scholarly article | Q13442814 |
P356 | DOI | 10.1002/CHEM.201702008 |
P8608 | Fatcat ID | release_tq3lsfrjbnfvpctywnpc3xtr2e |
P698 | PubMed publication ID | 28475819 |
P50 | author | Sherif J Kaldas | Q88006327 |
Andrei K. Yudin | Q88006329 | ||
P2093 | author name string | Rodrigo Mendoza-Sanchez | |
Kowan T V O'Keefe | |||
P2860 | cites work | Readily Available Unprotected Amino Aldehydes | Q29392929 |
Boron's journey: advances in the study and application of pharmacokinetics. | Q30394591 | ||
Imaging protein-protein interactions using fluorescence resonance energy transfer microscopy | Q30992077 | ||
Efficient synthesis and in vivo incorporation of acridon-2-ylalanine, a fluorescent amino acid for lifetime and Förster resonance energy transfer/luminescence resonance energy transfer studies | Q33698369 | ||
Using deuterium in drug discovery: leaving the label in the drug | Q34389177 | ||
Novel copper-catalyzed multicomponent cascade synthesis of iminocoumarin aryl methyl ethers | Q34856275 | ||
From synthesis to function via iterative assembly of N-methyliminodiacetic acid boronate building blocks | Q36396226 | ||
MIDA boronates are hydrolysed fast and slow by two different mechanisms. | Q37422908 | ||
Boron-containing inhibitors of synthetases | Q37836421 | ||
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Transition metal-mediated bioorthogonal protein chemistry in living cells. | Q38215435 | ||
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Boron chemistry in a new light | Q39440559 | ||
Synthesis of most polyene natural product motifs using just 12 building blocks and one coupling reaction | Q41883693 | ||
A General Protocol for the Polycondensation of Thienyl N-Methyliminodiacetic Acid Boronate Esters To Form High Molecular Weight Copolymers | Q42085799 | ||
A general solution for the 2-pyridyl problem. | Q42322782 | ||
(1-bromovinyl)-MIDA boronate: a readily accessible and highly versatile building block for small molecule synthesis | Q42797091 | ||
α-Boryl isocyanides enable facile preparation of bioactive boropeptides. | Q44802639 | ||
Highly efficient one-pot synthesis of N-sulfonylamidines by Cu-catalyzed three-component coupling of sulfonyl azide, alkyne, and amine | Q45266536 | ||
A general solution for unstable boronic acids: slow-release cross-coupling from air-stable MIDA boronates. | Q46030717 | ||
Protodeboronation of Heteroaromatic, Vinyl, and Cyclopropyl Boronic Acids: pH-Rate Profiles, Autocatalysis, and Disproportionation. | Q46525722 | ||
Base-promoted protodeboronation of 2,6-disubstituted arylboronic acids | Q46894489 | ||
Oxidative Difunctionalization of Alkenyl MIDA Boronates: A Versatile Platform for Halogenated and Trifluoromethylated α-Boryl Ketones. | Q48148739 | ||
Synthesis of Aminoboronic Acid Derivatives from Amines and Amphoteric Boryl Carbonyl Compounds. | Q48374160 | ||
Synthesis of Previously Inaccessible Borylated Heterocycle Motifs Using Novel Boron-Containing Amphoteric Molecules. | Q50960082 | ||
A Simple and Modular Strategy for Small Molecule Synthesis: Iterative Suzuki−Miyaura Coupling of B-Protected Haloboronic Acid Building Blocks | Q56681309 | ||
Mild Rh(III)-Catalyzed C–H Activation and Annulation with Alkyne MIDA Boronates: Short, Efficient Synthesis of Heterocyclic Boronic Acid Derivatives | Q57657268 | ||
P433 | issue | 41 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 9711-9715 | |
P577 | publication date | 2017-07-06 | |
P1433 | published in | Chemistry—A European Journal | Q898737 |
P1476 | title | Amphoteric Borylketenimines: Versatile Intermediates in the Synthesis of Borylated Heterocycles | |
P478 | volume | 23 |
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