Functional-group-tolerant, nickel-catalyzed cross-coupling reaction for enantioselective construction of tertiary methyl-bearing stereocenters.
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Metal-Catalyzed Carboxylation of Organic (Pseudo)halides with CO2Enantiospecific intramolecular Heck reactions of secondary benzylic ethersEnantioselective and Enantiospecific Transition-Metal-Catalyzed Cross-Coupling Reactions of Organometallic Reagents To Construct C-C BondsNickel-Catalyzed Allylic Alkylation with Diarylmethane Pronucleophiles: Reaction Development and Mechanistic Insights.Nickel-Catalyzed Activation of Acyl C-O Bonds of Methyl Esters.Stereospecific Nickel-Catalyzed Cross-Coupling Reactions of Benzylic Ethers with Isotopically-Labeled Grignard ReagentsPd(0)-catalyzed 1,1-diarylation of ethylene and allylic carbonates.Stereospecific nickel-catalyzed cross-coupling reactions of alkyl Grignard reagents and identification of selective anti-breast-cancer agents.Re-Orienting Coupling of Organocuprates with Propargyl Electrophiles from SN2' to SN2 with Stereocontrol.Enantioselective Nickel-Catalyzed Intramolecular Allylic Alkenylations Enabled by Reversible Alkenylnickel E/Z Isomerization.Stereospecific Cross Couplings To Set Benzylic, All-Carbon Quaternary Stereocenters in High Enantiopurity.Stereospecific nickel-catalyzed cross-coupling reactions of benzylic ethers and esters.A General, Simple Catalyst for Enantiospecific Cross Couplings of Benzylic Ammonium Triflates and Boronic Acids: No Phosphine Ligand RequiredStereospecific cross-coupling reactions of aryl-substituted tetrahydrofurans, tetrahydropyrans, and lactones.Cobalt co-catalysis for cross-electrophile coupling: diarylmethanes from benzyl mesylates and aryl halides.Homologated amino acids with three vicinal fluorines positioned along the backbone: development of a stereoselective synthesis.Nickel(0)-Catalyzed Hydroarylation of Styrenes and 1,3-Dienes with Organoboron Compounds.Enantioselective Copper-Catalyzed Alkylation of Quinoline N-Oxides with Vinylarenes.Nickel-Catalyzed Asymmetric Reductive Cross-Coupling To Access 1,1-Diarylalkanes.Cross-Coupling of Organolithium with Ethers or Aryl Ammonium Salts by C-O or C-N Bond Cleavage.Mechanism and Origins of Ligand-Controlled Stereoselectivity of Ni-Catalyzed Suzuki-Miyaura Coupling with Benzylic Esters: A Computational Study.Cobalt-Catalyzed Enantioselective Negishi Cross-Coupling of Racemic α-Bromo Esters with Arylzincs.Cobalt-Catalyzed Carbonylative Cross-Coupling of Alkyl Tosylates and Dienes: Stereospecific Synthesis of Dienones at Low Pressure.Ni-Catalyzed Stannylation of Aryl Esters via C-O Bond Cleavage.Direct cross-coupling of benzyl alcohols to construct diarylmethanes via palladium catalysis.Palladium-Catalyzed Asymmetric Benzylic Alkylation of Active Methylene Compounds with α-Naphthylbenzyl Carbonates and Pivalates.Stereospecific Pd-Catalyzed Intermolecular C(sp(3))-C(sp) Cross-Coupling of Diarylmethyl Carbonates and Terminal Alkynes Under Base-Free Conditions.Synthesis of 1,1'-Diarylethanes and Related Systems by Displacement of Trichloroacetimidates with Trimethylaluminum.Nickel-catalyzed enantioselective C-C bond formation through C(sp2)-O cleavage in aryl esters.Reductive coupling of benzyl oxalates with highly functionalized alkyl bromides by nickel catalysis.
P2860
Q28073303-6A8C2922-1923-4667-BF88-8B2FB50D0ADFQ33776487-9FF131C7-A8A9-41D9-804B-9F30D6E196BFQ36049587-FF6209CD-38B5-4CEC-A64F-34D9684A5489Q36716600-51B1E19E-93E4-4F0F-A959-20DC7EF7959AQ36768166-742E3350-8AC7-4E11-B0F4-5FD06925087FQ37113860-4F6EDFED-C65C-43EF-AA4D-432400BEF1D4Q37638741-82BCF6CC-00F7-41C5-892B-28269328A35FQ37709847-B596D7B4-96FB-4D0F-93BF-10D9E40937A1Q40567809-B5E81E2B-B9E3-44DC-A15A-3902ADC4F7D6Q40950927-393E5E8C-BAD9-4799-887C-45C1103DD32AQ41169168-8B3B8E7C-34F2-444E-8A1F-8DD6FA12B439Q41762404-4AC2468C-18D5-433C-BED7-613A08DFF259Q42181224-BF98C82B-755A-42CB-8051-A95AD69AF76BQ42962501-3BE627CD-C891-495A-88EA-21C8A88C3028Q43141271-20F4F647-3FCE-4580-A375-98E866C6D940Q45426004-E9E1FA6D-AE11-442E-9572-BE569763D914Q46257339-7FCF2FF1-6505-4BB4-9CC4-2340F534CB5DQ46281597-C91DE9FA-AAAF-435A-A51B-6A899FA28254Q46378705-6B61698D-7633-476C-9B3C-88918AA01045Q46475849-76B348EC-8C8A-4643-9249-ECA41BE8C9C8Q46705158-B5394C11-9479-477F-BBBA-77E683D7C3E3Q48196461-32A0D0EC-D0C1-4A41-B5C8-9AF434BF870CQ48201665-76199B22-636F-4DA0-8F8E-30B6B9D51A2BQ48253862-98B7AEF7-EEF1-46B1-91F3-C8A0144674F4Q50441680-0CB36E63-D636-48F8-B4C3-7C573A3E08B8Q51354822-6CB31ACE-F4D1-4A7E-B619-50CD56F4FF64Q51697271-CD1A5938-3ACE-4FC2-884B-FB7FB50FF769Q52686477-1F124894-EFAF-4FF6-A446-A0D1934043DFQ52970074-618E9331-4285-4B11-90E9-FAFB3EAA3DF4Q55228213-842EFEE6-0C71-4453-BBCF-0441DAE53A7C
P2860
Functional-group-tolerant, nickel-catalyzed cross-coupling reaction for enantioselective construction of tertiary methyl-bearing stereocenters.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
Functional-group-tolerant, nic ...... methyl-bearing stereocenters.
@en
Functional-group-tolerant, nic ...... methyl-bearing stereocenters.
@nl
type
label
Functional-group-tolerant, nic ...... methyl-bearing stereocenters.
@en
Functional-group-tolerant, nic ...... methyl-bearing stereocenters.
@nl
prefLabel
Functional-group-tolerant, nic ...... methyl-bearing stereocenters.
@en
Functional-group-tolerant, nic ...... methyl-bearing stereocenters.
@nl
P2093
P2860
P356
P1476
Functional-group-tolerant, nic ...... methyl-bearing stereocenters.
@en
P2093
Elizabeth C Swift
Elizabeth R Jarvo
Hanna M Wisniewska
P2860
P304
P356
10.1021/JA4034999
P407
P577
2013-06-10T00:00:00Z