| Year |
Citation |
Score |
| 2024 |
Xu FF, Chen JQ, Shao DY, Huang PQ. Author Correction: Catalytic enantioselective reductive alkynylation of amides enables one-pot syntheses of pyrrolidine, piperidine and indolizidine alkaloids. Nature Communications. 15: 1836. PMID 38418446 DOI: 10.1038/s41467-024-46252-5 |
0.308 |
|
| 2023 |
Xu FF, Chen JQ, Shao DY, Huang PQ. Catalytic enantioselective reductive alkynylation of amides enables one-pot syntheses of pyrrolidine, piperidine and indolizidine alkaloids. Nature Communications. 14: 6251. PMID 37803030 DOI: 10.1038/s41467-023-41846-x |
0.38 |
|
| 2023 |
Ji KL, He SF, Xu DD, He WX, Zheng JF, Huang PQ. Concise Total Synthesis of (-)-Quinocarcin Enabled by Catalytic Enantioselective Reductive 1,3-Dipolar Cycloaddition of Secondary Amides. Angewandte Chemie (International Ed. in English). e202302832. PMID 37025034 DOI: 10.1002/anie.202302832 |
0.39 |
|
| 2022 |
Chen H, Wu ZZ, Shao DY, Huang PQ. Multicatalysis protocol enables direct and versatile enantioselective reductive transformations of secondary amides. Science Advances. 8: eade3431. PMID 36417504 DOI: 10.1126/sciadv.ade3431 |
0.337 |
|
| 2022 |
Wu DP, Ou W, Huang PQ. Ir-Catalyzed Chemoselective Reductive Condensation Reactions of Tertiary Amides with Active Methylene Compounds. Organic Letters. 24: 5366-5371. PMID 35849542 DOI: 10.1021/acs.orglett.2c02045 |
0.316 |
|
| 2022 |
Hong YC, Ye JL, Huang PQ. One-Pot Synthesis of α-Amino Bisphosphonates from Nitriles via TfO/HC(OR)-Mediated Interrupted Ritter-Type Reaction. The Journal of Organic Chemistry. PMID 35748643 DOI: 10.1021/acs.joc.2c00718 |
0.347 |
|
| 2021 |
He Q, Ye JL, Xu FF, Geng H, Chen TT, Chen H, Huang PQ. TfO/TTBP (2,4,6-Tri--butylpyrimidine): An Alternative Amide Activation System for the Direct Transformations of Both Tertiary and Secondary Amides. The Journal of Organic Chemistry. PMID 34499513 DOI: 10.1021/acs.joc.1c01572 |
0.311 |
|
| 2021 |
Lin Y, He SF, Geng H, Xiao YC, Ji KL, Zheng JF, Huang PQ. Chemoselective Reactions of Isocyanates with Secondary Amides: One-Pot Construction of 2,3-Dialkyl-Substituted Quinazolinones. The Journal of Organic Chemistry. PMID 33710879 DOI: 10.1021/acs.joc.0c02929 |
0.321 |
|
| 2021 |
Huang YQ, Huang XZ, Huang PQ. Synthesis of 5-(1-Alkoxyalkylidene)tetronates by Direct Condensation Reactions of Tetronates with Thionolactones and Thionoesters. The Journal of Organic Chemistry. PMID 33491453 DOI: 10.1021/acs.joc.0c02502 |
0.351 |
|
| 2021 |
Chen DH, Sun WT, Zhu CJ, Lu GS, Wu DP, Wang AE, Huang PQ. Enantioselective Reductive Cyanation and Phosphonylation of Secondary Amides by Ir and Chiral Thiourea Sequential Catalysis. Angewandte Chemie (International Ed. in English). PMID 33484032 DOI: 10.1002/anie.202015898 |
0.331 |
|
| 2021 |
Huang SY, Gao LH, Huang XZ, Huang PQ. Enantioselective Total Syntheses of the Proposed and Revised Structures of Methoxystemofoline: A Stereochemical Revision. The Journal of Organic Chemistry. PMID 33440938 DOI: 10.1021/acs.joc.0c02667 |
0.361 |
|
| 2020 |
Huang XZ, Gao LH, Huang PQ. Enantioselective total syntheses of (+)-stemofoline and three congeners based on a biogenetic hypothesis. Nature Communications. 11: 5314. PMID 33082332 DOI: 10.1038/s41467-020-19163-4 |
0.31 |
|
| 2020 |
Hu XN, Wu DP, Xu YP, Huang PQ. Organocatalytic Asymmetric Synthesis of an Advanced Intermediate of (+)-Sarain A. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33044771 DOI: 10.1002/chem.202004261 |
0.357 |
|
| 2020 |
Huang P. Procedure-Economical, Enantioselective Total Syntheses of Polycyclic Natural Products and Analogues Containing a 3a-Hydroxyhexahydropyrrolo[2,3-b]indole-2-carboxylic Acid Residue Synlett. DOI: 10.1055/S-0040-1707164 |
0.409 |
|
| 2020 |
Wu J, Huang P. Concise, enantioselective total syntheses of both the proposed and revised structures of (−)-versiquinazoline H Chinese Chemical Letters. 31: 61-63. DOI: 10.1016/J.Cclet.2019.06.043 |
0.444 |
|
| 2020 |
Chen H, Chen D, Huang P. Ni-catalyzed direct alcoholysis of N -acylpyrrole-type tertiary amides under mild conditions Science China-Chemistry. 63: 370-376. DOI: 10.1007/S11426-019-9665-5 |
0.384 |
|
| 2020 |
Ou W, Huang P. Amides as surrogates of aldehydes for C-C bond formation: amide-based direct Knoevenagel-type condensation reaction and related reactions Science China-Chemistry. 63: 11-15. DOI: 10.1007/S11426-019-9586-3 |
0.402 |
|
| 2020 |
Luo S, Huang X, Guo L, Huang P. Catalytic Asymmetric Total Synthesis of Macrocyclic Marine Natural Product (‐)‐Haliclonin A Chinese Journal of Chemistry. DOI: 10.1002/Cjoc.202000291 |
0.387 |
|
| 2019 |
Xu Z, Wang XG, Wei YH, Ji KL, Zheng JF, Ye JL, Huang PQ. Organocatalytic, Enantioselective Reductive Bis-functionalization of Secondary Amides: One-Pot Construction of Chiral 2,2-Disubstituted 3-Iminoindoline. Organic Letters. PMID 31479277 DOI: 10.1021/Acs.Orglett.9B02862 |
0.446 |
|
| 2019 |
Chen H, Huang YH, Ye JL, Huang PQ. Double Addition of Alkynyllithium Reagents to Amides/Lactams: A Direct and Flexible Synthesis of 3-Amino-1,4-diynes Bearing an Aza-Quaternary Carbon Center. The Journal of Organic Chemistry. PMID 31287315 DOI: 10.1021/Acs.Joc.9B01416 |
0.438 |
|
| 2019 |
Chen TT, Wang AE, Huang PQ. Chemoselective Synthesis of α-Amino-α-cyanophosphonates by Reductive Gem-Cyanation-Phosphonylation of Secondary Amides. Organic Letters. PMID 31059269 DOI: 10.1021/Acs.Orglett.9B01257 |
0.41 |
|
| 2019 |
Liu ZJ, Huang PQ. Biomimetic Enantioselective Total Synthesis of (-)-Robustanoids A, B and Analogs. The Journal of Organic Chemistry. PMID 30957497 DOI: 10.1021/Acs.Joc.9B00573 |
0.463 |
|
| 2019 |
Huang YH, Wang SR, Wu DP, Huang PQ. Intermolecular Dehydrative [4 + 2] Aza-Annulation of N-Arylamides with Alkenes: A Direct and Divergent Entrance to Aza-Heterocycles. Organic Letters. PMID 30807190 DOI: 10.1021/Acs.Orglett.9B00233 |
0.378 |
|
| 2019 |
Liu Y, Zheng X, Huang P. Photoredox Catalysis for the Coupling Reaction of Nitrones with Aromatic Tertiary Amines Acta Chimica Sinica. 77: 850. DOI: 10.6023/A19040150 |
0.373 |
|
| 2019 |
Yang Z, Lu G, Ye J, Huang P. Ir-catalyzed chemoselective reduction of β-amido esters: A versatile approach to β-enamino esters Tetrahedron. 75: 1624-1631. DOI: 10.1016/J.Tet.2018.12.024 |
0.331 |
|
| 2019 |
Cheng J, Zheng X, Huang P. Construction of multifunctional heterocycles bearing aza-quaternary carbons by titanocene-catalyzed umpolung reactions Tetrahedron. 75: 1612-1623. DOI: 10.1016/J.Tet.2018.11.067 |
