scholarly article | Q13442814 |
P356 | DOI | 10.1039/C4CC04391J |
P698 | PubMed publication ID | 25054432 |
P50 | author | Yury Minko | Q85274437 |
P2093 | author name string | Ilan Marek | |
P2860 | cites work | Preparation of substituted enol derivatives from terminal alkynes and their synthetic utility | Q43145741 |
Stereocontrolled alkylative construction of quaternary carbon centers | Q43148588 | ||
Four-Component Reactions for a New Diastereoselective Synthesis of Chiral Quaternary Centers | Q44593479 | ||
NHC-promoted asymmetric β-lactone formation from arylalkylketenes and electron-deficient benzaldehydes or pyridinecarboxaldehydes | Q45140080 | ||
A concise total synthesis of (R)-puraquinonic acid | Q45764583 | ||
Merging allylic carbon-hydrogen and selective carbon-carbon bond activation | Q46136230 | ||
Enantioselective construction of quaternary stereogenic carbons by the Lewis base catalyzed additions of silyl ketene imines to aldehydes | Q46911001 | ||
All-carbon quaternary stereogenic centers in acyclic systems through the creation of several C-C bonds per chemical step | Q46933855 | ||
Stereoselective generation of E- and Z-disubstituted amide enolates. Reductive enolate formation from bicyclic thioglycolate lactams | Q49308700 | ||
Mechanisms of nucleophilic organocopper(I) reactions. | Q51491062 | ||
Stereoselective formation of alpha-quaternary stereocenters in the Mannich reaction. | Q53401516 | ||
The Preparation of Methylcopper and some Observations on the Decomposition of Organocopper Compounds | Q56271065 | ||
The Stereochemistry of the Ivanov and Reformatsky Reactions. I | Q56288425 | ||
The stereoselective generation of ester enolates | Q56288428 | ||
Stereochemical control in the ester enolate Claisen rearrangement. 1. Stereoselectivity in silyl ketene acetal formation | Q56288430 | ||
Stereoselective aldol condensations via boron enolates | Q56288431 | ||
Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates | Q56288437 | ||
Chiral Auxiliaries - Principles and Recent Applications | Q56486304 | ||
Asymmetric alkylation reactions of chiral imide enolates. A practical approach to the enantioselective synthesis of .alpha.-substituted carboxylic acid derivatives | Q56832906 | ||
Pseudoephedrine as a Practical Chiral Auxiliary for the Synthesis of Highly Enantiomerically Enriched Carboxylic Acids, Alcohols, Aldehydes, and Ketones | Q56833702 | ||
Forming all-carbon quaternary stereogenic centres in acyclic systems from alkynes | Q59070002 | ||
Absolute configuration of chirally deuterated neopentane | Q59071707 | ||
Enantioselective construction of remote quaternary stereocentres | Q33554259 | ||
The Construction of All-Carbon Quaternary Stereocenters by Use of Pd-Catalyzed Asymmetric Allylic Alkylation Reactions in Total Synthesis | Q33763459 | ||
Enantio- and diastereodivergent dual catalysis: α-allylation of branched aldehydes | Q34347757 | ||
Studies toward the synthesis of spirolides: assembly of the elaborated E-ring fragment | Q37373881 | ||
Generation of stereochemically defined tetrasubstituted enolborinates by 1,4-hydroboration of α,β-unsaturated morpholine carboxamides with (diisopinocampheyl)borane | Q37542796 | ||
[3,3]-Sigmatropic rearrangements: recent applications in the total synthesis of natural products | Q37619267 | ||
Oxenoids in organic synthesis. | Q38183253 | ||
Regio- and stereoselective carbometallation reactions of N-alkynylamides and sulfonamides | Q39908226 | ||
A concise and versatile double-cyclization strategy for the highly stereoselective synthesis and arylative dimerization of Aspidosperma alkaloids | Q41959162 | ||
A simple, scalable synthetic route to (+)- and (-)-pseudoephenamine | Q41972325 | ||
Tandem carbocupration/oxygenation of terminal alkynes | Q42405930 | ||
Pseudoephenamine: a practical chiral auxiliary for asymmetric synthesis | Q42708042 | ||
A unique approach to aldol products for the creation of all-carbon quaternary stereocentres | Q42747316 | ||
P433 | issue | 84 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 12597-12611 | |
P577 | publication date | 2014-10-01 | |
P1433 | published in | Chemical Communications | Q426303 |
P1476 | title | Stereodefined acyclic trisubstituted metal enolates towards the asymmetric formation of quaternary carbon stereocentres | |
P478 | volume | 50 |
Q48346593 | Acyclic Quaternary Carbon Stereocenters via Enantioselective Transition Metal Catalysis. |
Q58610670 | Allenoates in Enantioselective [2+2] Cycloadditions: From a Mechanistic Curiosity to a Stereospecific Transformation |
Q90510939 | Catalytic Enantioselective Synthesis of Acyclic Quaternary Centers: Palladium-Catalyzed Decarboxylative Allylic Alkylation of Fully Substituted Acyclic Enol Carbonates |
Q41594809 | Chiral ammonium betaine-catalyzed asymmetric Mannich-type reaction of oxindoles |
Q89893012 | Cu-Catalyzed Diastereo- and Enantioselective Reactions of γ,γ-Disubstituted Allyldiboron Compounds with Ketones |
Q64174733 | Cyclometalated Iridium-PhanePhos Complexes Are Active Catalysts in Enantioselective Allene-Fluoral Reductive Coupling and Related Alcohol-Mediated Carbonyl Additions That Form Acyclic Quaternary Carbon Stereocenters |
Q48107967 | Enabling the Cross-Coupling of Tertiary Organoboron Nucleophiles through Radical-Mediated Alkyl Transfer |
Q46642667 | Enantioselective Construction of Acyclic Quaternary Carbon Stereocenters: Palladium-Catalyzed Decarboxylative Allylic Alkylation of Fully Substituted Amide Enolates. |
Q42732697 | Enantioselective Formation of All-Carbon Quaternary Centers via C-H Functionalization of Methanol: Iridium-Catalyzed Diene Hydrohydroxymethylation |
Q48294382 | Enantioselective Formation of CF3-Bearing All-Carbon Quaternary Stereocenters via C-H Functionalization of Methanol: Iridium Catalyzed Allene Hydrohydroxymethylation |
Q41833646 | Enantioselective allylic alkylation of stereodefined polysubstituted copper enolates as an entry to acyclic quaternary carbon stereocentres |
Q92278178 | Palladium-catalyzed enantioselective decarboxylative allylic alkylation of fully substituted N-acyl indole-derived enol carbonates |
Q47100392 | Remote functionalization of hydrocarbons with reversibility enhanced stereocontrol |
Search more.