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Volumn 43, Issue 47, 2002, Pages 8515-8518

Diastereoselective synthesis of 1,2,3,6-tetrahydrophosphinine 1-oxides with an exocyclic P-function by a Michael type addition

Author keywords

Conformation; Michael reactions; Phosphorus heterocycles; Stereoselection

Indexed keywords

ANION; OXIDE; PHOSPHINE DERIVATIVE; PHOSPHITE; PHOSPHORUS DERIVATIVE;

EID: 0037131734     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)02081-6     Document Type: Article
Times cited : (36)

References (12)
  • 1
    • 84944077811 scopus 로고    scopus 로고
    • Six-membered rings with one phosphorus atom
    • Katritzky, A. R; Rees, C. W.; Scriven, E. F. V., Eds.; Pergamon: Oxford, Ch. 12
    • Hewitt, D. G. Six-membered rings with one phosphorus atom. In Comprehensive Heterocyclic Chemistry II; Katritzky, A. R; Rees, C. W.; Scriven, E. F. V., Eds.; Pergamon: Oxford, 1996; Vol. 5, Ch. 12.
    • (1996) Comprehensive Heterocyclic Chemistry II , vol.5
    • Hewitt, D.G.1
  • 6
    • 0005179149 scopus 로고    scopus 로고
    • note
    • 3 solution.
  • 7
    • 0005125916 scopus 로고    scopus 로고
    • Quantum chemical calculations were carried out using the Gaussian98 program package. Geometries of the different conformers of 2a and 3b were optimised at the B3LYP/3-21G* level of theory. Relative energies were calculated with B3LYP/6-31+G* single point calculations. In the case of 3b, further refinement of the geometries at this level of theory did not change the relative energies of the different conformers significantly
    • Quantum chemical calculations were carried out using the Gaussian98 program package. Geometries of the different conformers of 2a and 3b were optimised at the B3LYP/3-21G* level of theory. Relative energies were calculated with B3LYP/6-31+G* single point calculations. In the case of 3b, further refinement of the geometries at this level of theory did not change the relative energies of the different conformers significantly.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.