P. Xie*, Z. Sun, S. Li, X. Cai, J. Qiu, W. Fu, C. Gao, S. Wu, X. Yang, T.-P. Loh*, Reciprocal-activation strategy for allylic sulfination with unactivated allylic alcohols, Org. Lett. 2020,22, 4893.
P. Xie*, Z. Sun, S. Li, L. Zhang, X. Cai, W. Fu, X. Yang, Y. Liu, X. Wo, T.-P. Loh*, Dehydrative cross-coupling of allylic alcohols with alkynes, Org. Lett. 2020,22, 1599.
P. Xie*, S. Li, Y. Liu, X. Cai, J. Wang, X. Yang, T.-P. Loh*, Alkaline-earth metal-catalyzed dehydrative allylic alkylation. Org. Lett. 2020,22, 31.
P. Xie*, X. Wo, X. Yang, X. Cai, S. Li, C. Gao, W. Fu, Z. Sun, T.-P. Loh*, Calcium-catalyzed regioselective dehydrative cross-coupling of propargylic alcohols with 1,3-dicarbonyl compounds, Green Chem.2019, 21, 5207.
P. Xie*, W. Fu, X. Cai, Z. Sun, Y. Wu, S. Li, C. Gao, X. Yang, T.-P. Loh*, A Ba/Pd catalytic system enables dehydrative cross-coupling and excellent E-selective wittig reactions, Org. Lett. 2019, 21, 7055.
P. Xie*, W. Fu, Y. Wu, X. Cai, Z. Sun, S. Li, C. Gao, X. Yang, T.-P. Loh*, Allylic phosphorus ylides directly generated from alcohols with water as the only byproduct, Org. Lett. 2019, 21, 4168.
P. Xie*, J. Wang, Y. Liu, J. Fan, X. Wo, W. Fu, Z. Sun, T.-P. Loh*, Water-promoted C-S bond formation reactions, Nat. Commun.2018, 9, 1321. (Highlighted by K. J. Geogheghan, Nat. Rev. Chem. 2018, 2, 3).
Y. Liu, P. Xie*, Z. Sun, X. Wo, C. Gao, W. Fu, T.-P. Loh*, Direct substitution of secondary and tertiary alcohols to generate sulfones under catalyst and additive-free conditions, Org. Lett. 2018, 20, 5353.
P. Xie*, J. Fan, Y. Liu, X. Wo, W. Fu, T.-P. Loh*, Bronsted acid/organic photoredox cooperative catalysis: Easy access to tri- and tetra-substituted alkenylphosphorus compounds from alcohols and P-H species, Org. Lett. 2018, 20, 3341.
X. Wo, P. Xie*, W. Fu, C. Gao, Y. Liu, Z. Sun, T.-P. Loh*, Barium-catalyzed C-OH/P-H dehydrative cross-coupling for C-P Bond construction, Chem. Commun.2018, 54, 11132.
P. Xie*, J. Wang, J. Fan, Y. Liu, X. Wo, W. Fu, T.-P. Loh*, The C–OH/P–H dehydrative cross-coupling for the construction of the P–C bond under metalfree conditions, Green Chem.2017, 19, 2135.
P. Xie*, L. Guo, L. Xu, T.-P. Loh*, Asymmetric P-C bond formation:diastereoselective synthesis of adjacent P,C-stereogenic allylic phosphorus compounds, Chem. Asian J.2016, 11, 1353.
P. Xie, Y. Huang*, Morita-Baylis-Hillman adduct derivates (MBHADs): the versatile reactivity in Lewis base-promoted annulation, Org. Biomol. Chem. 2015, 13, 8578. (Review, ESI Highly Cited Paper)
Y. Yamashita, Y. Cui, P. Xie, S. Kobayashi, Zinc Amide Catalyzed Regioselective Allenylation and Propargylation of Ketones with Allenyl Boronate, Org. Lett. 2015, 17, 6042,
P. Xie, E. Li, J. Zheng, Y. Huang*, Sequential Catalyst Phosphine/Secondary Amine Promoted [1+4]/Rearrangement Domino Reaction for the Construction of (2H)-Pyrans and 2-Oxabicyclo[2.2.2]oct-5-ene Skeletons, Eur. J. Org. Chem.2014, 1189.
