syn-1,2-Amino alcohols via diastereoselective allylic C-H amination

scientific article published on 22 May 2007

syn-1,2-Amino alcohols via diastereoselective allylic C-H amination is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1021/JA071905G
P932PMC publication ID2720786
P698PubMed publication ID17516648
P5875ResearchGate publication ID6315295

P50authorM. Christina WhiteQ55252
Kenneth J FraunhofferQ125172311
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Regio- and enantioselective allylic amination of achiral allylic esters catalyzed by an iridium-phosphoramidite complexQ44252823
Direct catalytic asymmetric Mannich-type reaction of hydroxyketone using a Et2Zn/linked-BINOL complex: synthesis of either anti- or syn-beta-amino alcoholsQ44975964
Aerobic oxidative amination of unactivated alkenes catalyzed by palladiumQ45289301
Palladium(II)-catalyzed highly regio- and diastereoselective cyclization of difunctional allylic N-tosylcarbamates. A convenient synthesis of optically active 4-vinyl-2-oxazolidinones and total synthesis of 1,4-dideoxy-1,4-imino-L-xylitolQ45713709
Direct catalytic asymmetric synthesis of anti-1,2-amino alcohols and syn-1,2-diols through organocatalytic anti-Mannich and syn-aldol reactionsQ46089620
Serial ligand catalysis: a highly selective allylic C-H oxidationQ46482828
Copper(II) acetate promoted intramolecular diamination of unactivated olefinsQ46642279
N-tosyloxycarbamates as a source of metal nitrenes: rhodium-catalyzed C-H insertion and aziridination reactionsQ46746914
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A direct catalytic asymmetric mannich-type reaction to syn-amino alcoholsQ46778750
A Rh-Catalyzed C-H Insertion Reaction for the Oxidative Conversion of Carbamates to Oxazolidinones We thank Professors Brauman, Stack, Trost, and Wender for many helpful discussions. C.G.E. is the recipient of an NSF Predoctoral Fellowship. J.D.B. gQ48370443
Oxazolidinone susceptibility patterns for 2005: International Report from the Zyvox Annual Appraisal of Potency and Spectrum StudyQ48920995
Highly regioselective Pd-catalyzed intermolecular aminoacetoxylation of alkenes and evidence for cis-aminopalladation and S(N)2 C-O bond formation.Q53620588
Sequential Hydrocarbon Functionalization: Allylic C−H Oxidation/Vinylic C−H ArylationQ64113967
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A sulfoxide-promoted, catalytic method for the regioselective synthesis of allylic acetates from monosubstituted olefins via C-H oxidationQ75399074
Late-stage intermolecular CH activation for lead diversification: a highly chemoselective oxyfunctionalization of the C-9 position of potent bryostatin analoguesQ81212316
Hydrocarbon oxidation vs C-C bond-forming approaches for efficient syntheses of oxygenated moleculesQ81262820
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Expanding the substrate scope for C-H amination reactions: oxidative cyclization of urea and guanidine derivativesQ82763339
A Rh-Catalyzed C-H Insertion Reaction for the Oxidative Conversion of Carbamates to OxazolidinonesQ88522085
P433issue23
P407language of work or nameEnglishQ1860
P921main subjectdiastereoselectivityQ64131393
P304page(s)7274-7276
P577publication date2007-05-22
P1433published inJournal of the American Chemical SocietyQ898902
P1476titlesyn-1,2-Amino alcohols via diastereoselective allylic C-H amination
P478volume129

Reverse relations

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