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Volumn 22, Issue 5-8, 2003, Pages 1545-1548

Nicotinamide adenine dinucleotide a unique compound for theoretical and synthetic model studies: Chirality as source for high stereospecificity

(1)  Buck, H M a  

a NONE   (Netherlands)

Author keywords

Hydride transfer; MO calculations; NADH NAD+ models; Site specificity

Indexed keywords

HYDROGEN; NICOTINAMIDE ADENINE DINUCLEOTIDE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE;

EID: 0141484586     PISSN: 15257770     EISSN: None     Source Type: Journal    
DOI: 10.1081/NCN-120023030     Document Type: Conference Paper
Times cited : (6)

References (9)
  • 2
    • 0000413402 scopus 로고    scopus 로고
    • +. Criticism on the quantum-chemical MO approach
    • +. Criticism on the quantum-chemical MO approach. Recl. Trav. Chim. Pays-Bas 1996, 115, 329.
    • (1996) Recl. Trav. Chim. Pays-Bas. , vol.115 , pp. 329
    • Buck, H.M.1
  • 4
    • 0026076222 scopus 로고
    • NADH model mediated reduction of C=N substrates: Enantio-selective synthesis of D- and L-phenylglycinates
    • Vekemans, J.A.J.M.; Versleijen, J.P.G.; Buck, H.M. NADH model mediated reduction of C=N substrates: enantio-selective synthesis of D- and L-phenylglycinates. Tetrahedron: Asymmetry 1991, 2, 949.
    • (1991) Tetrahedron: Asymmetry , vol.2 , pp. 949
    • Vekemans, J.A.J.M.1    Versleijen, J.P.G.2    Buck, H.M.3
  • 5
    • 0034613358 scopus 로고    scopus 로고
    • +-NAD(P)H models. 90. Stereoselection controlled by electronic effect of a carbonyl group in oxidation of NAD(P)H analog
    • +-NAD(P)H models. 90. Stereoselection controlled by electronic effect of a carbonyl group in oxidation of NAD(P)H analog. J. Org. Chem. 2000, 65, 6381.
    • (2000) J. Org. Chem. , vol.65 , pp. 6381
    • Ohno, A.1    Oda, S.2    Ishikawa, Y.3    Yamazaki, N.4
  • 6
    • 0000939417 scopus 로고    scopus 로고
    • 2Vπ-cyclic mono- and dications with internal cross-linking. A Hückel approach for the description of antiaromaticity
    • 2Vπ-cyclic mono- and dications with internal cross-linking. A Hückel approach for the description of antiaromaticity. Int. J. Quantum Chem. 2000, 78, 179.
    • (2000) Int. J. Quantum Chem. , vol.78 , pp. 179
    • Buck, H.M.1
  • 7
    • 0035151573 scopus 로고    scopus 로고
    • Elementary addition-substitution reactions. Hückel approach for the description of aromatic and antiaromatic arylmethyl cations
    • Buck, H.M. Elementary addition-substitution reactions. Hückel approach for the description of aromatic and antiaromatic arylmethyl cations. Int. J. Quantum Chem. 2001, 81, 66.
    • (2001) Int. J. Quantum Chem. , vol.81 , pp. 66
    • Buck, H.M.1
  • 8
    • 0037022754 scopus 로고    scopus 로고
    • Calculated geometries of dications of his odd-membered π-ring systems containing a NCN fragment and related π-systems. An opposite out-of-plane rotation of the 4n π-ring subsystems
    • Buck, H.M. Calculated geometries of dications of his odd-membered π-ring systems containing a NCN fragment and related π-systems. An opposite out-of-plane rotation of the 4n π-ring subsystems. Int. J. Quantum Chem. 2002, 87, 37.
    • (2002) Int. J. Quantum Chem. , vol.87 , pp. 37
    • Buck, H.M.1
  • 9
    • 37049106152 scopus 로고
    • Regio- and stereo-selective hydride uptake in model systems related to 3-carbamoyl pyridinium compounds
    • De Kok, P.M-.T.; Buck, H.M. Regio- and stereo-selective hydride uptake in model systems related to 3-carbamoyl pyridinium compounds. J. Chem. Soc., Chem. Commun. 1985, 1009.
    • (1985) J. Chem. Soc., Chem. Commun. , pp. 1009
    • De Kok, P.M.-T.1    Buck, H.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.