L. Liang, E. Li, P. Xie, Y. Huang,* Phosphine-Initiated Domino Reaction: A Convenient Method for the Preparation of Spirocyclopentanones, Chem. Asian J.2014, 9, 1270.
P. Xie, Y. Huang,* Cross-Rauhut-Currier Reactions Initiated Domino Annulations, Eur. J. Org. Chem. 2013, 6213. (Review, Invited by Editor)
P. Xie, E. Li, J. Zheng, Y. Huang,* R. Chen, Tunable Phosphine-Mediated Domino Reaction: Selective Synthesis of 2,3-Dihydrofurans and Biaryls, Adv. Synth. Catal. 2013, 355, 161. (Hot Paper, Selected by Editor).
E. Li, Y. Huang*, L. Liang, P. Xie, Phosphine-Catalyzed [4 + 2] Annulation of γ-Substituent Allenoates: Facile Access to Functionalized Spirocyclic Skeletons, Org. Lett. 2013, 15, 3138.
E. Li, P. Xie, L. Yang, L. Liang, Y. Huang,* Tuning Catalysts to Tune the Products: Phosphine-Catalyzed Aza-Michael Addition Reaction of Hydrazones with Allenoates, Chem. Asian J.2013, 8, 603.
P. Xie, Y. Huang,* R. Chen, Phosphine-Mediated Domino Benzannulation Strategy for the Construction of Highly Functionalized Multiaryl Skeletons, Chem. Eur. J. 2012,18, 7362. (Most Accessed in May 2012, Top 10)
P. Xie, W. Lai, Z. Geng, Y. Huang,* R. Chen, Phosphine-Catalyzed Domino Reaction for the Synthesis of Conjugated 2,3- Dihydrofurans from Allenoates and Nazarov Reagents, Chem. Asian J. 2012, 7, 1533.
L. Yang, P. Xie, E. Li, X. Li, Y. Huang,* R. Chen, Phosphine-catalyzed domino reaction: an efficient method for the synthesis of highly functionalized spiro[furan-indoline]diones, Org. Biomol. Chem.2012, 10, 7628.
X. Meng, P. Xie, Y. Huang,* R. Chen, Organocatalytic domino reaction of salicyl N-thiophosphoryl imines and methyl vinyl ketone initiated by an aza-MBH reaction with bifunctional phosphine catalysts, RSC Adv. 2012, 2, 8104.
P. Xie#, L. Wang#, L. Yang, E. Li, J. Ma, Y. Huang,* R. Chen, Domino Reaction for the Chemo- and Stereoselective Synthesis of trans-2,3-Dihydrobenzofurans from N-Thiophosphinyl Imines and Sulfur Ylides, J. Org. Chem.2011,76, 7699. (#Equal contribution)
P. Xie, Y. Huang,* W. Lai, X. Meng, Ruyu Chen, Bifunctional Phosphine -catalyzed cross-Rauhut–Currier/Michael/AldolCondensation Triple Domino Reaction: Synthesis of Functionalized Cyclohexenes, Org. Biomol. Chem.2011, 9, 6707.
J. Ma, P. Xie, C. Hu, Y. Huang,* R. Chen, Substrate-Controlled, Phosphine-Catalyzed Domino Reactions of Activated Conjugated Dienes: Highly Diastereoselective Synthesis of Bicyclic Skeletons, Chem. Eur. J. 2011,17, 7418.
P. Xie, Y. Huang,* R. Chen,* Phosphine-Catalyzed Domino Reaction: Highly Stereoselective Synthesis of trans-2,3-Dihydrobenzofurans from Salicyl N-Thiophosphinyl Imines and Allylic Carbonates, Org. Lett. 2010, 12, 3768-3771.
X. Meng, Y. Huang*, H. Zhao, P. Xie, J. Ma, R. Chen, PPh3-Catalyzed Domino Reaction: A Facile Method for the Synthesis of Chroman Derivatives, Org. Lett. 2009, 11, 991.