Asymmetric alkyl-alkyl cross-couplings of unactivated secondary alkyl electrophiles: stereoconvergent Suzuki reactions of racemic acylated halohydrins
about
Remote carboxylation of halogenated aliphatic hydrocarbons with carbon dioxide.Stereoconvergent amine-directed alkyl-alkyl Suzuki reactions of unactivated secondary alkyl chloridesStereoconvergent arylations and alkenylations of unactivated alkyl electrophiles: catalytic enantioselective synthesis of secondary sulfonamides and sulfonesAdvances in transition metal (Pd, Ni, Fe)-catalyzed cross-coupling reactions using alkyl-organometallics as reaction partnersA systematic investigation of quaternary ammonium ions as asymmetric phase-transfer catalysts. Synthesis of catalyst libraries and evaluation of catalyst activity.Ni(II) salts and 2-propanol effect catalytic reductive coupling of epoxides and alkynesExpanded substrate scope and improved reactivity of ether-forming cross-coupling reactions of organotrifluoroborates and acetals.Catalytic asymmetric γ-alkylation of carbonyl compounds via stereoconvergent Suzuki cross-couplings.Pd(II)-catalyzed enantioselective C-H activation of cyclopropanes.Nickel-catalyzed enantioselective cross-couplings of racemic secondary electrophiles that bear an oxygen leaving group.New directing groups for metal-catalyzed asymmetric carbon-carbon bond-forming processes: stereoconvergent alkyl-alkyl Suzuki cross-couplings of unactivated electrophiles.Enantioselective and Enantiospecific Transition-Metal-Catalyzed Cross-Coupling Reactions of Organometallic Reagents To Construct C-C BondsNickel-catalyzed cross-coupling of photoredox-generated radicals: uncovering a general manifold for stereoconvergence in nickel-catalyzed cross-couplings.Catalytic enantioselective cyclization/cross-coupling with alkyl electrophiles.sp3-sp3 Coupling reactions in the synthesis of natural products and biologically active molecules.Pinene-derived iminodiacetic acid (PIDA): a powerful ligand for stereoselective synthesis and iterative cross-coupling of C(sp3) boronate building blocks.Ni-Catalyzed C-C Couplings Using Alkyl Electrophiles.Advances in Stereoconvergent Catalysis from 2005 to 2015: Transition-Metal-Mediated Stereoablative Reactions, Dynamic Kinetic Resolutions, and Dynamic Kinetic Asymmetric Transformations.Transition metal-catalyzed alkyl-alkyl bond formation: Another dimension in cross-coupling chemistry.Design, Synthesis, and Optimization of Balanced Dual NK1/NK3 Receptor AntagonistsEnantioselective assembly of tertiary stereocenters via multicomponent chemoselective cross-coupling of geminal chloro(iodo)alkanes.Transition-Metal Catalysis of Nucleophilic Substitution Reactions: A Radical Alternative to SN1 and SN2 Processes.Nickel-catalyzed cross-coupling of potassium aryl- and heteroaryltrifluoroborates with unactivated alkyl halides.Stereospecific cross-coupling of secondary organotrifluoroborates: potassium 1-(benzyloxy)alkyltrifluoroborates.Asymmetric transition metal-catalyzed cross-coupling reactions for the construction of tertiary stereocenters.Construction of quaternary stereogenic carbon centers through copper-catalyzed enantioselective allylic cross-coupling with alkylboranes.Enantioselective Construction of Trifluoromethoxylated Stereogenic