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霍志保(Huo Zhibao) 特別研究員 性別:男 電子郵件:hzb410@sjtu.edu.cn 辦公室電話:021-54742251 傳真： |
- 納米介孔催化劑的制備及在資源循環(huán)利用中的應(yīng)用；
- 二氧化碳催化轉(zhuǎn)化及資源化；
- 綠色化學(xué)；
- 生物質(zhì)資源化利用。
- 2011 上海交通大學(xué)環(huán)境學(xué)院，特別研究員，博士生導(dǎo)師，上海市高校”東方學(xué)者”特聘教授
- 2007 日本東北大學(xué) 產(chǎn)學(xué)官連攜研究員
- 2007 日本東北大學(xué) 博士
- 2004 日本東北大學(xué) 碩士
- 近3年部分論文如下：
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1. ACS Books Book: “Advances in CO2 Conversion and Utilization” Title: “Hydrothermal conversion of CO2 into value-added products – A potential technology for improving global carbon cycle”2010, Chapter 4, 31-53.
2. Improvement of lactic acid production from cellulose with the addition of Zn/Ni/C under alkaline hydrothermal conditions. Bioresource Technology, 2010, 102, 1998-2003.
3. A Method for the Synthesis of Substituted Quinolines via Electrophilic Cyclization of 1-azido-2-(2-propynyl)-benzene. J. Org. Chem. 2010, 75, 1266-1270. 【亮點(diǎn)文章Highlight by SYNFACTS, 2010, 6, 641-641】.
4. The direct formation of 2-cyano-4-amidopyridine via α–cyanation of 4-amidopyridine N-oxide, dimethylcarbamoyl chloride and cheap potassium cyanide. Acta Chim. Slov. 2009, 56. 659-663. (被邀請(qǐng)的論文).
5. Gold-catalyzed synthesis of isoquinolines via intramolecular cyclization of 2-alkynyl benzyl azides. Tetrahedron Lett. 2009, 50, 3651-3653.
6. Iodine Mediated Electrophilic Cyclization of 2-Alkynyl-1-methylen-azide Aromatics Leading to Highly Substituted Isoquinolines and its Application to the Synthesis of Norchelerythrine. J. Am. Chem. Soc. 2008, 130, 15720-15725.
7. Iodine-mediated electrophilic cyclization of 2-alkynylbenzaldoximes leading to the formation of iodoisoquinoline N-oxides. Tetrahedron Lett. 2008, 49, 5531-5533.
8. Zinc cyanide mediated direct α-cyanation of isonicotinic acid N-oxide. Application to the synthesis of FYX-051, a xanthine oxidoreductase inhibitor.Tetrahedron Lett. 2008, 49, 4369-4371.
9. Suppresses of β-hydride elimination in the intramolecular hydrocarboxylation of alkynes leading to the formation of lactones. Adv. Synth. Catal. 2007, 349, 680-684.
10.Palladium-catalyzed three component coupling between Chromones, alcohols and Allylic Acetates: diversity oriented synthesis of highly substituted chromones. Tetrahedron. 2007, 63, 5954-5961.