0.371 |
|
| 2019 |
Liu Y, Zhu C, Yu C, Wang A, Huang P. Tf2O‐Mediated Intermolecular Coupling of Secondary Amides with Enamines or Ketones: A Versatile and Direct Access to β‐Enaminones European Journal of Organic Chemistry. 2019: 7169-7174. DOI: 10.1002/Ejoc.201901354 |
0.353 |
|
| 2019 |
Wu D, He Q, Chen D, Ye J, Huang P. Cover Picture: A Stepwise Annulation for the Transformation of Cyclic Ketones to Fused 6 and 7‐Membered Cyclic Enimines and Enones (Chin. J. Chem. 4/2019) Chinese Journal of Chemistry. 37: 305-305. DOI: 10.1002/Cjoc.201990041 |
0.326 |
|
| 2019 |
Geng H, Huang P. Ketone Synthesis by Direct, Orthogonal Chemoselective Hydroacylation of Alkenes with Amides: Use of Alkenes as Surrogates of Alkyl Carbanions Chinese Journal of Chemistry. 37: 811-816. DOI: 10.1002/Cjoc.201900252 |
0.466 |
|
| 2019 |
Wang S, Huang P. Cross‐Coupling of Secondary Amides with Tertiary Amides: The Use of Tertiary Amides as Surrogates of Alkyl Carbanions for Ketone Synthesis Chinese Journal of Chemistry. 37: 887-891. DOI: 10.1002/Cjoc.201900215 |
0.448 |
|
| 2019 |
Wu D, He Q, Chen D, Ye J, Huang P. A Stepwise Annulation for the Transformation of Cyclic Ketones to Fused 6 and 7‐Membered Cyclic Enimines and Enones Chinese Journal of Chemistry. 37: 315-322. DOI: 10.1002/Cjoc.201900035 |
0.325 |
|
| 2019 |
Liu Y, Wang S, Chen T, Yu C, Wang A, Huang P. Enamines as Surrogates of Alkyl Carbanions for the Direct Conversion of Secondary Amides to α-Branched Ketones Advanced Synthesis & Catalysis. 361: 971-975. DOI: 10.1002/Adsc.201801443 |
0.37 |
|
| 2018 |
Geng H, Huang PQ. Rapid Generation of Molecular Complexity by Chemical Synthesis: Highly Efficient Total Synthesis of Hexacyclic Alkaloid (-)-Chaetominine and Its Biosynthetic Implications. Chemical Record (New York, N.Y.). PMID 30252197 DOI: 10.1002/tcr.201800079 |
0.313 |
|
| 2018 |
Ou W, Han F, Hu XN, Chen H, Huang PQ. Iridium-Catalyzed Reductive Alkylations of Secondary Amides. Angewandte Chemie (International Ed. in English). PMID 29979492 DOI: 10.1002/Anie.201806747 |
0.42 |
|
| 2018 |
Yang ZP, He Q, Ye JL, Huang PQ. Asymmetric Total Synthesis and Absolute Configuration Determination of (-)-Verrupyrroloindoline. Organic Letters. PMID 29969900 DOI: 10.1021/Acs.Orglett.8B01579 |
0.455 |
|
| 2018 |
Fan T, Wang A, Li JQ, Ye JL, Zheng X, Huang PQ. A Versatile One-Pot Synthesis of Polysubstituted Cyclopent-2-enimines from α,β-Unsaturated Amides via Imino-Nazarov Reaction. Angewandte Chemie (International Ed. in English). PMID 29924902 DOI: 10.1002/Anie.201805641 |
0.44 |
|
| 2018 |
Liu Y, Mao Z, Pradal A, Huang PQ, Oble J, Poli G. Palladium-Catalyzed [3 + 2]-C-C/N-C Bond-Forming Annulation. Organic Letters. PMID 29897775 DOI: 10.1021/Acs.Orglett.8B01616 |
0.431 |
|
| 2018 |
Wang AE, Yu CC, Chen TT, Liu YP, Huang PQ. Enamines as Surrogates of Alkene Carbanions for the Reductive Alkenylation of Secondary Amides: An Approach to Allylamines. Organic Letters. PMID 29384685 DOI: 10.1021/Acs.Orglett.7B03943 |
0.418 |
|
| 2018 |
Ye CX, Melcamu YY, Li HH, Cheng JT, Zhang TT, Ruan YP, Zheng X, Lu X, Huang PQ. Dual catalysis for enantioselective convergent synthesis of enantiopure vicinal amino alcohols. Nature Communications. 9: 410. PMID 29379007 DOI: 10.1038/S41467-017-02698-4 |
0.426 |
|
| 2018 |
Hu X, Shen T, Cai D, Zheng J, Huang P. The iridium-catalysed reductive coupling reaction of tertiary lactams/amides with isocyanoacetates Organic Chemistry Frontiers. 5: 2051-2056. DOI: 10.1039/C8Qo00312B |
0.465 |
|
| 2018 |
Chen H, Ye J, Huang P. Chemoselective direct reductive trifluoromethylation of amides: a flexible access to functionalized α-trifluoromethylamines Organic Chemistry Frontiers. 5: 943-947. DOI: 10.1039/C7Qo01031A |
0.343 |
|
| 2018 |
Huang P, Geng H. Ni-Catalyzed chemoselective alcoholysis of N-acyloxazolidinones Green Chemistry. 20: 593-599. DOI: 10.1039/C7Gc03534A |
0.425 |
|
| 2018 |
Ye J, Zhu Y, Geng H, Huang P. Metal-free synthesis of quinolines by direct condensation of amides with alkynes: revelation of N -aryl nitrilium intermediates by 2D NMR techniques Science China-Chemistry. 61: 687-694. DOI: 10.1007/S11426-017-9160-1 |
0.402 |
|
| 2017 |
Huang PQ, Chen H. Ni-Catalyzed cross-coupling reactions of N-acylpyrrole-type amides with organoboron reagents. Chemical Communications (Cambridge, England). PMID 29124262 DOI: 10.1039/C7Cc07457C |
0.433 |
|
| 2017 |
Zheng JF, Hu XN, Xu Z, Cai DC, Shen TL, Huang PQ. Substrate-Controlled Chemoselective Reactions of Isocyanoacetates with Amides and Lactams. The Journal of Organic Chemistry. PMID 28850230 DOI: 10.1021/Acs.Joc.7B01768 |
0.425 |
|
| 2017 |
Huang P, Huang Y, Wang S. One-pot synthesis of N-heterocycles and enimino carbocycles by tandem dehydrative coupling–reductive cyclization of halo-sec-amides and dehydrative cyclization of olefinic sec-amides Organic Chemistry Frontiers. 4: 431-444. DOI: 10.1039/C6Qo00720A |
0.511 |
|
| 2017 |
Mao Z, Martini E, Prestat G, Oble J, Huang P, Poli G. Analogues of the 2-carboxyl-6-hydroxyoctahydroindole (CHOI) unit from diverging Pd-catalyzed allylations: Selectivity as a function of the double bond position Tetrahedron Letters. 58: 4174-4178. DOI: 10.1016/J.Tetlet.2017.09.046 |
0.338 |
|
| 2017 |
Gao Y, Luo S, Ye J, Huang P. An attempted approach to the tricyclic core of haliclonin A: Structural elucidation of the final product by 2D NMR Chinese Chemical Letters. 28: 1176-1181. DOI: 10.1016/J.Cclet.2017.04.016 |
0.366 |
|
| 2017 |
Huang P, Fan T. Intramolecular Keto Lactam Condensation: A Convenient and Straightforward Approach to Bicyclic Vinylogous Lactams European Journal of Organic Chemistry. 2017: 6369-6374. DOI: 10.1002/Ejoc.201701060 |
0.474 |
|
| 2017 |
Huang P, Ou W. A Direct, Versatile, and Chemoselective Synthesis of Vinylogous Bis‐ and Monourethanes/amides and β‐Keto Esters by Aza‐Knoevenagel‐Type Reactions of Tertiary Amides with Enolates European Journal of Organic Chemistry. 2017: 582-592. DOI: 10.1002/Ejoc.201601326 |
0.488 |
|
| 2017 |
Huang P, Huang Y. Further Studies on the Direct Synthesis of α,β‐Unsaturated Ketimines and α,β‐Enones by Chemoselective Dehydrative Addition of Functionalized Alkenes to Secondary Amides Chinese Journal of Chemistry. 35: 613-620. DOI: 10.1002/Cjoc.201600700 |
0.377 |
|
| 2016 |
Huang PQ, Ou W, Han F. Chemoselective reductive alkynylation of tertiary amides by Ir and Cu(i) bis-metal sequential catalysis. Chemical Communications (Cambridge, England). 52: 11967-11970. PMID 27722243 DOI: 10.1039/C6Cc05318A |