Centers by a Nickel-Catalyzed Asymmetric Suzuki-Miyaura Coupling of Secondary Benzyl Bromides.Cobalt-Catalyzed Enantioselective Negishi Cross-Coupling of Racemic α-Bromo Esters with Arylzincs.Harnessing Alkyl Amines as Electrophiles for Nickel-Catalyzed Cross Couplings via C-N Bond Activation.Highly Efficient, Convergent, and Enantioselective Synthesis of Phthioceranic Acid.Synthesis of chiral heterocycles by ligand-controlled regiodivergent and enantiospecific Suzuki Miyaura cross-coupling.Copper-Catalyzed Cross-Coupling Reaction of Organoboron Compounds with Primary Alkyl Halides and PseudohalidesOrganische Chemie 2010
P2860
Q33470414-0C2B3828-D532-44C5-9226-BC5A4617F99FQ33893047-392D0252-6B6E-4FCB-81E2-C9040AEE884FQ34120285-8C86BA49-61C0-4F99-A6C8-8207FD673088Q34788016-7DC064D3-4F98-4F2A-9BB2-93C3944A9580Q35023347-55BA941C-F4F3-4773-9300-194E87D36916Q35141026-4C5EF747-5A2E-4C40-A6DD-D40C744AE6FBQ35190156-A5DD0735-5609-4600-BBDA-893C431E2CFAQ35242174-35F26A26-72EC-4D24-8F96-BFDCA45C7C0CQ35620535-38A6FACB-2FCF-4169-ABD3-83E5DF4EE829Q35783298-71E0A17C-9842-46EE-BE16-26BFB36A4DD6Q35905842-24AA664C-0E92-4162-97A8-2EF9D8541538Q36049587-878D430A-0E85-48FA-B9F2-866824FA1E76Q36078422-48D16D4E-37D6-4A40-BAF8-1FD67B30CBA4Q37701007-B660C02A-E92B-416A-BCA2-62B7F66E1B56Q38191444-7062BB4C-C72E-46B7-B1CA-E98FBD2FB1BFQ38273207-232E4D55-E401-4260-8E2D-6E9A312DDA80Q38942612-2DA89354-34BC-455A-A075-E14A3EE9C452Q39121643-702EE62F-6212-4C7B-BA2E-4BE471B589B5Q39241610-D25DD94F-55BE-41F8-A2A3-29479A957DC2Q39787316-0CB401DF-4A88-4CF3-AD02-AA1ED5557067Q41092159-255FA276-A20D-49C1-9DBC-AA2BBDD9A581Q41162504-CA7E7657-0F9D-4AF7-82B5-0334AFD8B98CQ41840604-6EF53536-8917-48D8-9970-92A0A5D5CDC3Q42404427-1E23EB4C-EBAF-4AB6-84E8-590B2AC41AA5Q42554304-0D3594A9-F789-45D6-BDCE-4426ED3EB082Q46914306-786406C5-D8A1-4602-83E5-837B9EF54330Q48096623-3F9A1BBE-DE23-4C44-88AF-7DD30D8A5E2AQ48196461-F90F1E93-DF1A-4374-82B8-C959AE221CB4Q48343853-3FBE28E4-1F24-49B1-AB55-02EEDC57ABBEQ50962098-FDF77428-AE76-478C-856D-534703CF44D5Q52782591-5410ECBB-B0EE-44E7-BF5F-A870C89852CEQ56482603-52528744-D244-491A-A08F-D6CC951FEC74Q57742701-9AEC552F-8F6E-4E86-B5B8-F84674AD11FB
P2860
Asymmetric alkyl-alkyl cross-couplings of unactivated secondary alkyl electrophiles: stereoconvergent Suzuki reactions of racemic acylated halohydrins
description
2010 nî lūn-bûn
@nan
2010 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Asymmetric alkyl-alkyl cross-c ...... f racemic acylated halohydrins
@ast
Asymmetric alkyl-alkyl cross-c ...... f racemic acylated halohydrins
@en
Asymmetric alkyl-alkyl cross-c ...... f racemic acylated halohydrins
@nl
type
label
Asymmetric alkyl-alkyl cross-c ...... f racemic acylated halohydrins
@ast
Asymmetric alkyl-alkyl cross-c ...... f racemic acylated halohydrins
@en
Asymmetric alkyl-alkyl cross-c ...... f racemic acylated halohydrins
@nl
prefLabel
Asymmetric alkyl-alkyl cross-c ...... f racemic acylated halohydrins
@ast
Asymmetric alkyl-alkyl cross-c ...... f racemic acylated halohydrins
@en
Asymmetric alkyl-alkyl cross-c ...... f racemic acylated halohydrins
@nl
P2860
P356
P1476
Asymmetric alkyl-alkyl cross-c ...... f racemic acylated halohydrins
@en
P2093
Gregory C Fu
Nathan A Owston
P2860
P304
11908-11909
P356
10.1021/JA105924F
P407
P577
2010-09-01T00:00:00Z