Synthesis of chiral phosphetanes

Tetrahedron Letters

Volumn 38, Issue 17, 1997, Pages 2947-2950

  Marinetti, Angela ^a   Kruger, Virginie ^a   Buzin, François Xavier ^a  

^a LABORATOIRE HÉTÉROÉLÉMENTS ET COORDINATION   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ORGANOPHOSPHORUS COMPOUND;

ARTICLE; CHIRALITY; DRUG SYNTHESIS; IN VITRO STUDY; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0030972372     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)00508-X     Document Type: Article

References (27)

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15. C-P = 41.1 Hz).
16. 3).
17. Niediek, K.; Neumüller, B. Z. Anorg. Allg. Chem. 1993, 619, 885-888.
18. The cyclic sulfates of the 1,3-propanediols have been prepared according to the Sharpless procedure: Gao, Y.; Sharpless, K.B.; J. Am. Chem. Soc., 1988, 110, 7538-7539.
19. 3).
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21. 3).
22. 2).
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25. To date, only P-menthyl-substituted, monodentate phosphetanes have been considered for their use in asymmetric catalysis: (a) Marinetti, A. Tetrahedron Lett. 1994, 35, 5861-5864.
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27. (c) Marinetti, A.; Kruger, V.; Ricard, L. J. Organomet. Chem. 1997, in press.