1.主要文章：

[1] Xu, Z.; Wang, X.-G.; Wei, Y.-H.; Ji, K.-L.;Zheng, J.-F.;* Ye, J.-L.; Huang, P.-Q.* Organocatalytic, Enantioselective Reductive Bis-functionalization of Secondary Amides: One-Pot Construction of Chiral 2,2-Disubstituted 3-Iminoindoline Org. Lett.2019, 21, 7587–7591.

[2] Hu, X.-N.; Xu, Z.; Cai, D.-C.; Shen, T.-L.;Zheng, J.-F.;* Huang, P.-Q.* Iridium-Catalysed Reductive Coupling Reaction of Tertiary Lactams/Amides with Isocyanoacetates Org. Chem. Front.2018, 5, 2051–2056.

[3]Zheng, J.-F.; Hu, X.-N.; Xu, Z.; Cai, D.-C.; Shen, T.-L.; Huang, P.-Q. Substrate-Controlled Chemoselective Reactions of Isocyanoacetates with Amides and Lactams J. Org. Chem.2017, 82, 9693−9703.

[4]Zheng, J.-F.;* Qian, X.-Y.; Huang, P.-Q. Direct transformation of amides: a one-pot reductive Ugi-type three-component reaction of secondary amides Org. Chem. Front.2015, 2, 927.

[5]Zheng, J.-F.;* Xie, Z.-Q.; Chen, X.-J.; Huang, P.-Q. Direct Transformation of Amides: Reductive Cycloaddition of Secondary Amides with Danishefsky Diene Acta Chim. Sinica2015, 73, 705.

[6]Zheng, J.-F.; Lan, H.-Q.; Yang, R.-F.; Peng, Q.-L.; Xiao, Z,-H.; Tuo, S.-C.; Hu, K.-Z.; Xiang, Y.-G.; Wei, Z.; Zhang, Z.; Huang P.-Q.* Asymmetric Synthesis of the Sex Pheromones and Stereoisomers of Pine Sawflies Helv. Chim. Acta2012, 95, 1799-1808.

[7] Yang, J.-F.; Liu,S.-J.;Zheng, J.-F.(共同第一作者）; (Steve) Zhou, J.-R.；Room-Temperature Suzuki–Miyaura Coupling of Heteroaryl Chlorides and Tosylates Euro. J. Org. Chem.2012, 6248-6259.

[8] Wang, Zhigang;Zheng, J.-F.*; Huang, H.-Y.; Huang, P.-Q. Asymmetric Synthesis of Both Enantiomers of Disparlure Chin. J. Chem.2012, 30, 23－28.

[9] Teng, B;Zheng, J.-F.*; Huang, H.-Y.; Huang, P.-Q.* Enantioselective Synthesis of Glutarimide Alkaloids Cordiarimides A, B, Crotonimides A, B, and Julocrotine Chin. J. Chem.2011, 29, 1312－1318.

[10] Du, Y,Zheng, J.-F., Wang, Z.-G.; Jiang, L.-J.; Ruan, Y.-P.; and Huang P.-Q* A Concise, Protection-Free and Divergent Approach for the Enantioselective Syntheses of Two Pheromonal Epoxide Components of the Fall Webworm Moth and Other Species J. Org. Chem.2010, 75, 4619－4622.

[11] Jiang, L.-J.; Lan, H.-Q.;Zheng, J.-F.*; Ye, J.-L.; Huang P.-Q* A Flexible Approach to Methyl (5S)-Alkyltetramate Derivatives Synlett2009, 297－301.

[12] Wei, Z.; Lan, H.-Q.;Zheng, J.-F.*; Huang P.-Q*. New and Concise Approach to (R)-Lipoic Acid Synth. Comm.2009, 39, 691－701.

[13]Zheng,J.-F.; Chen, W.; Huang, S.-Y.; Ye, J.-L.; Huang P.-Q*. A divergent asymmetric approach to aza-spiropyran derivative and (1S,8aR)-1-hydroxy -indolizidine Beilstein J. Org. Chem.2007, 3, 41. (highly accessed) DOI: 10.1186/1860-5397-3-41

[14]Zheng,J.-F.Jin, L.-R. Huang, P.-Q.^*_,Enantio-divergent Synthesis of Both Enantiomers of Cytoxic Marine Alkaloid Haliclorensin and Isohaliclorensin, A Constituent of Halitulin Org. Lett.2004, 6, 1139－1142.

2.专利申请12篇（已授权11篇）：

[1]一种合成S-(3)-羟基四氢呋喃的方法,郑剑峰，苏贞夏，靳立人,申请号：2006100365928,授权公告号：CN100441573C,授权公告日：2008.12.10；

[2]一种合成抗艾滋病药物安普那韦中间体的方法,郑剑峰，石国宗，苏贞夏,靳立人，申请号：2007100087679，公开号：CN101037403；

[3]一种合成碳青霉烯类抗生素药物中间体的方法，郑剑峰，陈晓飞，申请号：2007100097454，授权公告号：CN101157647B，授权公告日：2010.08.25；

[4]利托那韦水溶性衍生物及其合成方法和应用，郑剑峰，石国宗，申请号：2008100724864，授权公告号：CN101440091B，授权公告日：2012.01.04；

[5]美国白蛾性信息素的合成方法，黄培强，杜宇，郑剑峰，王志刚，申请号：2009101117914。授权公告号：CN101550117B，授权公告日：2011.03.30；

[6]美国白蛾性信息素的简便立体选择性合成方法，黄培强，杜宇，郑剑峰，申请号：2010101270211，授权公告号：CN101798293B，授权公告日：2012.05.23；

[7]一种高对映体纯松叶蜂性信息素与立体异构体的合成方法，黄培强，郑剑峰，彭启龙，张真，蓝洪桥，肖振华，杨瑞峰，庹世川，胡孔珍，项勇刚，危祯，申请号：2011100675450，授权公告号：CN102167666B，授权公告日：2013.09.18；

[8]降血糖药物分子TAPA的合成方法，黄培强，郑剑峰，王志刚，张洪奎，申请号：2011102374725，授权公告号：CN102351702B，授权公告日：2014.08.13；

[9]一种舞毒蛾性信息素的合成方法，黄培强，王志刚，郑剑峰，申请号201110149930X，公开号：CN102321050A，授权公告号：CN102321050B，授权公告日：2014.08.13；

[10]一种茶尺蠖性信息素的立体选择性合成方法，郑剑峰，梁攀，黄培强，申请号：2012104320584，公开号：CN102911136A，授权公告号：CN102911136B，授权公告日：2014.11.05；

[11]一种喹诺里西啶酮化合物的合成方法，郑剑峰，谢志强，黄培强，申请号：2015100380683，授权公告号：CN104530041B，授权公告日：2016.04.13；

[12]一种合成α,β不饱和酰胺化合物的方法，黄培强，郑剑峰，胡秀宁，蔡东城，申泰龙，授权公告号：CN106748949B，授权公告日：2019.04.09.