o-Iodoxybenzoic acid (IBX) as a viable reagent in the manipulation of nitrogen- and sulfur-containing substrates: scope, generality, and mechanism of IBX-mediated amine oxidations and dithiane deprotections.
about
Room-temperature aromatization of tetrahydro-β-carbolines by 2-iodoxybenzoic acid: utility in a total synthesis of eudistomin U.Cu-catalyzed cross-dehydrogenative coupling: a versatile strategy for C-C bond formations via the oxidative activation of sp(3) C-H bonds.The essence of total synthesisAllene formation by gold catalyzed cross-coupling of masked carbenes and vinylidenes.Constructing molecular complexity and diversity: total synthesis of natural products of biological and medicinal importance.Enantiospecific total synthesis of the hapalindoles, fischerindoles, and welwitindolinones via a redox economic approach.Chemistry of polyvalent iodine.Effect of Substituents and Stability of Transient Aluminum-Aminals in the Presence of Nucleophiles2-Iodoxybenzoic acid--a simple oxidant with a dazzling array of potential applications.Hypervalent iodine reagents in the total synthesis of natural products.Enantioselective total syntheses of (-)-palau'amine, (-)-axinellamines, and (-)-massadines.Oxidative dehydrogenation of C-C and C-N bonds: A convenient approach to access diverse (dihydro)heteroaromatic compounds.Potassium N-iodo p-toluenesulfonamide (TsNIK, Iodamine-T): a new reagent for the oxidation of hydrazones to diazo compoundsAn approach towards azafuranomycin analogs by gold-catalyzed cycloisomerization of allenes: synthesis of (αS,2R)-(2,5-dihydro-1H-pyrrol-2-yl)glycine.Simple copper/TEMPO catalyzed aerobic dehydrogenation of benzylic amines and anilines.The first example of a centro-symmetrical bis(imido)-bridged dinuclear cobalt(III) complex: synthesis via oxidative dehydrogenation and phenoxazinone synthase activity.Continuous-flow oxidative cyanation of primary and secondary amines using singlet oxygen.Metal-Free α-C(sp³)-H Functionalized Oxidative Cyclization of Tertiary N,N-Diaryl Amino Alcohols: Theoretical Approach for Mechanistic Pathway.Formation of C=N bonds by the release of H2: a new strategy for synthesis of imines and benzazoles.Oxidative dearomatization of phenols and anilines via lambda(3)- and lambda(5)-iodane-mediated phenylation and oxygenation.Structural Requirements of Histone Deacetylase Inhibitors: SAHA Analogs Modified on the Hydroxamic Acid.Gluco-1 H-imidazole: A New Class of Azole-Type β-Glucosidase Inhibitor.IBX-mediated oxidation of unactivated cyclic amines: application in highly diastereoselective oxidative Ugi-type and aza-Friedel-Crafts reactions.A Mechanochemical-Assisted Oxidation of Amines to Carbonyl Compounds and NitrilesMetal-Free α-C(sp3)−H Functionalized Oxidative Cyclization of TertiaryN,N-Diarylamino Alcohols: Construction ofN,N-Diarylaminotetrahydropyran ScaffoldsRuthenium-Catalyzed Oxidative Coupling of Primary Amines with Internal Alkynes through CH Bond Activation: Scope and Mechanistic Studies
P2860
Q34117592-74F531F2-DD24-44BA-9F12-9D08B32A682BQ34694674-4AA8E69A-B85D-4D7E-A9CF-014609706BC3Q35859755-3A489BB6-05AF-4002-9ECD-7B7B03F506F7Q35962898-323EC9DE-1384-4FFF-9FB3-4662EA47749CQ36186718-106595F7-40C3-4385-AC78-9ABA5E3E36E8Q37080286-DAEFA951-DD49-4888-B293-E37DC236B66CQ37318116-654266BD-D942-438C-847F-633837300BDCQ37669754-70A6A608-9B7A-4E7E-BFC3-4CB1C522CC95Q37832721-C24101F8-E231-446E-9788-44F8B0028EFDQ37914735-0AFE018C-1D6C-407F-B193-3EC154FF779AQ38433980-096EA5F0-D9D8-4765-AFBE-F9ED68AEE682Q41469033-0091626B-3AD0-49BB-AC05-F2CE89B1C292Q41787185-3ABBD7D8-4B0E-4727-96F4-504CC1DA28F8Q42921660-A5D453EC-7195-4C32-B768-41E2721ED989Q43462447-CD27D8A4-9B9D-4A81-BB41-1A8C4F5735C3Q45218854-6C8D7089-BE21-4C9E-A315-DE2BC9303FF3Q46247279-CA3E43F4-4990-4EFC-B4A3-17BC51C8774FQ46394600-AE12C064-A72F-42DB-921D-45DFDCF8CA87Q46550097-F62E1CDB-2EAA-4EBC-BBB4-A86B8337CC32Q46897251-6247ECAC-9C9B-46C2-B882-2450BB91DC19Q50862788-24CA8DB2-E589-4D15-8CAF-2F332556D4E3Q52619349-D6F78193-FEBC-43CC-90F1-23482E39959CQ53671501-90A83250-2CEC-40FB-B0FA-196B07AF098EQ57578089-A40EB0F6-13FC-49A6-8E85-6AD13FCBB897Q57712463-2880F843-4E72-4BBD-B5D5-20A4F2628E1CQ57825483-95C33B5A-3195-4359-AFFF-C3178C6555D4
P2860
o-Iodoxybenzoic acid (IBX) as a viable reagent in the manipulation of nitrogen- and sulfur-containing substrates: scope, generality, and mechanism of IBX-mediated amine oxidations and dithiane deprotections.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh-hant
name
o-Iodoxybenzoic acid (IBX) as ...... ns and dithiane deprotections.
@en
o-Iodoxybenzoic acid (IBX) as ...... ns and dithiane deprotections.
@nl
type
label
o-Iodoxybenzoic acid (IBX) as ...... ns and dithiane deprotections.
@en
o-Iodoxybenzoic acid (IBX) as ...... ns and dithiane deprotections.
@nl
prefLabel
o-Iodoxybenzoic acid (IBX) as ...... ns and dithiane deprotections.
@en
o-Iodoxybenzoic acid (IBX) as ...... ns and dithiane deprotections.
@nl
P2093
P356
P1476
o-Iodoxybenzoic acid (IBX) as ...... ns and dithiane deprotections.
@en
P2093
Casey J N Mathison
K C Nicolaou
Tamsyn Montagnon
P304
P356
10.1021/JA0400382
P407
P577
2004-04-01T00:00:00Z