0.378 |
|
| 2016 |
Huang PQ, Huang YH, Xiao KJ. Metal-free Intermolecular Coupling of Arenes with Secondary Amides: Chemoselective Synthesis of Aromatic Ketimines and Ketones, and N-Deacylation of Secondary Amides. The Journal of Organic Chemistry. PMID 27603045 DOI: 10.1021/Acs.Joc.6B01647 |
0.441 |
|
| 2016 |
Huang PQ, Huang YH, Geng H, Ye JL. Metal-Free C-H Alkyliminylation and Acylation of Alkenes with Secondary Amides. Scientific Reports. 6: 28801. PMID 27356173 DOI: 10.1038/Srep28801 |
0.422 |
|
| 2016 |
Huang PQ, Lang QW, Hu XN. One-pot Reductive 1,3-Dipolar Cycloaddition of Secondary Amides: A Two-Step Transformation of Primary Amides. The Journal of Organic Chemistry. PMID 27285664 DOI: 10.1021/Acs.Joc.6B01080 |
0.455 |
|
| 2016 |
Huang PQ, Lang QW, Wang YR. Mild Metal-free Hydrosilylation of Secondary Amides to Amines. The Journal of Organic Chemistry. PMID 27100232 DOI: 10.1021/Acs.Joc.6B00572 |
0.459 |
|
| 2016 |
Huang PQ, Huang SY, Gao LH, Mao ZY, Chang Z, Wang AE. Correction: Enantioselective total synthesis of (+)-methoxystemofoline and (+)-isomethoxystemofoline. Chemical Communications (Cambridge, England). PMID 26963893 DOI: 10.1039/C6Cc90127A |
0.304 |
|
| 2016 |
Guo LD, Huang XZ, Luo SP, Cao WS, Ruan YP, Ye JL, Huang PQ. Organocatalytic, Asymmetric Total Synthesis of (-)-Haliclonin A. Angewandte Chemie (International Ed. in English). PMID 26890255 DOI: 10.1002/Anie.201512005 |
0.468 |
|
| 2016 |
Huang P, Mao Z, Geng H. Enantioselective total synthesis and structural revision of (-)-isochaetominine Chinese Journal of Organic Chemistry. 36: 315-324. DOI: 10.6023/Cjoc201512015 |
0.414 |
|
| 2016 |
Ye JL, Liu Y, Zhang YF, Yang ZP, Huang PQ. Studies on the Second-Generation Approach to Loline Alkaloids: Synthesis of N -Bus-norloline through N - Tert -Butanesulfinyl Imine Based Asymmetric Vinylogous Mannich Reaction Synthesis (Germany). 48: 1684-1692. DOI: 10.1055/S-0035-1561432 |
0.468 |
|
| 2016 |
Ye J, Chen H, Zhang Y, Huang P. A versatile access to vicinal diamine motifs by highly anti-selective asymmetric vinylogous Mannich reactions: an efficient total synthesis of (+)-absouline Organic Chemistry Frontiers. 3: 683-692. DOI: 10.1039/C6Qo00022C |
0.449 |
|
| 2016 |
Mao ZY, Geng H, Zhang TT, Ruan YP, Ye JL, Huang PQ. Stereodivergent and enantioselective total syntheses of isochaetominines A-C and four pairs of isochaetominine C enantiomers: A six-step approach Organic Chemistry Frontiers. 3: 24-37. DOI: 10.1039/C5Qo00298B |
0.355 |
|
| 2016 |
Lang Q, Hu X, Huang P. Tf2O-TMDS combination for the direct reductive transformation of secondary amides to aldimines, aldehydes, and/or amines Science China-Chemistry. 59: 1638-1644. DOI: 10.1007/S11426-016-0224-5 |
0.437 |
|
| 2015 |
Ye JL, Liu Y, Yang ZP, Huang PQ. The asymmetric total synthesis of (+)-N-acetyl norloline. Chemical Communications (Cambridge, England). PMID 26538080 DOI: 10.1039/C5Cc07480K |
0.475 |
|
| 2015 |
Zheng X, He J, Li HH, Wang A, Dai XJ, Wang AE, Huang PQ. Titanocene(III)-Catalyzed Three-Component Reaction of Secondary Amides, Aldehydes, and Electrophilic Alkenes. Angewandte Chemie (International Ed. in English). PMID 26404091 DOI: 10.1002/Anie.201506907 |
0.457 |
|
| 2015 |
Huang PQ, Huang YH, Xiao KJ, Wang Y, Xia XE. A general method for the one-pot reductive functionalization of secondary amides. The Journal of Organic Chemistry. 80: 2861-8. PMID 25654370 DOI: 10.1021/Jo502929X |
0.422 |
|
| 2015 |
Wang AE, Chang Z, Sun WT, Huang PQ. General and chemoselective bisphosphonylation of secondary and tertiary amides. Organic Letters. 17: 732-5. PMID 25625596 DOI: 10.1021/Acs.Orglett.5B00004 |
0.352 |
|
| 2015 |
Huang PQ, Huang SY, Gao LH, Mao ZY, Chang Z, Wang AE. Enantioselective total synthesis of (+)-methoxystemofoline and (+)-isomethoxystemofoline. Chemical Communications (Cambridge, England). 51: 4576-8. PMID 25607771 DOI: 10.1039/C4Cc09598G |
0.431 |
|
| 2015 |
Zheng X, Liu J, Ye CX, Wang A, Wang AE, Huang PQ. SmI2-mediated radical coupling strategy to Securinega alkaloids: total synthesis of (-)-14,15-dihydrosecurinine and formal total synthesis of (-)-securinine. The Journal of Organic Chemistry. 80: 1034-41. PMID 25496326 DOI: 10.1021/Jo502522X |
0.427 |
|
| 2015 |
Huang PQ, Lang QW, Wang AE, Zheng JF. Direct reductive coupling of secondary amides: chemoselective formation of vicinal diamines and vicinal amino alcohols. Chemical Communications (Cambridge, England). 51: 1096-9. PMID 25450880 DOI: 10.1039/C4Cc08330J |
0.392 |
|
| 2015 |
Zheng J, Xie Z, Chen X, Huang P. Direct Transformation of Amides: Reductive Cycloaddition of Secondary Amides with Danishefsky Diene Acta Chimica Sinica. 73: 705. DOI: 10.6023/A15060395 |
0.425 |
|
| 2015 |
Huang PQ, Ou W, Ye JL. Aza-Knoevenagel-type condensation of secondary amides: Direct access to N-monosubstituted β,β-difunctionalized enamines Organic Chemistry Frontiers. 2: 1094-1106. DOI: 10.1039/C5Qo00191A |
0.385 |
|
| 2015 |
Zheng J, Qian X, Huang P. Direct transformation of amides: a one-pot reductive Ugi-type three-component reaction of secondary amides Organic Chemistry Frontiers. 2: 927-935. DOI: 10.1039/C5Qo00146C |
0.388 |
|
| 2015 |
Ye J, Zhang Y, Liu Y, Zhang J, Ruan Y, Huang P. Studies on the asymmetric synthesis of pandamarilactonines: an unexpected syn-selective vinylogous Mannich reaction of N-tert-butanesulfinimines Organic Chemistry Frontiers. 2: 697-704. DOI: 10.1039/C5Qo00098J |
0.461 |
|
| 2015 |
Huang PQ, Geng H. Simple, versatile, and chemoselective reduction of secondary amides and lactams to amines with the Tf2O-NaBH4 or Cp2ZrHCl-NaBH4 system Organic Chemistry Frontiers. 2: 150-158. DOI: 10.1039/C4Qo00317A |
0.447 |
|
| 2015 |
Huang P, Wang Y, Luo S, Geng H, Ruan Y, Wang A. Procedure—economical enantioselective total syntheses of asperlicins C and E Tetrahedron Letters. 56: 1255-1258. DOI: 10.1016/J.Tetlet.2015.01.084 |
0.383 |
|
| 2015 |
Huang P, Wang Y, Xiao K, Huang Y. A general method for the direct transformation of common tertiary amides into ketones and amines by addition of Grignard reagents Tetrahedron. 71: 4248-4254. DOI: 10.1016/J.Tet.2015.04.074 |
0.418 |
|
| 2015 |
Geng H, Huang PQ. Versatile and chemoselective transformation of aliphatic and aromatic secondary amides to nitriles Tetrahedron. 71: 3795-3801. DOI: 10.1016/J.Tet.2015.03.094 |
0.417 |
|
| 2015 |
