about
Synthesis of 1,2,3-triazole hydrazide derivatives exhibiting anti-phytopathogenic activity.Synthesis of 1-acyl-3-isopropenylbenzimidazolone derivatives and their activity against Botrytis cinerea.Rh-catalyzed highly enantioselective hydrogenation of nitroalkenes under basic conditions.The main chemical composition and in vitro antifungal activity of the essential oils of Ocimum basilicum Linn. var. pilosum (Willd.) Benth."Carbon Assimilation" Inspired Design and Divergent Synthesis of Drimane Meroterpenoid Mimics as Novel Fungicidal Leads.Synthesis and antifungal activity of 1,2,3-triazole phenylhydrazone derivatives.Highly regioselective isomerization-hydroaminomethylation of internal olefins catalyzed by Rh complex with Tetrabi-type phosphorus ligandsHighly enantioselective hydrogenation of β,β-disubstituted nitroalkenesRhodium-catalyzed enantioselective hydrogenation of oxime acetatesCascade synthesis of fenpiprane and related pharmaceuticals via rhodium-catalyzed hydroaminomethylationRhodium-catalyzed highly regioselective hydroaminomethylation of styrenes with tetraphosphorus ligandsA novel chiral bisphosphine-thiourea ligand for asymmetric hydrogenation of β,β-disubstituted nitroalkenesEnantioselective hydrogenation of α,β-disubstituted nitroalkenesLate-Stage C-H Functionalization of Nicotinamides for the Expedient Discovery of Novel Antifungal LeadsDesign and Discovery of Novel Chiral Antifungal Amides with 2-(2-Oxazolinyl)aniline as a Promising PharmacophoreEnantioselective total synthesis, divergent optimization and preliminary biological evaluation of (indole-N-alkyl)-diketopiperazinesExpediently Scalable Synthesis and Antifungal Exploration of (+)-Yahazunol and Related Meroterpenoids
P50
Q38810681-F337318E-8B22-4B79-8878-79A37A52C8B5Q43184008-18BBD1AF-3E21-4A1F-88BE-2AE5AB9CE3CAQ45760624-2CDD9606-D2E5-47D1-8247-539579FF0961Q46167532-83ABF98D-99D6-4DBB-90E2-174E08EFA111Q48287033-5CA770EB-78E6-4C32-A7F9-2E0FF92753C4Q50446473-B731A460-1FAB-4619-AC7B-BC1458BB3944Q82848017-DACBDBA2-0D46-4C6A-89E7-27C6FA596517Q84583351-AAEBE51E-553B-45F5-AD06-1EE13A2AE90AQ85934618-5300A8AC-D03A-4495-BF42-97ABA9962D9EQ86119316-49CCE444-384C-43D2-89B1-AAA0CBBCC007Q86888620-732C8F4C-C8C8-47F1-A8B5-5BADC90DCC9FQ87142946-B88DB8A1-ECE7-4FF4-85E6-672AC1C50A8FQ88166079-8B91FB55-A9EE-46A3-A48B-EA513CF22923Q90478872-949DDBC7-D97C-4A33-82D9-C658127117ADQ90855869-327219E2-A00B-4F5C-8E5F-608006409465Q91069020-9E8486F7-CDEA-4D4B-B479-8EF30066A19EQ91400364-24F12734-64E6-48C3-93AE-1B3D8C083EC6
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Shengkun Li
@ast
Shengkun Li
@en
Shengkun Li
@es
Shengkun Li
@nl
Shengkun Li
@sl
type
label
Shengkun Li
@ast
Shengkun Li
@en
Shengkun Li
@es
Shengkun Li
@nl
Shengkun Li
@sl
altLabel
Sheng-Kun Li
@en
prefLabel
Shengkun Li
@ast
Shengkun Li
@en
Shengkun Li
@es
Shengkun Li
@nl
Shengkun Li
@sl
P1053
K-9108-2017
P106
P31
P3829
P496
0000-0001-5458-0811