Nelson Y. S. Lam

university of auckland

H指数:19

被引数:1,835

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Catalytic Enantioselective Hydrogen Atom Abstraction Enables the Asymmetric Oxidation of Meso Diols

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

IF15.6

2024-11-260

OAAI

Synthesis of the Phormidolide A Macrocycle Supports the Proposed Configurational Reassignment

ORGANIC LETTERS

IF5

2024-09-270

PRE

Palladium (II)-Catalyzed C-H Activation with Bifunctional Ligands: From Curiosity to Industrialization

双功能配体的钯 (II) 催化的c-h活化: 从好奇心到工业化

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

IF16.9

2024-03-149

PRE

Ortho-Selective amination of arene carboxylic acids via rearrangement of acyl O-hydroxylamines

CHEMICAL SCIENCE

IF7.4

2023-01-018

OAAI

An Enantioselective Suzuki-Miyaura Coupling To Form Axially Chiral Biphenols

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

IF15.6

2022-08-1532

OAAI

A Solid Support-Based Synthetic Strategy for the Site-Selective Functionalization of Peptides with Organometallic Half-Sandwich Moieties

基于固体支持物的合成策略，用于具有有机金属半夹心部分的肽的位点选择性官能化

CHEMISTRY-A EUROPEAN JOURNAL

IF3.7

2022-02-0210

PRE

Empirical Guidelines for the Development of Remote Directing Templates through Quantitative and Experimental Analyses

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

IF15.6

2022-02-0240

Palladium-Catalyzed Enantioselective β-C(sp3)-H Activation Reactions of Aliphatic Acids: A Retrosynthetic Surrogate for Enolate Alkylation and Conjugate Addition

ACCOUNTS OF CHEMICAL RESEARCH

IF17.7

2022-01-2571

A synthesis-enabled relative configurational assignment of the C31-C46 region of hemicalide

CHEMICAL COMMUNICATIONS

IF4.2

2022-01-013

A directive Ni catalyst overrides conventional site selectivity in pyridine C-H alkenylation

定向Ni催化剂在吡啶c-h烯基化中取代了常规位点选择性

NATURE CHEMISTRY

IF20.2

2021-10-1172

Mechanistic Study of Enantioselective Pd-Catalyzed C(sp3)-H Activation of Thioethers Involving Two Distinct Stereomodels

ACS CATALYSIS

IF13.1

2021-07-1916

OAAI

Advancing the Logic of Chemical Synthesis: C-H Activation as Strategic and Tactical Disconnections for C-C Bond Construction

推进化学合成的逻辑: c-h活化作为c-c键构建的战略和战术断开

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

IF16.9

2021-02-04239

OAAI

Conquering peaks and illuminating depths: developing stereocontrolled organic reactions to unlock nature's macrolide treasure trove

CHEMICAL COMMUNICATIONS

IF4.2

2021-01-0111

The Stereocontrolled Total Synthesis of Polyketide Natural Products: A Thirty-Year Journey

BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN

IF3.8

2020-11-1022

Achieving Site-Selectivity for C-H Activation Processes Based on Distance and Geometry: A Carpenter's Approach

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

IF15.6

2020-05-21259

OAAI

Total synthesis and biological evaluation of simplified aplyronine analogues as synthetically tractable anticancer agents

简化的aplyron类似物作为可合成的抗癌剂的全合成和生物学评估

CHEMICAL COMMUNICATIONS

IF4.2

2020-01-0110

OAAI

Synergism of anisotropic and computational NMR methods reveals the likely configuration of phormidolide A

CHEMICAL COMMUNICATIONS

IF4.2

2020-01-0125

OAAI

Unexpected arene ligand exchange results in the oxidation of an organoruthenium anticancer agent: the first X-ray structure of a protein-Ru(carbene) adduct (vol 54, pg 6120, 2018)

CHEMICAL COMMUNICATIONS

IF4.2

2019-01-011

OAAI

A counterintuitive stereochemical outcome from a chelation-controlled vinylmetal aldehyde addition leads to the configurational reassignment of phormidolide A

CHEMICAL COMMUNICATIONS

IF4.2

2019-01-0118

PREAI

From Catalysis to Cancer: Toward Structure-Activity Relationships for Benzimidazol-2-ylidene-Derived N-Heterocyclic-Carbene Complexes as Anticancer Agents

从催化到癌症: Benzimidazol-2-ylidene-Derived N-杂环-卡宾配合物作为抗癌剂的结构-活性关系

INORGANIC CHEMISTRY

IF4.7

2018-11-0861

PREAI

Nelson Y. S. Lam

个人简介

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