Wang A, Chang Z, Liu Y, Huang P. Mild N-deacylation of secondary amides by alkylation with organocerium reagents Chinese Chemical Letters. 26: 1055-1058. DOI: 10.1016/J.Cclet.2015.05.033 |
0.462 |
|
| 2015 |
Huang P, Geng H, Tian Y, Peng Q, Xiao K. The first enantioselective total synthesis of (+)-preussin B and an improved synthesis of (+)-preussin by step-economical methods Science China-Chemistry. 58: 478-482. DOI: 10.1007/S11426-014-5270-0 |
0.482 |
|
| 2015 |
Luo SP, Geng H, Wang Y, Huang PQ. Low-valent titanium-mediated enantioselective synthesis of quinazolinone alkaloids circumdatins F, H, and analogs Chinese Journal of Chemistry. 33: 646-654. DOI: 10.1002/Cjoc.201400849 |
0.404 |
|
| 2015 |
Huang PQ, Ou W, Ye JL. Towards reaction control: An expeditious access to racemic 5-substituted tetramates and 5-substituted tetramic acids from malimides Chinese Journal of Chemistry. 33: 655-662. DOI: 10.1002/Cjoc.201400762 |
0.421 |
|
| 2014 |
Huang PQ, Ou W, Xiao KJ, Wang AE. Tertiary amide-based Knoevenagel-type reactions: a direct, general, and chemoselective approach to enaminones. Chemical Communications (Cambridge, England). 50: 8761-3. PMID 24967872 DOI: 10.1039/C4Cc03826F |
0.396 |
|
| 2014 |
Xu CP, Luo SP, Wang AE, Huang PQ. Complexity generation by chemical synthesis: a five-step synthesis of (-)-chaetominine from L-tryptophan and its biosynthetic implications. Organic & Biomolecular Chemistry. 12: 2859-63. PMID 24675877 DOI: 10.1039/C4Ob00314D |
0.363 |
|
| 2014 |
Peng QL, Luo SP, Xia XE, Liu LX, Huang PQ. The four-step total synthesis of (-)-chaetominine. Chemical Communications (Cambridge, England). 50: 1986-8. PMID 24413776 DOI: 10.1039/C3Cc48833K |
0.454 |
|
| 2014 |
Wang A, Huang P. Efficient asymmetric syntheses of alkaloids and medicinally relevant molecules based on heterocyclic chiral building blocks Pure and Applied Chemistry. 86: 1227-1235. DOI: 10.1515/Pac-2013-1210 |
0.352 |
|
| 2014 |
Deng H, Qian X, Li Y, Zheng J, Xie L, Huang P. A versatile two-step method for the reductive alkylation and formal [4 + 2] annulation of secondary lactams: step economical syntheses of the ant venom alkaloids (2R,5S)-2-butyl-5-propylpyrrolidine and (+)-monomorine I Organic Chemistry Frontiers. 1: 258. DOI: 10.1039/C3Qo00065F |
0.488 |
|
| 2014 |
Wang X, Wang A, Huang P. A concise formal stereoselective total synthesis of (−)-swainsonine Chinese Chemical Letters. 25: 193-196. DOI: 10.1016/J.Cclet.2013.12.003 |
0.322 |
|
| 2014 |
Mao Z, Huang S, Gao L, Wang A, Huang P. A novel and versatile method for the enantioselective syntheses of tropane alkaloids Science China-Chemistry. 57: 252-264. DOI: 10.1007/S11426-013-4998-2 |
0.374 |
|
| 2014 |
Luo S, Peng Q, Xu C, Wang A, Huang P. Bio-inspired Step-Economical, Redox-Economical and Protecting-Group-Free Enantioselective Total Syntheses of (−)-Chaetominine and Analogues Chinese Journal of Chemistry. 32: 757-770. DOI: 10.1002/Cjoc.201400413 |
0.427 |
|
| 2013 |
Zhang J, Zhang HK, Huang PQ. Towards stereochemical control: A short formal enantioselective total synthesis of pumiliotoxins 251D and 237A. Beilstein Journal of Organic Chemistry. 9: 2358-66. PMID 24367400 DOI: 10.3762/Bjoc.9.271 |
0.32 |
|
| 2013 |
Wang XG, Wang AE, Hao Y, Ruan YP, Huang PQ. Modular enantioselective synthesis of 8-aza-prostaglandin E1. The Journal of Organic Chemistry. 78: 9488-93. PMID 23957245 DOI: 10.1021/Jo401412G |
0.343 |
|
| 2013 |
Xiao KJ, Luo JM, Xia XE, Wang Y, Huang PQ. General one-pot reductive gem-bis-alkylation of tertiary lactams/amides: rapid construction of 1-azaspirocycles and formal total synthesis of (±)-cephalotaxine. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 13075-86. PMID 23956001 DOI: 10.1002/Chem.201302096 |
0.343 |
|
| 2013 |
Xiao KJ, Wang Y, Huang YH, Wang XG, Huang PQ. A direct and general method for the reductive alkylation of tertiary lactams/amides: application to the step economical synthesis of alkaloid (-)-morusimic acid D. The Journal of Organic Chemistry. 78: 8305-11. PMID 23909394 DOI: 10.1021/Jo4007656 |
0.479 |
|
| 2013 |
Huang SY, Chang Z, Tuo SC, Gao LH, Wang AE, Huang PQ. Versatile construction of functionalized tropane ring systems based on lactam activation: enantioselective synthesis of (+)-pervilleine B. Chemical Communications (Cambridge, England). 49: 7088-90. PMID 23824038 DOI: 10.1039/C3Cc43665A |
0.38 |
|
| 2013 |
Zheng X, Dai XJ, Yuan HQ, Ye CX, Ma J, Huang PQ. Umpolung of hemiaminals: titanocene-catalyzed dehydroxylative radical coupling reactions with activated alkenes. Angewandte Chemie (International Ed. in English). 52: 3494-8. PMID 23420540 DOI: 10.1002/Anie.201210088 |
0.33 |
|
| 2013 |
Luo SP, Guo LD, Gao LH, Li S, Huang PQ. Toward the total synthesis of haliclonin A: construction of a tricyclic substructure. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 87-91. PMID 23225701 DOI: 10.1002/Chem.201203203 |
0.437 |
|
| 2013 |
Huo HH, Xia XE, Zhang HK, Huang PQ. Enantioselective total syntheses of (-)-FR901483 and (+)-8-epi-FR901483. The Journal of Organic Chemistry. 78: 455-65. PMID 23214918 DOI: 10.1021/Jo302362B |
0.465 |
|
| 2013 |
Liu XK, Ye JL, Ruan YP, Li YX, Huang PQ. Total synthesis of (-)-sessilifoliamide J. The Journal of Organic Chemistry. 78: 35-41. PMID 22946828 DOI: 10.1021/Jo3014484 |
0.47 |
|
| 2013 |
Hu KZ, Ma J, Qiu S, Zheng X, Huang PQ. SmI2-mediated intermolecular coupling of γ-lactam N-α-radicals with activated alkenes: asymmetric synthesis of 11-hydroxylated analogues of the lead compounds CP-734432 and PF-04475270. The Journal of Organic Chemistry. 78: 1790-801. PMID 22853560 DOI: 10.1021/Jo301277N |
0.465 |
|
| 2013 |
Zhang JL, Chen LA, Xu RB, Wang CF, Ruan YP, Wang AE, Huang PQ. Chiral imidazo[1,5-a]tetrahydroquinoline N-heterocyclic carbenes and their copper complexes for asymmetric catalysis Tetrahedron Asymmetry. 24: 492-498. DOI: 10.1016/J.Tetasy.2013.03.004 |
0.306 |
|
| 2013 |
Guo L, Liang P, Zheng J, Huang P. A Concise and Divergent Approach to Hydroxylated Piperidine Alkaloids and Azasugar Lactams European Journal of Organic Chemistry. 2013: 2230-2236. DOI: 10.1002/Ejoc.201201618 |
0.312 |
|
| 2013 |
Tuo S, Liu X, Huang P. Towards Stereochemical Control: Two Approaches for the Highly anti-Diastereoselective Construction of the Spirolactone Moieties of Some Stemona Alkaloids Chinese Journal of Chemistry. 31: 55-62. DOI: 10.1002/Cjoc.201200904 |
0.455 |
|
| 2013 |
