Eschew 发表于 2025-3-21 19:05:22
书目名称Asymmetric Synthesis of Bioactive Lactones and the Development of a Catalytic Asymmetric Synthesis o影响因子(影响力)<br> http://figure.impactfactor.cn/if/?ISSN=BK0163755<br><br> <br><br>书目名称Asymmetric Synthesis of Bioactive Lactones and the Development of a Catalytic Asymmetric Synthesis o影响因子(影响力)学科排名<br> http://figure.impactfactor.cn/ifr/?ISSN=BK0163755<br><br> <br><br>书目名称Asymmetric Synthesis of Bioactive Lactones and the Development of a Catalytic Asymmetric Synthesis o网络公开度<br> http://figure.impactfactor.cn/at/?ISSN=BK0163755<br><br> <br><br>书目名称Asymmetric Synthesis of Bioactive Lactones and the Development of a Catalytic Asymmetric Synthesis o网络公开度学科排名<br> http://figure.impactfactor.cn/atr/?ISSN=BK0163755<br><br> <br><br>书目名称Asymmetric Synthesis of Bioactive Lactones and the Development of a Catalytic Asymmetric Synthesis o被引频次<br> http://figure.impactfactor.cn/tc/?ISSN=BK0163755<br><br> <br><br>书目名称Asymmetric Synthesis of Bioactive Lactones and the Development of a Catalytic Asymmetric Synthesis o被引频次学科排名<br> http://figure.impactfactor.cn/tcr/?ISSN=BK0163755<br><br> <br><br>书目名称Asymmetric Synthesis of Bioactive Lactones and the Development of a Catalytic Asymmetric Synthesis o年度引用<br> http://figure.impactfactor.cn/ii/?ISSN=BK0163755<br><br> <br><br>书目名称Asymmetric Synthesis of Bioactive Lactones and the Development of a Catalytic Asymmetric Synthesis o年度引用学科排名<br> http://figure.impactfactor.cn/iir/?ISSN=BK0163755<br><br> <br><br>书目名称Asymmetric Synthesis of Bioactive Lactones and the Development of a Catalytic Asymmetric Synthesis o读者反馈<br> http://figure.impactfactor.cn/5y/?ISSN=BK0163755<br><br> <br><br>书目名称Asymmetric Synthesis of Bioactive Lactones and the Development of a Catalytic Asymmetric Synthesis o读者反馈学科排名<br> http://figure.impactfactor.cn/5yr/?ISSN=BK0163755<br><br> <br><br>Harpoon 发表于 2025-3-21 23:52:27
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M. Ataharul Islam,Abdullah Al-Shihaylative protonation of the corresponding α-aryl-β-keto allyl esters. Enantioselectivities of up to 92 % . and 74 % . were achieved for cyclopentanone and cyclohexanone substrates, respectively. The route described gives access to these important structural motifs in moderate to high levels of enanti释放 发表于 2025-3-22 17:52:46
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,Introduction to the Development of a Catalytic Asymmetric Synthesis of Tertiary α-Aryl Ketones,Biological systems recognise a pair of enantiomers as different substances and thus each enantiomer will trigger a different response. It is possible that one enantiomer could act positively as a therapeutic agent and the other enantiomer might be very harmful or toxic.entice 发表于 2025-3-23 03:09:32
Robert DoranNominated as an outstanding Ph.D. thesis by University College Dublin, Ireland.Outlines the synthesis of a new bioactive lactone-containing natural product analog.Describes the development of a cataly流逝 发表于 2025-3-23 06:30:10
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