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Chemistry - A European Journal

Volumn 14, Issue 29, 2008, Pages 8956-8963

Stereoselective synthesis of 4-dehydroxydiversonol employing enantioselective palladium-catalysed domino reactions

(6) Tietze, Lutz F a Spiegl, Dirk A a Stecker, Florian a Major, Julia a Raith, Christian a Große, Christian a

a UNIVERSITY OF GÖTTINGEN (Germany)

Author keywords

Asymmetric catalysis; Domino reactions; Palladium; Tetrahydroxanthenones; Wacker oxidation

Indexed keywords

CARBON MONOXIDE; CARBONYLATION; CHEMICAL OXYGEN DEMAND; METHANOL; OXIDATION; PALLADIUM; PALLADIUM COMPOUNDS; REACTION KINETICS; STEREOCHEMISTRY; STEREOSELECTIVITY;

ASYMMETRIC CATALYSIS; BENZYLIC; BINAPHTHYL; CARBONYLATION REACTIONS; CRYSTAL STRUCTURE ANALYSES; DOMINO PROCESSES; DOMINO REACTIONS; DOUBLE BONDS; ENANTIOSELECTIVE; METHYL ACRYLATES; METHYLENE GROUPS; RELATIVE CONFIGURATIONS; STARTING MATERIALS; STEREOSELECTIVE SYNTHESIS; SYNTHESIS OF; TETRAHYDROXANTHENONES; TRIFLUOROACETATE; WACKER OXIDATION;

CRYSTAL STRUCTURE;

AMINE; DIVERSONOL; PALLADIUM; XANTHONE DERIVATIVE;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; HYDROXYLATION; STEREOISOMERISM; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

AMINES; CATALYSIS; CRYSTALLOGRAPHY, X-RAY; HYDROXYLATION; MODELS, MOLECULAR; MOLECULAR STRUCTURE; PALLADIUM; STEREOISOMERISM; XANTHONES;

EID: 55049089902 PISSN: 09476539 EISSN: 15213765 Source Type: Journal
DOI: 10.1002/chem.200800967 Document Type: Article

Times cited : (65)

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- Crystal data for 4: C15H18O5; M=278.29; triclinic; P1; a, 11.119(2, b, 15.605(3, c= 16.530(3) Å; α, 107.90(3, β= 92.35(3, γ, 97.07(3)°; V=2699.1 (9) Å3; Z, 8; T=100(2) K; 40706 reflections measured (colourless blocks, 2.82 < 0 < 60.34°, 7856 unique reflections (Aiu1 =0.0453, 775 parameters. Data were collected on a Bruker three-cycle diffractometer with a SMART 6000 detector and CuKα radiation (λ=1.54178 Å) at low temperature. The structure was solved by direct methods and refined by full-matrix leastsquares procedures against F2 with SHELX (ref, 22, Non-hydrogen atoms were refined anisotropically, hydrogen atoms in CH, groups were added by using the riding model. R1 F04σF0, 0.0519, wR2, 0.1345, GooF= 1.130. CCDC-686256 contains the supplementary crystallo
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