Chen LA, Wang CF, Lin MG, Zhang JL, Huang PQ, Wang AE. Design and Synthesis of Camphor-derived Chiral [1,2,4]Triazolo[4,3-a]tetrahydroquinoline N-Heterocyclic Carbene Precursors by Pd-Catalyzed Coupling Reactions of Aryl Hydrazides with a Pyridyl Triflate Derivative Asian Journal of Organic Chemistry. 2: 294-298. DOI: 10.1002/Ajoc.201300024 |
0.377 |
|
| 2012 |
Huo HH, Zhang HK, Xia XE, Huang PQ. A formal enantioselective total synthesis of FR901483. Organic Letters. 14: 4834-7. PMID 22937903 DOI: 10.1021/Ol302165D |
0.465 |
|
| 2012 |
Xiao KJ, Wang AE, Huang PQ. Direct transformation of secondary amides into secondary amines: triflic anhydride activated reductive alkylation. Angewandte Chemie (International Ed. in English). 51: 8314-7. PMID 22807195 DOI: 10.1002/Anie.201204098 |
0.322 |
|
| 2012 |
Wang YH, Ye JL, Wang AE, Huang PQ. Reductive hydroxyalkylation/alkylation of amines with lactones/esters. Organic & Biomolecular Chemistry. 10: 6504-11. PMID 22752071 DOI: 10.1039/C2Ob25901J |
0.432 |
|
| 2012 |
Xu CP, Huang PQ, Py S. SmI2-mediated coupling of nitrones and tert-butanesulfinyl imines with allenoates: synthesis of β-methylenyl-γ-lactams and tetramic acids. Organic Letters. 14: 2034-7. PMID 22489917 DOI: 10.1021/Ol300550X |
0.373 |
|
| 2012 |
Chen GY, Huang H, Ye JL, Wang AE, Huang HY, Zhang HK, Huang PQ. Enantioselective syntheses of rigidiusculamides A and B: revision of the relative stereochemistry of rigidiusculamide A. Chemistry, An Asian Journal. 7: 504-18. PMID 22315233 DOI: 10.1002/Asia.201100809 |
0.323 |
|
| 2012 |
Liu XK, Zheng X, Ruan YP, Ma J, Huang PQ. One-pot reductive coupling of N-acylcarbamates with activated alkenes: application to the asymmetric synthesis of pyrrolo[1,2-a]azepin-5-one ring system and (-)-xenovenine. Organic & Biomolecular Chemistry. 10: 1275-84. PMID 22183493 DOI: 10.1039/C1Ob06697H |
0.414 |
|
| 2012 |
Xiao K, Huang Y, Huang P, 黄培强. General Direct Transformation of Secondary Amides to Ketones via Amide Activation Acta Chimica Sinica. 70: 1917. DOI: 10.6023/A12080542 |
0.32 |
|
| 2012 |
Zhang H, Xu S, Zhuang J, Ye J, Huang P. A flexible enantioselective approach to 3,4-dihydroxyprolinol derivatives by SmI2-mediated reductive coupling of chiral nitrone with ketones/aldehydes Tetrahedron. 68: 6656-6664. DOI: 10.1016/J.Tet.2012.06.006 |
0.432 |
|
| 2012 |
Liao J, Xiao K, Zheng X, Huang P. A concise and divergent approach to radicamine B and hyacinthacine A(3) based on a step-economic transformation Tetrahedron. 68: 5297-5302. DOI: 10.1016/J.Tet.2012.01.085 |
0.303 |
|
| 2012 |
Zhuang J, Ye J, Zhang H, Huang P. An unexpected high erythro-selection in the Grignard reaction with an N,O-acetal: a concise asymmetric synthesis of indolizidine alkaloid (−)-2-epi-lentiginosine Tetrahedron. 68: 1750-1755. DOI: 10.1016/J.Tet.2011.12.063 |
0.407 |
|
| 2012 |
Chen J, Wang A, Huo H, Huang P. Progress on the total synthesis of natural products in China: From 2006 to 2010 Science China-Chemistry. 55: 1175-1212. DOI: 10.1007/S11426-012-4534-9 |
0.364 |
|
| 2012 |
Zheng J, Lan H, Yang R, Peng Q, Xiao Z, Tuo S, Hu K, Xiang Y, Wei Z, Zhang Z, Huang P. Asymmetric Syntheses of the Sex Pheromones of Pine Sawflies, Their Homologs and Stereoisomers Helvetica Chimica Acta. 95: 1799-1808. DOI: 10.1002/Hlca.201200341 |
0.307 |
|
| 2012 |
Wang Z, Zheng J, Huang P. Cover Picture: Asymmetric Synthesis of Both Enantiomers of Disparlure (Chin. J. Chem. 1/2012) Chinese Journal of Chemistry. 30: 1-1. DOI: 10.1002/Cjoc.201290000 |
0.416 |
|
| 2012 |
Dai X, Huang P. A Short and Flexible Synthetic Approach to the Naturally Occurring Racemic Neoclausenamide and Its Analogs Chinese Journal of Chemistry. 30: 1953-1956. DOI: 10.1002/Cjoc.201200660 |
0.312 |
|
| 2012 |
Wang Z, Zheng J, Huang P. Asymmetric Synthesis of Both Enantiomers of Disparlure Chinese Journal of Chemistry. 30: 23-28. DOI: 10.1002/Cjoc.201100482 |
0.331 |
|
| 2012 |
Xiao K, Wang A, Huang Y, Huang P. Cover Picture: Versatile and Direct Transformation of Secondary Amides into Ketones by Deaminative Alkylation with Organocerium Reagents (Asian J. Org. Chem. 2/2012) Asian Journal of Organic Chemistry. 1: 93-93. DOI: 10.1002/Ajoc.201290005 |
0.367 |
|
| 2012 |
Wang Y, Ou W, Xie L, Ye J, Huang P. Towards Reaction Control: cis-Diastereoselective Reductive Dehydroxylation of 5-Alkyl-4-Benzyloxy-5-Hydroxy-2-Pyrrolidinones Asian Journal of Organic Chemistry. 1: 359-365. DOI: 10.1002/Ajoc.201200113 |
0.407 |
|
| 2012 |
Xiao K, Wang A, Huang Y, Huang P. Versatile and Direct Transformation of Secondary Amides into Ketones by Deaminative Alkylation with Organocerium Reagents Asian Journal of Organic Chemistry. 1: 130-132. DOI: 10.1002/Ajoc.201200066 |
0.477 |
|
| 2011 |
Chen BS, Yang LH, Ye JL, Huang T, Ruan YP, Fu J, Huang PQ. Diastereoselective synthesis and bioactivity of long-chain anti-2-amino-3-alkanols. European Journal of Medicinal Chemistry. 46: 5480-6. PMID 21955681 DOI: 10.1016/J.Ejmech.2011.09.010 |
0.309 |
|
| 2011 |
Tuo SC, Ye JL, Wang AE, Huang SY, Huang PQ. Concise asymmetric total synthesis of 9-epi-sessilifoliamide J. Organic Letters. 13: 5270-3. PMID 21879702 DOI: 10.1021/Ol202140Y |
0.342 |
|
| 2011 |
Ruan ST, Luo JM, Du Y, Huang PQ. Asymmetric vinylogous Mannich reactions: a versatile approach to functionalized heterocycles. Organic Letters. 13: 4938-41. PMID 21854016 DOI: 10.1021/Ol2020384 |
0.355 |
|
| 2011 |
Liu XK, Qiu S, Xiang YG, Ruan YP, Zheng X, Huang PQ. SmI2-mediated radical cross-couplings of α-hydroxylated aza-hemiacetals and N,S-acetals with α,β-unsaturated compounds: asymmetric synthesis of (+)-hyacinthacine A2, (-)-uniflorine A, and (+)-7-epi-casuarine. The Journal of Organic Chemistry. 76: 4952-63. PMID 21574569 DOI: 10.1021/Jo200600N |
0.417 |
|
| 2011 |
Lan HQ, Ye JL, Wang AE, Ruan YP, Huang PQ. A flexible asymmetric approach to methyl 5-alkyltetramates and its application in the synthesis of cytotoxic marine natural product belamide A. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 958-68. PMID 21226113 DOI: 10.1002/Chem.201002063 |
0.389 |
|
| 2011 |
Lin GJ, Zheng X, Huang PQ. A new method for the construction of the hydroxylated tropane skeleton: enantioselective synthesis of (-)-Bao Gong Teng A. Chemical Communications (Cambridge, England). 47: 1545-7. PMID 21107467 DOI: 10.1039/C0Cc04371K |
0.448 |
|
| 2011 |
Xiao Z, Liu L, Liu C, Huang P. A Flexible Approach to Protected (4S,5S)-5-Alkyl-1-benzyl-4-benzyloxy-2-pyrrolidinones Synthetic Communications. 41: 2036-2043. DOI: 10.1080/00397911.2010.495827 |
0.317 |
|
| 2011 |
