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Chemical Communications : Chem Comm, ISSN 1359-7345, 01/2019, Volume 55, Issue 46, pp. 6535 - 6538
Described is an efficient oxidative dearomatization of indoles with TEMPO oxoammonium salt and a broad range of nucleophiles. Under very mild conditions,... 
Indoles | Nucleophiles
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 11/2019, p. 151415
Journal Article
Chemical Communications : Chem Comm, ISSN 1359-7345, 01/2018, Volume 54, Issue 72, pp. 10112 - 10115
A direct, single synthetic homologative transformation of halostannanes into mono- or di-substituted methyl analogues is documented. Critical for the success... 
Nucleophiles | Homology | Reagents
Journal Article
SCIENCE, ISSN 0036-8075, 05/2013, Volume 340, Issue 6136, pp. 1065 - 1068
An important challenge in asymmetric synthesis is the development of fully stereodivergent strategies to access the full complement of stereoisomers of... 
ALCOHOLS | DIASTEREOSELECTIVITY | MULTIDISCIPLINARY SCIENCES | TRANSITION-METAL | ALLYLIC ALKYLATION | ORGANOCATALYSIS | NUCLEOPHILE | DERIVATIVES | EFFICIENT | TERTIARY | PHOTOREDOX CATALYSIS
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 01/2015, Volume 56, Issue 2, pp. 283 - 295
The copper-catalyzed propargylic substitution reaction has become a powerful synthetic method to prepare the compounds containing the propargylic subunit.... 
N-Nucleophiles | Copper | Asymmetric catalysis | Propargylic substitution | C-Nucleophiles | ALKYLATION | CHEMISTRY, ORGANIC | ALCOHOLS | AMINATION | BETA-KETOESTERS | COUPLING REACTIONS | AMINES | ESTERS | ACETATES | SYSTEMS | METAL | Cycloaddition | Tetrahedrons | Handles | Selectivity | Sulfur | Nucleophiles | Carbon
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 11/2019, p. 151363
Journal Article
Organic Letters, ISSN 1523-7060, 11/2018, Volume 20, Issue 21, pp. 6836 - 6839
An unprecedented (NH4)2S2O8 mediated metal-free three-component alkene oxyalkynylation using H2O or alcohol as oxygenation agent is described. Mechanistic... 
DIFUNCTIONALIZATION | ALCOHOLS | PHOTOCHEMICAL NUCLEOPHILE | STYRENES | ACIDS | ANTI-MARKOVNIKOV ADDITION | CHEMISTRY, ORGANIC | NUCLEOPHILE-OLEFIN COMBINATION | RADICALS | EFFICIENT | AROMATIC-SUBSTITUTION REACTION
Journal Article
Chemical Communications: Chem Comm, ISSN 1359-7345, 02/2017, Volume 53, Issue 12, pp. 2032 - 2035
The reaction of the methylidyne complex [W(&z.tbd; CH)Br(CO)2(dcpe)] (dcpe = 1,2-bis(dicyclohexylphosphino)ethane) with tBuLi affords the intermediate anionic... 
Nucleophiles | Methylidyne | Carbyne
Journal Article
Dalton Transactions, ISSN 1477-9226, 01/2018, Volume 47, Issue 17, pp. 5938 - 5942
Tetrazines react with OCP−1 through a reverse electron demand Diels–Alder process to produce 3,6-disubstituted-1,2,4-diazaphosphinin-5-olates. DFT calculations... 
Coordination polymers | Sodium | Nucleophiles
Journal Article
Synthesis, ISSN 0039-7881, 06/2015, Volume 47, Issue 11, pp. 1581 - 1592
Abstract A practical BF 3 ·OEt 2 -catalyzed regioselective 1,2-addition or 1,4-hetero-Michael addition of oxygen, sulfur, and nitrogen nucleo­philes to... 
paper | Michael addition | maleimide | sulfur nucleophiles | oxygen nucleophiles | nitrogen nucleophiles | boron trifluoride diethyl etherate
Journal Article
Nature Chemistry, ISSN 1755-4330, 2014, Volume 6, Issue 8, pp. 720 - 726
Journal Article
Chemical Communications: Chem Comm, ISSN 1359-7345, 03/2015, Volume 51, Issue 30, pp. 6637 - 6639
A facile access to 4-((trifluoromethyl)thio)-2,3-dihydrofurans from unprotected homopropargylic alcohols in high regioselectivity is reported. This method is... 
Nucleophiles | Alcohols | Alkynes
Journal Article
Chemical Communications: Chem Comm, ISSN 1359-7345, 01/2015, Volume 51, Issue 8, pp. 1394 - 1409
The preparation of N-containing heterocycles is always the core of synthetic chemistry. Recently, oxidative coupling between two R-H nucleophiles is gaining... 
Methodology | Coupling | Nucleophiles
Journal Article
Journal of Organic Chemistry, ISSN 0022-3263, 06/2017, Volume 82, Issue 11, p. 5552
Journal Article
Organic & Biomolecular Chemistry, ISSN 1477-0520, 01/2018, Volume 16, Issue 39, pp. 7104 - 7108
A first atom-economic [2 + 2] cycloaddition/1,6-conjugate addition cascade of yne-allenones with C-nucleophiles including 1,3-dicarbonyls and... 
Cycloaddition | Aromatic compounds | Nucleophiles | Crystallography
Journal Article
Journal of Molecular Structure, ISSN 0022-2860, 02/2020, Volume 1202, p. 127232
In an extension of the research on the nucleophilic substitution reactions of hexachlorocyclotriphosphazene ( ) with linear aliphatic primary diamines, NH -(CH... 
Ansa compounds | Bridged compounds | Spiro compounds | Base | Nucleophile
Journal Article
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