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Pure Appl. Chem., 1999, Vol. 71, No. 4, pp. 587-643

http://dx.doi.org/10.1351/pac199971040587

ORGANIC CHEMISTRY DIVISION
COMMISSION ON NOMENCLATURE OF ORGANIC CHEMISTRY

Revised Section F: Natural products and related compounds

P. M. Giles, Jr.

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  • Cmoch Piotr, Korda Anna, Rárová Lucie, Oklešťková Jana, Strnad Miroslav, Luboradzki Roman, Pakulski Zbigniew: Synthesis and structure–activity relationship study of cytotoxic lupane-type 3β-O-monodesmosidic saponins with an extended C-28 side chain. Tetrahedron 2014, 70, 2717. <http://dx.doi.org/10.1016/j.tet.2014.03.006>
  • Morin James G.: Based on a review of the data, use of the term ‘cypridinid’ solves the Cypridina/Vargula dilemma for naming the constituents of the luminescent system of ostracods in the family Cypridinidae. formerly the Journal of Bioluminescence and Chemiluminescence 2011, 26, 1. <http://dx.doi.org/10.1002/bio.1178>
  • Kataev E., Khaybullin R. N., Sharipova R. R., Strobykina I. Yu.: Ent-kaurane diterpenoids and glycosides: Isolation, properties, and chemical transformations. Ref J Chem 2011, 1, 93. <http://dx.doi.org/10.1134/S2079978011010043>
  • Ye Haoyu, Zhong Shijie, Li Yanfang, Tang Minghai, Peng Aihua, Hu Jia, Shi Jie, He Shicao, Wu Wenshuang, Chen Lijuan: Enrichment and isolation of barbigerone from Millettia pachycarpa Benth. using high-speed counter-current chromatography and preparative HPLC. J Sep Science 2010, NA. <http://dx.doi.org/10.1002/jssc.200900641>
  • Salvador Jorge A. R., Pinto Rui M. A., Santos Rita C., Le Roux Christophe, Beja Ana Matos, Paixão José A.: Bismuth triflate-catalyzed Wagner-Meerwein rearrangement in terpenes. Application to the synthesis of the 18α-oleanane core and A-neo-18α-oleanene compounds from lupanes. Org Biomol Chem 2009, 7, 508. <http://dx.doi.org/10.1039/b814448f>
  • Schomburg Dietmar: Nomenklatur der Lignane und Neolignane. Angew Chem 2005, 117, 2339. <http://dx.doi.org/10.1002/ange.200462947>
  • Thilgen Carlo: Nomenklatur der Fullerene C60-Ih und C70-D5h(6). Angew Chem 2005, 117, 5065. <http://dx.doi.org/10.1002/ange.200501717>
  • Zhang Hong-Jie, Tan Ghee Teng, Hoang Vu Dinh, Hung Nguyen Van, Cuong Nguyen Manh, Soejarto Djaja Doel, Pezzuto John M, Fong Harry H.S: Natural anti-HIV agents. Part 2: Litseaverticillol A, a prototypic litseane sesquiterpene from Litsea verticillata. Tetrahetron Lett 2001, 42, 8587. <http://dx.doi.org/10.1016/S0040-4039(01)01852-4>