Huang P, Du Y, Huang H, Liu H, Ruan Y. Studies towards the Total Asymmetric Synthesis of the Pentacyclic Indole Alkaloid Arboflorine: Asymmetric Synthesis of a Key Intermediate Synlett. 2011: 565-568. DOI: 10.1055/S-0030-1259521 |
0.409 |
|
| 2011 |
Zheng J, Liu H, Zhang Y, Zhao W, Tong J, Ruan Y, Huang P. A study on the racemization step in the synthesis of pyrrolidinols via cyclic α-hydroxyimides Tetrahedron-Asymmetry. 22: 257-263. DOI: 10.1016/J.Tetasy.2011.01.012 |
0.436 |
|
| 2011 |
Yang C, Bao Y, Liang P, Ye J, Wang A, Huang P. A new approach to the C28 fatty acid chain of the marine natural products schulzeines B and C: a concise diastereoselective total synthesis of(−)-schulzeine B Tetrahedron. 67: 6281-6288. DOI: 10.1016/J.Tet.2011.06.023 |
0.366 |
|
| 2011 |
Zhang H, Li X, Huang H, Huang P. Asymmetric syntheses of (8R,8aS)- and (8R,8aR)-8-hydroxy-5-indolizidinones: Two promising oxygenated indolizidine building blocks Science China-Chemistry. 54: 737-744. DOI: 10.1007/S11426-011-4256-4 |
0.339 |
|
| 2011 |
Teng B, Zheng J, Huang H, Huang P. Enantioselective Synthesis of Glutarimide Alkaloids Cordiarimides A, B, Crotonimides A, B, and Julocrotine Chinese Journal of Chemistry. 29: 1312-1318. DOI: 10.1002/Cjoc.201180248 |
0.335 |
|
| 2010 |
Xiao KJ, Wang Y, Ye KY, Huang PQ. Versatile one-pot reductive alkylation of lactams/amides via amide activation: application to the concise syntheses of bioactive alkaloids (±)-bgugaine, (±)-coniine, (+)-preussin, and (-)-cassine. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 12792-6. PMID 20938943 DOI: 10.1002/Chem.201002054 |
0.322 |
|
| 2010 |
Xu CP, Xiao ZH, Zhuo BQ, Wang YH, Huang PQ. Efficient and chemoselective alkylation of amines/amino acids using alcohols as alkylating reagents under mild conditions. Chemical Communications (Cambridge, England). 46: 7834-6. PMID 20830335 DOI: 10.1039/C0Cc01487G |
0.34 |
|
| 2010 |
Yang RF, Huang PQ. Studies towards an enantioselective total synthesis of sarain A: a concise asymmetric construction of the diazatricyclic core. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 10319-22. PMID 20669196 DOI: 10.1002/Chem.201001582 |
0.358 |
|
| 2010 |
Lan HQ, Ruan YP, Huang PQ. The first enantioselective synthesis of cytotoxic marine natural product palau'imide and assignment of its C-20 stereochemistry. Chemical Communications (Cambridge, England). 46: 5319-21. PMID 20556298 DOI: 10.1039/C0Cc00452A |
0.435 |
|
| 2010 |
Du Y, Zheng JF, Wang ZG, Jiang LJ, Ruan YP, Huang PQ. A concise, protection-free and divergent approach for the enantioselective syntheses of two pheromonal epoxide components of the fall webworm moth and other species. The Journal of Organic Chemistry. 75: 4619-22. PMID 20507127 DOI: 10.1021/Jo1007042 |
0.381 |
|
| 2010 |
Fu R, Ye JL, Dai XJ, Ruan YP, Huang PQ. Asymmetric synthesis of the cytotoxic marine natural product (+)-awajanomycin and its C-11 epimer. The Journal of Organic Chemistry. 75: 4230-43. PMID 20507081 DOI: 10.1021/Jo100744C |
0.353 |
|
| 2010 |
Liu JJ, Zeng HN, Zhang LR, Zhan YY, Chen Y, Wang Y, Wang J, Xiang SH, Liu WJ, Wang WJ, Chen HZ, Shen YM, Su WJ, Huang PQ, Zhang HK, et al. A unique pharmacophore for activation of the nuclear orphan receptor Nur77 in vivo and in vitro. Cancer Research. 70: 3628-37. PMID 20388790 DOI: 10.1158/0008-5472.Can-09-3160 |
0.311 |
|
| 2010 |
Liu G, Wu TJ, Ruan YP, Huang PQ. A flexible approach to azasugars: asymmetric total syntheses of (+)-castanospermine, (+)-7-deoxy-6-epi-castanospermine, and (+)-1-epi-castanospermine. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 5755-68. PMID 20379975 DOI: 10.1002/Chem.200903490 |
0.326 |
|
| 2010 |
Xiao KJ, Luo JM, Ye KY, Wang Y, Huang PQ. Direct, one-pot sequential reductive alkylation of lactams/amides with Grignard and organolithium reagents through lactam/amide activation. Angewandte Chemie (International Ed. in English). 49: 3037-40. PMID 20301159 DOI: 10.1002/Ange.201000652 |
0.356 |
|
| 2010 |
Xiang S, Xu J, Yuan H, Huang P. Amide Activation by Tf2O: Reduction of Amides to Amines by NaBH4 under Mild Conditions Synlett. 2010: 1829-1832. DOI: 10.1055/S-0030-1258111 |
0.326 |
|
| 2010 |
Ye Z, Chen J, Meng W, Huang P. N-Benzyloxymalimide for an easy access to 5-alkyl-3-pyrrolin-2-ones: asymmetric synthesis of the mixed imide substructure of the potent immunosuppressant microcolin B Tetrahedron-Asymmetry. 21: 895-902. DOI: 10.1016/J.Tetasy.2010.04.063 |
0.379 |
|
| 2010 |
Wu S, Ruan Y, Zheng X, Huang P. Samarium diiodide-mediated reductive couplings of chiral nitrones with aldehydes/ketones and acyl chlorides Tetrahedron. 66: 1653-1660. DOI: 10.1016/J.Tet.2010.01.011 |
0.468 |
|
| 2010 |
Jiang L, Teng B, Zheng J, Ye J, Huang P. Bis-Lewis acids-catalyzed highly diastereoselective one-pot reductive dehydroxylation of chiral N,O-acetals Tetrahedron. 66: 172-175. DOI: 10.1016/J.Tet.2009.11.003 |
0.354 |
|
| 2010 |
Zheng X, Zhu W, Huang P. Concise synthesis of two advanced intermediates for the asymmetric synthesis of polyhydroxylated indolizidine alkaloids Science China-Chemistry. 53: 1914-1920. DOI: 10.1007/S11426-010-4065-1 |
0.482 |
|
| 2010 |
Zhang H, Lin Z, Huang H, Huo H, Huang Y, Ye J, Huang P. Enantioselective Synthesis of the Diazatricyclic Core of Alkaloid TAN1251C via an Iodoaminocyclization Reaction Chinese Journal of Chemistry. 28: 1717-1724. DOI: 10.1002/Cjoc.201090290 |
0.431 |
|
| 2010 |
Huang P, Wu T, Ye J. A Flexible Approach to the γ‐Amino‐β‐hydroxy Acid Moiety of Hapalosin Chinese Journal of Chemistry. 21: 723-726. DOI: 10.1002/Cjoc.20030210704 |
0.426 |
|
| 2010 |
Chen M, He M, Huang L, Ruan Y, Huang P. A Versatile Approach for the Asymmetric Synthesis of 3‐Alkyl‐isoindolin‐1‐ones Chinese Journal of Chemistry. 20: 1149-1153. DOI: 10.1002/Cjoc.20020201105 |
0.409 |
|
| 2009 |
Xiang YG, Wang XW, Zheng X, Ruan YP, Huang PQ. One-pot cross-coupling of N-acyl N,O-acetals with alpha,beta-unsaturated compounds. Chemical Communications (Cambridge, England). 7045-7. PMID 19904389 DOI: 10.1039/B915488D |
0.358 |
|
| 2009 |
Fu R, Chen J, Guo LC, Ye JL, Ruan YP, Huang PQ. Asymmetric total synthesis of (-)-awajanomycin. Organic Letters. 11: 5242-5. PMID 19842705 DOI: 10.1021/Ol902180T |
0.442 |
|
| 2009 |
Lin GJ, Huang PQ. A concise and fully selective synthesis of the ant venom alkaloid (3S,5R,8S,9S)-3-butyl-5-propyl-8-hydroxyindolizidine. Organic & Biomolecular Chemistry. 7: 4491-5. PMID 19830300 DOI: 10.1039/B912190K |
0.434 |
|
| 2009 |
