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J. CHEM. SOC. PERKIN TRANS. 1 1994 Corrigenda Synthesis of 12-Oxophytodienoic Acid (12-oxoPDA) and the Compounds of its Enzymic Degradation Cascade in Plants, OPC-8 :0, -6:0, -4:0 and -2 :0 (epi-Jasmonic acid), as their Methyl Esters Leslie Crombie and Kamlesh M. Mistry J. Chem. SOC.,Perkin Trans. 1, 1991. 1981 Page 1989, left-hand column, compound 32,3rd line: delete ‘m.p. 68-69 OC’ and insert ‘1 14-1 15 OC’. Unexpected Formation and Crystal Structure of a Spiroindene-I ,7’(6‘H)-pyrrolo3,4-61 pyridin-5’-one Abood A. Bahajaj, Gregory J. Hitchings, Madeleine H. Moore and John M. Vernon J. Chem. SOC..Perkin Trans. 7, 1994, 121 1 Page 12 1 1, left-hand column, formulae 5a, b and 6a, b: delete displayed formula and insert: 0 Palladium-catalysed Carbocyclization of Organophosphorus Compounds: A Novel and Effective Method for the Synthesis of Cyclic Organophosphorus Compounds Including the Phosphorus Analogues of a-Methylene Lactones Feng Hong, Jiazhi Xia and Yuanyao Xu J.Chem. SOC.,Perkin Trans. 1, 1994, 1665 Page 1666, Table 1: delete formula 3f and replace by: 31 3600 J. CHEM. SOC. PERKIN TRANS. 1 1994 Pheromone Synthesis. Part 166. Synthesis of (2€,5R,6€,8€)-5,7-DimethyI-deca-2,6,8-trien-4-one, the Major Component of the Sex Pheromone of the Israeli Pine Bast Scale, and Its Antipode Kenji Mori" and Masayasu Amaiket J. Chem. SOC..Perkin Trans. I, 1994, 2727 Page 2728, Scheme 3: delete structures 14 and 15 and insert the following: OTBS OTBS OHC*cHo 14 15(=B) Stereochemistry of the Baker's Yeast Mediated Reduction of the C=C Bond of (Z)-and (E)-5-Benzoyloxyhex-S-en-2-one Giovanni Fronza, Claudio Fuganti, Piero Grasselli, Simonetta Lanati, Roberta Rallo and Susanna Tchilibon J. Chem. SOC..Perkin Trans. 1. 1994, 2927 Page 2927, left-hand column, formulae 3,3a: delete displayed formula and insert: Page 2928, left-hand column, formulae 10 and 16:delete displayed formulae and insert: 10 6 0Copyright 1994 by the Royal Society of Chemistry
机译:J. CHEM. SOC. PERKIN TRANS. 1 1994 12-氧代植物二烯酸 (12-oxoPDA) 及其酶降解级联化合物的更正,OPC-8 :0, -6:0, -4:0 和 -2 :0(epi-茉莉酸),作为他们的甲酯 Leslie Crombie 和 Kamlesh M. Mistry J. Chem. SOC.,Perkin Trans. 1, 1991.1981年,第1989页,左栏,第32号复合体第3行:删去“m.p.68-69 OC”,插入“1 14-1 15 OC”。螺[茚-I,7'(6'H)-吡咯并[3,4-61吡啶]-5'-酮的意外形成和晶体结构 Abood A. Bahajaj, Gregory J. Hitchings, Madeleine H. Moore 和 John M. Vernon J. Chem. SOC..Perkin Trans. 7, 1994, 121 1 第 12 页 1 1,左栏,式 5a、b 和 6a、b:删除显示的公式并插入: 0 钯催化的有机磷化合物碳环化:一种合成环状有机磷化合物的新方法,包括 α-亚甲基内酯的磷类似物 冯红、夏佳志、徐元尧 J.Chem. SOC.,Perkin Trans. 1, 1994, 1665 Page 1666, Table 1: 删除式3f,代之以: 31 3600 J. CHEM. SOC. PERKIN TRANS. 1 1994 Pheromone Synthesis.第166部分。(2€,5R,6€,8€)-5,7-二甲基I-癸-2,6,8-三烯-4-酮的合成,以色列松树基鳞片性信息素的主要成分及其对立面Kenji Mori“和Masayasu Amaiket J. Chem. SOC.。珀金译。I, 1994, 2727 Page 2728, 方案 3:删除结构 14 和 15 并插入以下内容: OTBS OTBS OHC*cHo 14 15(=B) 贝克酵母的立体化学介导的 C=C 键的还原 (Z) 和 (E)-5-苯甲酰氧基己-S-烯-2-酮 Giovanni Fronza、Claudio Fuganti、Piero Grasselli、Simonetta Lanati、Roberta Rallo 和 Susanna Tchilibon J. Chem. SOC..珀金译 1.1994, 2927 第 2927 页,左栏,公式 3,3a:删除显示的公式并插入:第 2928 页,左栏,公式 10 和 16:删除显示的公式并插入:10 6 0194 年英国皇家化学学会版权所有

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