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Stereoselective Synthesis of α,α‐Chlorofluoro Carbonyl Compounds Leading to the Construction of Fluorinated Chiral Quaternary Carbon Centers

机译：α，α-氯氟烃羰基化合物的立体选择性合成，导致氟化手性季碳中心的构建

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Kazutaka Shibatomi; Hisashi Yamamoto;
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1. Stereoselective Synthesis of alpha,alpha-Chlorofluoro Carbonyl Compounds Leading to the Construction of Fluorinated Chiral Quaternary Carbon Centers [J] . Kazutaka Shibatomi, Hisashi Yamamoto Angewandte Chemie . 2008,第31期

机译：立体选择性合成的α，α-氯氟羰基化合物导致氟化手性季碳中心的建设
2. Stereoselective construction of all-carbon quaternary stereocenters by allylboration of chiral aldehydes: synthesis of a fragment of (+)-vibsanin A [J] . Sakama Akihiro, Nishimura Yoshiyasu, Motohashi Yuko, Tetrahedron . 2016,第35期

机译：通过手性醛的烯丙基硼化全碳四元立体中心的立体选择性构建：（+）-vibsanin A片段的合成
3. Stereoselective construction of quaternary chiral centers using Ti(III)-mediated opening of 2,3-epoxy alcohols: studies directed toward the synthesis of penifulvins [J] . Tushar Kanti Chakraborty, Amit Kumar Chattopadhyay, Rajarshi Samanta Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry . 2010,第33期

机译：使用Ti（III）介导的2，3-环氧醇打开，立体选择性地构筑四元手性中心：针对Penifulvins合成的研究
4. Cationic Rhodium Complex-Catalyzed Hydrosilylation of a,P-Unsaturated Carbonyl Compounds: Stereoselective Synthesis of Acyclic Silyl Enol Ethers [C] . Gen Onodera, Ryosuke Hachisuka, Satoko Kezuka Symposium on Organometallic Chemistry . 2006

机译：阳离子铑络合物催化A，P-不饱和羰基化合物：无环甲硅烷基烯醇醚的立体选择合成
5. Stereoselective formation of all carbon quaternary centers: Synthesis of alpha,alpha-disubstituted beta-amino carbonyl compounds via the Mannich reaction and total synthesis of (-)-puraquinonic acid. [D] . Tiong, Erica Anne. 2011

机译：所有碳四元中心的立体选择性形成：通过曼尼希反应合成α，α-二取代的β-氨基羰基化合物，以及（-）-嘌呤奎尼酸的全合成。
6. Stereoselective Synthesis of αα-Chlorofluoro Carbonyl Compounds Leading to the Construction of Fluorinated Chiral Quaternary Carbon Centers [O] . Kazutaka Shibatomi, Hisashi Yamamoto -1

机译：立体选择性合成αα-氯氟羰基化合物导致氟化手性季碳中心的构建
7. Enantioselective construction of nitrogen-substituted quaternary carbon centers adjacent to the carbonyl group in the cyclohexane ring: first asymmetric synthesis of anesthetic (S)-ketamine with high selectivity [O] . Yokoyama, Reiko, Matsumoto, Satoshi, Nomura, Satoshi, 2009

机译：与环己烷环中羰基相邻的氮取代的季碳中心的对映选择性结构：麻醉性（S）-氯胺酮的高选择性第一合成反应

Stereoselective Synthesis of α,α‐Chlorofluoro Carbonyl Compounds Leading to the Construction of Fluorinated Chiral Quaternary Carbon Centers

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