Chen J, Huang PQ, Queneau Y. Enantioselective synthesis of the R-enantiomer of the feeding deterrent (S)-ypaoamide. The Journal of Organic Chemistry. 74: 7457-63. PMID 19746925 DOI: 10.1021/Jo901557H |
0.446 |
|
| 2009 |
Wu SF, Zheng X, Ruan YP, Huang PQ. A new approach to 3-hydroxyprolinol derivatives by samarium diiodide-mediated reductive coupling of chiral nitrone with carbonyl compounds. Organic & Biomolecular Chemistry. 7: 2967-75. PMID 19582307 DOI: 10.1039/B906224F |
0.448 |
|
| 2009 |
Wei Z, Lan H, Zheng J, Huang P. New and Concise Approach to (R)-α-Lipoic Acid Synthetic Communications. 39: 691-701. DOI: 10.1080/00397910802431073 |
0.406 |
|
| 2009 |
Jiang L, Lan H, Zheng J, Ye J, Huang P. A Flexible Approach to Methyl (5S)-5-Alkyltetramate Derivatives Synlett. 2009: 297-301. DOI: 10.1055/S-0028-1087672 |
0.373 |
|
| 2009 |
Xiang S, Yuan H, Huang P. A versatile approach to cis-5-substituted 4-hydroxy-2-pyrrolidinones: asymmetric synthesis of angiogenesis inhibitor streptopyrrolidine Tetrahedron-Asymmetry. 20: 2021-2026. DOI: 10.1016/J.Tetasy.2009.08.018 |
0.437 |
|
| 2009 |
Xiao K, Liu L, Huang P. An enantioselective synthesis of (+)-azimic acid Tetrahedron-Asymmetry. 20: 1181-1184. DOI: 10.1016/J.Tetasy.2009.04.008 |
0.451 |
|
| 2009 |
Fu R, Du Y, Li Z, Xu W, Huang P. Asymmetric syntheses of 6-deoxyfagomin, d-deoxyrhamnojirimycin, and d-rhamnono-1,5-lactam Tetrahedron. 65: 9765-9771. DOI: 10.1016/J.Tet.2009.09.083 |
0.351 |
|
| 2009 |
Liu L, Xiao K, Huang P. Chemo- and diastereoselective control for a flexible approach to (5S,6S)-6-alkyl-5-benzyloxy-2-piperidinones Tetrahedron. 65: 3834-3841. DOI: 10.1016/J.Tet.2009.03.021 |
0.316 |
|
| 2009 |
Zheng X, Chen G, Ruan Y, Huang P. Generation and α-hydroxyalkylation of a novel 3-piperidinol N -α-carbanion intermediate Science China-Chemistry. 52: 1631-1638. DOI: 10.1007/S11426-009-0229-2 |
0.386 |
|
| 2008 |
Yu D, Xu W, Liu L, Huang P. First asymmetric synthesis of piperidine alkaloid (-)-morusimic acid D Synlett. 2008: 1189-1192. DOI: 10.1055/S-2008-1072737 |
0.454 |
|
| 2008 |
Lin G, Luo S, Zheng X, Ye J, Huang P. Enantiodivergent synthesis of trans-3,4-disubstituted succinimides by SmI2-mediated Reformatsky-type reaction Tetrahedron Letters. 49: 4007-4010. DOI: 10.1016/J.Tetlet.2008.04.090 |
0.462 |
|
| 2008 |
Wu T, Huang P. A concise approach to (+)-1-epi-castanospermine Tetrahedron Letters. 49: 383-386. DOI: 10.1016/J.Tetlet.2007.11.033 |
0.457 |
|
| 2008 |
Liu G, Meng J, Feng C, Huang P. Asymmetric syntheses of (-)-epi-pseudoconhydrine and (-)-5-hydroxysedamine based on a cis-diastereoselective 1,4-asymmetric induction Tetrahedron-Asymmetry. 19: 1297-1303. DOI: 10.1016/J.Tetasy.2008.05.002 |
0.379 |
|
| 2008 |
Liu L, Peng Q, Huang P. A new approach for the asymmetric synthesis of (2S,3S)-3-hydroxypipecolic acid Tetrahedron-Asymmetry. 19: 1200-1203. DOI: 10.1016/J.Tetasy.2008.04.031 |
0.415 |
|
| 2008 |
Zhou X, Zhang P, Ye J, Huang P. A versatile approach to (4S,5R)-4-benzyloxy-5-(α-hydroxyalkyl)-2-pyrrolidinones: Experimental evidences to the computational predictions Comptes Rendus Chimie. 11: 5-18. DOI: 10.1016/J.Crci.2007.02.018 |
0.441 |
|
| 2007 |
Zheng JF, Chen W, Huang SY, Ye JL, Huang PQ. A divergent asymmetric approach to aza-spiropyran derivative and (1S,8aR)-1-hydroxyindolizidine. Beilstein Journal of Organic Chemistry. 3: 41. PMID 17996045 DOI: 10.1186/1860-5397-3-41 |
0.353 |
|
| 2007 |
Zhou X, Liu WJ, Ye JL, Huang PQ. Complementary stereocontrolled approaches to 2-pyrrolidinones bearing a vicinal amino diol subunit with three continuous chiral centers: a formal asymmetric synthesis of (-)-detoxinine. The Journal of Organic Chemistry. 72: 8904-9. PMID 17949109 DOI: 10.1021/Jo7018784 |
0.44 |
|
| 2007 |
Dai CF, Cheng F, Xu HC, Ruan YP, Huang PQ. Diversity-oriented asymmetric synthesis of hapalosin: construction of three small C9/C4/C3-modified hapalosin analogue libraries. Journal of Combinatorial Chemistry. 9: 386-94. PMID 17358084 DOI: 10.1021/Cc060166H |
0.302 |
|
| 2007 |
Ye JL, Huang PQ, Lu X. Mechanism for the regioselective asymmetric addition of grignard reagents to malimides: A computational exploration. The Journal of Organic Chemistry. 72: 35-42. PMID 17194079 DOI: 10.1021/Jo0613683 |
0.405 |
|
| 2007 |
Liu L, Huang P, 黄培强. S(N)2 reaction of 2-substituted 3-piperidinol mesylate with retention of configuration: application to the asymmetric synthesis of (2R,3S)-CP-99,994 (vol 17, pg 3265, 2006) Tetrahedron-Asymmetry. 18: 155. DOI: 10.1016/J.Tetasy.2007.01.016 |
0.436 |
|
| 2007 |
Zhou X, Liu W, Ye J, Huang P. A versatile approach to pyrrolidine azasugars and homoazasugars based on a highly diastereoselective reductive benzyloxymethylation of protected tartarimide Tetrahedron. 63: 6346-6357. DOI: 10.1016/J.Tet.2007.02.087 |
0.404 |
|
| 2007 |
Chen H, Chen L, Huang P, Zhang H, Zhou Z, Tsai K. Expeditious biomimetically-inspired approaches to racemic homocitric acid lactone and per-homocitrate Tetrahedron. 63: 2148-2152. DOI: 10.1016/J.Tet.2006.12.092 |
0.367 |
|
| 2007 |
Huang P, Chen G, Zheng X. A new synthesis of alkaloid (S)-3-hydroxypiperidin-2-one and its O-TBS protected derivative Journal of Heterocyclic Chemistry. 44: 499-501. DOI: 10.1002/Jhet.5570440239 |
0.43 |
|
| 2006 |
Huang PQ, Guo ZQ, Ruan YP. A versatile approach for the asymmetric syntheses of (1R,9aR)-epiquinamide and (1R,9aR)-homopumiliotoxin 223G. Organic Letters. 8: 1435-8. PMID 16562910 DOI: 10.1021/Ol0602203 |
0.451 |
|
| 2006 |
Liu L, Huang P. F3B · OEt2‐Promoted Intramolecular Si to C Phenyl Group Migration: A Highly Diastereoselective Synthesis of (4S,5S)‐4‐Hydroxy‐5‐phenyl‐2‐pyrrolidinone Synthetic Communications. 36: 1131-1139. DOI: 10.1080/00397910500503538 |
0.39 |
|
| 2006 |
Huang P. Asymmetric Synthesis of Hydroxylated Pyrrolidines, Piperidines and Related Bioactive Compounds: From N-Acyliminium Chemistry to N-α-Carbanion Chemistry Synlett. 2006: 1133-1149. DOI: 10.1055/S-2006-941565 |
0.428 |
|
| 2006 |
Zhou X, Huang P. A Versatile Approach to Protected (4S,5R)-4-Hydroxy-5-(α-hydroxyalkyl)-2-pyrrolidinones Synlett. 2006: 1235-1239. DOI: 10.1055/S-2006-939695 |
0.452 |
|
| 2006 |
Liu L, Huang P. SN2 reaction of 2-substituted 3-piperidinol mesylate with retention of configuration: application to the asymmetric synthesis of (2R,3S)-CP-99,994 Tetrahedron-Asymmetry. 17: 3265-3272. DOI: 10.1016/J.Tetasy.2006.12.009 |
0.459 |
|
| 2006 |
