, Bolzani V S, Kato M J, Nafie L A, López S N, Furlan M. 2011. Absolute configuration and selective trypanocidal activity of gaudichaudianic acid enantiomers. J. Nat. Prod., 74 (5): 1154–1160.

  Article  Google Scholar 

• Bruhn T, Schaumlöffel A, Hemberger Y, Bringmann G. 2013. SpecDis: quantifying the comparison of calculated and experimental electronic circular dichroism spectra, Version 1.62. Chirality, 25: 243–249, http://www-organik. chemie.uni-wuerzburg.de/lehrstuehlearbeitskreise/bringmann/specdis. Accessed on 2013-10-05.

  Article  Google Scholar 

• Catir M, Cakici M, Karabuga S, Ulukanli S, Sahin E, Kilic H. 2009. Synthesis of 4, 4’-biquinazoline alcohols as chiral catalysts in enantioselective alkynylation of aldehydes with phenyl acetylene. Tetrahedron: Asymmetry, 20 (24): 2845–2853.

  Article  Google Scholar 

• Fan Y Q, Wang Y, Liu P P, Fu P, Zhu T H, Wang W, Zhu W M. 2013. Indole-diterpenoids with anti-H1N1 activity from the aciduric fungus Penicillium camemberti OUCMDZ-1492. J. Nat. Prod., 76 (7): 1328–1336.

  Article  Google Scholar 

• Fremlin L J, Piggott A M, Lacey E, Capon R J. 2009. Cottoquinazoline A and cotteslosins A and B, metabolites from an Australian marine-derived strain of Aspergillus versicolor. J. Nat. Prod., 72 (4): 666–670.

  Article  Google Scholar 

• Frisch M J, Trucks G W, Schlegel H B, Scuseria G E, Robb M A, Cheeseman J R, Scalmani G, Barone V, Mennucci B, Petersson G A, et al. 2010. Gaussian 09, Revision C. 01. http://www.gaussian.com/g_prod/g09.htm. Accessed on 2014-02-23.

  Google Scholar 

• Itabashi T, Hosoe T, Wakana D, Fukushima K, Takizawa K, Yaguchi T, Okada K, De Campos Takaki G M, Kawai K. 2009. A new indoloditerpene derivative, penijanthine A, isolated from Penicillium janthinellum. J. Nat. Med., 63 (1): 96–99.

  Article  Google Scholar 

• Ji N Y, Liang X R, Sun R R, Miao F P. 2014. A rule to distinguish diastereomeric bianthrones by 1 H NMR. RSC Adv., 4 (15): 7710–7715.

  Article  Google Scholar 

• Ji N Y, Liu X H, Miao F P, Qiao M F. 2013. Aspeverin, a new alkaloid from an algicolous strain of Aspergillus versicolor. Org. Lett., 15 (10): 2327–2329.

  Article  Google Scholar 

• Li X D, Miao F P, Liang X R, Wang B G, Ji N Y. 2013. Two halosesquiterpenes from Laurencia composita. RSC Adv., 3 (6): 1953–1956.

  Article  Google Scholar 

• MarvinSketch with calculator plugins for structure property prediction and calculation. 2014. ChemAxon, Marvin 6.2.2. http://www.chemaxon.com. Accessed on 2014-04-19.

  Google Scholar 

• Mazzeo G, Santoro E, Andolfi A, Cimmino A, Troselj P, Petrovic A G, Superchi S, Evidente A, Berova N. 2013. Absolute configurations of fungal and plant metabolites by chiroptical methods. ORD, ECD, and VCD studies on phyllostin, scytolide, and oxysporone. J. Nat. Prod., 76 (4): 588–599.

  Article  Google Scholar 

• Miao F P, Liang X R, Liu X H, Ji N Y. 2014. Aspewentins A-C, norditerpenes from a cryptic pathway in an algicolous strain of Aspergillus wentii. J. Nat. Prod., 77 (2): 429–432.

  Article  Google Scholar 

• Miao F P, Liang X R, Yin X L, Wang G, Ji N Y. 2012. Absolute configurations of unique harziane diterpenes from Trichoderma species. Org. Lett., 14 (15): 3815–3817.

  Article  Google Scholar 

• Musuku A, Selala M I, De Bruyne T, Claeys M, Schepens P J C, Tsatsakis A, Shtilman M I. 1994. Isolation and structure determination of a new roquefortine-related mycotoxin from Penicillium v errucosum var. cyclopium isolated from cassava. J. Nat. Prod., 57 (7): 983–987.

  Article  Google Scholar 

• Nozawa K, Nakajima S, Kawai K, Udaqawa S. 1988. Isolation and structures of indoloditerpenes, possible biosynthetic intermediates to the tremorgenic mycotoxin, paxilline, from Emericella s t riata. J. Chem. Soc., Perkin Trans., 1 (9): 2607–2610.

  Article  Google Scholar 

• Rufino A T, Ribeiro M, Judas F, Salgueiro L, Lopes M C, Cavaleiro C, Mendes A F. 2014. Anti-inflammatory and chondroprotective activity of (+)-a-pinene: structural and enantiomeric selectivity. J. Nat. Prod., 77 (2): 264–269.

  Article  Google Scholar 

• Rundberget T, Wilkins A L. 2002. Thomitrems A and E, two indole-alkaloid isoprenoids from Penicillium crustosum Thom. Phytochemistry, 61 (8): 979–985.

  Article  Google Scholar 

• Santoro S, Superchi S, Messina F, Santoro E, Rosati O, Santi C, Marcotullio M C. 2013. Agarsenone, a cadinane sesquiterpenoid from Commiphora erythraea. J. Nat. Prod., 76 (7): 1254–1259.

  Article  Google Scholar 

• Scott P M, Polonsky J, Merrien M A. 1979. Configuration of the 3, 12 double bond of roquefortine. J. Agric. Food Chem., 27 (1): 201–202.

  Article  Google Scholar 

• Stephens P J, Pan J J, Devlin F J, Cheeseman J R. 2008a. Determination of the absolute configurations of natural products using TDDFT optical rotation calculations: the iridoid oruwacin. J. Nat. Prod., 71 (2): 285–288.

  Article  Google Scholar 

• Stephens P J, Pan J J, Devlin F J, Urbanová M, Julínek O, Hájícek J. 2008b. Determination of the absolute configurations of natural products via density functional theory calculations of vibrational circular dichroism, electronic circular dichroism, and optical rotation: the isoschizozygane alkaloids isoschizogaline and isoschizogamine. Chirality, 20 (3-4): 454–470.

  Article  Google Scholar 

• Tennant G. 1966. The chemistry of polyazaheterocyclic compounds. Part 1. The structure and reactivity of the 1, 2, 3-triazolo[1, 5-a ]quinazoline ring system. J. Chem. Soc. (C), 2 290–2 295.

  Google Scholar 

• Wu R B, Cheng Z B, Han Q H, Lin T T, Zhou J W, Tang G H, Yin S. 2014. Determination of the absolute stereochemistry of two new aristophyllene sesquiterpenes: a combined theoretical and experimental investigation. Chirality, 26 (4): 189–193.

  Article  Google Scholar 

Download references