Feng C, Chen J, Ye J, Ruan Y, Zheng X, Huang P. Syntheses of enantio-enriched chiral building blocks from L-glutamic acid Tetrahedron. 62: 7459-7465. DOI: 10.1016/J.Tet.2006.05.013 |
0.413 |
|
| 2006 |
Wei B, Chen J, Huang P. A new approach for the asymmetric syntheses of 2-epi-deoxoprosopinine and azasugar derivatives Tetrahedron. 62: 190-198. DOI: 10.1016/J.Tet.2005.09.112 |
0.456 |
|
| 2005 |
Ruan YP, Wei BG, Xu XQ, Liu G, Yu DS, Liu LX, Huang PQ. Detailed studies on the enantioselective synthesis and HPLC enantioseparation of N-protected 3-hydroxyglutarimides. Chirality. 17: 595-9. PMID 16200536 DOI: 10.1002/Chir.20205 |
0.451 |
|
| 2005 |
Zheng X, Feng CG, Ye JL, Huang PQ. Samarium diiodide promoted generation and asymmetric hydroxyalkylation of N,O-diprotected (3S)-3-pyrrolidinol 2-carbanions. Organic Letters. 7: 553-6. PMID 15704892 DOI: 10.1021/Ol047733Z |
0.41 |
|
| 2005 |
Tang T, Ruan Y, Ye J, Huang P. A Flexible Carbanionic Approach to Protected trans-(2R,3S)-2-Substituted 3-Aminopyrrolidines: Application to the Asymmetric Synthesis of (+)-Absouline Synlett. 2005: 231-234. DOI: 10.1055/S-2004-837194 |
0.448 |
|
| 2005 |
Huang P, Li Z. Asymmetric synthesis of (S)-homocitric acid lactone Tetrahedron-Asymmetry. 16: 3367-3370. DOI: 10.1016/J.Tetasy.2005.09.009 |
0.415 |
|
| 2005 |
Chen M, He M, Zhou X, Huang L, Ruan Y, Huang P. Studies on the diastereoselective reductive alkylation of (R)-phenylglycinol derived phthalimide: observation of stereoelectronic effects Tetrahedron. 61: 1335-1344. DOI: 10.1016/J.Tet.2004.10.109 |
0.434 |
|
| 2004 |
Liu LX, Ruan YP, Guo ZQ, Huang PQ. A general approach to (5S,6R)-6-alkyl-5-benzyloxy-2-piperidinones: application to the asymmetric syntheses of neurokinin substance P receptor antagonist (-)-L-733,061 and (-)-deoxocassine. The Journal of Organic Chemistry. 69: 6001-9. PMID 15373484 DOI: 10.1021/Jo049166Z |
0.372 |
|
| 2004 |
Huang PQ, Lan HQ, Zheng X, Ruan YP. A concise asymmetric synthesis of (2S,3S,7S)-3,7-dimethylpentadecan-2-yl Acetate and propionate, the sex pheromones of pine sawflies. The Journal of Organic Chemistry. 69: 3964-7. PMID 15153034 DOI: 10.1021/Jo0497961 |
0.384 |
|
| 2004 |
Zheng JF, Jin LR, Huang PQ. Enantiodivergent synthesis of both enantiomers of marine alkaloids haliclorensin and isohaliclorensin, a constituent of halitulin. Organic Letters. 6: 1139-42. PMID 15040742 DOI: 10.1021/Ol049887K |
0.431 |
|
| 2004 |
Ye J, Tang X, Huang P, 黄培强. Further studies on the reductive-alkylation of chiral endo-himimide derived from (R)-phenylglycinol Arkivoc. 2004. DOI: 10.3998/Ark.5550190.0005.906 |
0.356 |
|
| 2004 |
Huang P, Huang H. An Improved Asymmetric Synthesis of Unusual Amino Acid (2S,3S)‐3‐Hydroxyproline Synthetic Communications. 34: 1377-1382. DOI: 10.1081/Scc-120030686 |
0.393 |
|
| 2004 |
Ruan Y, Chen M, He M, Zhou X, Huang P. A Practical Two‐Step Synthesis of 3‐Alkyl‐2,3‐dihydro‐1H‐isoindolin‐1‐ones Synthetic Communications. 34: 853-861. DOI: 10.1081/Scc-120028358 |
0.373 |
|
| 2004 |
Huang P, Deng J. A Flexible Approach for the Asymmetric Synthesis of N-Protected (R)-5-Alkyl Tetramates and (R)-5-Alkyl Tetramic Acid Derivatives Synlett. 2004: 247-250. DOI: 10.1055/S-2003-44968 |
0.388 |
|
| 2004 |
Meng W, Wu T, Zhang H, Huang P. Asymmetric syntheses of protected (2S,3S,4S)-3-hydroxy-4-methylproline and 4 ‘-tert-butoxyamido-2 ‘-deoxythymidine Tetrahedron-Asymmetry. 15: 3899-3910. DOI: 10.1016/J.Tetasy.2004.10.030 |
0.348 |
|
| 2004 |
Du J, Huang H, Huang P. A novel approach to the Geissman–Waiss lactone and a key intermediate in the synthesis of pyrrolidine trans-lactones Tetrahedron: Asymmetry. 15: 3461-3466. DOI: 10.1016/J.Tetasy.2004.09.020 |
0.476 |
|
| 2004 |
Chen M, Zhou X, He M, Ruan Y, Huang P. A versatile approach for the asymmetric synthesis of 3-alkyl-2,3-dihydro-1H-isoindolin-1-ones Tetrahedron. 60: 1651-1657. DOI: 10.1016/J.Tet.2003.11.092 |
0.368 |
|
| 2003 |
Huang PQ, Wu TJ, Ruan YP. A flexible approach to (S)-5-alkyl tetramic acid derivatives: application to the asymmetric synthesis of (+)-preussin and protected (3S,4S)-AHPPA. Organic Letters. 5: 4341-4. PMID 14601995 DOI: 10.1021/Ol035617A |
0.43 |
|
| 2003 |
Huang PQ, Liu LX, Wei BG, Ruan YP. Asymmetric synthesis of (+)-L-733, 060 and (+)-CP-99, 994 based on a new chiral 3-piperidinol synthon. Organic Letters. 5: 1927-9. PMID 12762688 DOI: 10.1021/Ol034505G |
0.378 |
|
| 2003 |
Huang P, 黄培强, Zheng X. An improved formal total synthesis of (-)-anisomycin Arkivoc. 2003. DOI: 10.3998/Ark.5550190.0004.202 |
0.387 |
|
| 2003 |
Huang P, Zheng X, Wei H. Synthesis of (S)-vasicol and (S)-3-hydroxy-2-pyrrolidinone Heterocycles. 60: 1833-1841. DOI: 10.3987/Com-03-9800 |
0.377 |
|
| 2003 |
Huang P, Wei B, Ruan Y. Asymmetric Synthesis of AntimalarialAlkaloids (+)-Febrifugine and (+)-Isofebrifugine Synlett. 2003: 1663-1667. DOI: 10.1055/S-2003-40988 |
0.439 |
|
| 2003 |
He B, Wu T, Yu X, Huang P. A flexible non-amino acid-based formal asymmetric synthesis of naturally occurring (2R,3S)-2-aminotetradeca-5,7-dien-3-ol: observation of a remarkable protecting group effect Tetrahedron-Asymmetry. 14: 2101-2108. DOI: 10.1016/S0957-4166(03)00442-7 |
0.45 |
|
| 2002 |
Zheng X, Huang PQ, Ruan YP, Lee AW, Chan WH. A new approach for asymmetric synthesis of (R)-3-methylpyrrolidine alkaloids from (S)-malic acid. Natural Product Letters. 16: 53-6. PMID 11942683 DOI: 10.1080/1057563029001/4854 |
0.356 |
|
| 2001 |
Huang P, Zheng X, Deng X. DIBAL–H–H2NR and DIBAL–H–HNR1R2·HCl complexes for efficient conversion of lactones and esters to amides Tetrahedron Letters. 42: 9039-9041. DOI: 10.1016/S0040-4039(01)01933-5 |
0.415 |
|
| 2000 |
Huang P, 黄培强, Tang X, Chen A, 陈安奇. An alternative stereoselective synthesis of protected trans-5-alkyl-4-hydroxy-2-pyrrolidinones Synthetic Communications. 30: 2259-2268. DOI: 10.1080/00397910008086864 |
0.483 |
|
| 1999 |
Jin L, Wu H, Wu H, Huang P, Jung K, Lim H. Enantioselective Synthesis of Pyrrolydinonyl Thymine Nucleoside Analogues Chemistry Letters. 28: 687-688. DOI: 10.1246/Cl.1999.687 |
0.427 |
|
| 1998 |
Huang P, 黄培强, Wang S, Ruan Y, 阮源萍, Gao J, 高景星. A new approach to (-)-anisomycin Natural Product Letters. 11: 101-106. DOI: 10.1080/10575639808041204 |
0.461 |
|
| 1997 |
Xu P, 许翩翩, Gao J, 高景星, Wang W, 王文国, Chen Z, 陈忠, Huang P, 黄培强, Wan H, 万惠霖, Tsai K, 蔡启瑞. Synthesis, Characterization and Catalytic Properties of New Diamino/Diphosphine Ruthenium Complexes Acta Physico-Chimica Sinica. 13: 484-488. DOI: 10.3866/Pku.Whxb19970602 |
0.337 |
|
| Show low-probability matches. |