CHIRAL CALIXARENES DERIVED FROM RESORCINOL .2. FUNCTIONALIZATION BY MANNICH REACTION WITH ALPHA-AMINOALCOHOLS

IWANEK W, WOLFF C, Mattay J (1995)
Tetrahedron Letters 36(49): 8969-8972.

Journal Article | Published | English

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Abstract
A new type of chiral resorc[4]arene is described. The formation of both enantiomers of 4 is controlled by the alpha-aminoalcohols 3 used in the Mannich reaction. Although 1,3-oxazine rings could be formed analogously to the condensation reaction with amines only the formation of 1,3-oxazolidine derivatives is observed.
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IWANEK W, WOLFF C, Mattay J. CHIRAL CALIXARENES DERIVED FROM RESORCINOL .2. FUNCTIONALIZATION BY MANNICH REACTION WITH ALPHA-AMINOALCOHOLS. Tetrahedron Letters. 1995;36(49):8969-8972.
IWANEK, W., WOLFF, C., & Mattay, J. (1995). CHIRAL CALIXARENES DERIVED FROM RESORCINOL .2. FUNCTIONALIZATION BY MANNICH REACTION WITH ALPHA-AMINOALCOHOLS. Tetrahedron Letters, 36(49), 8969-8972.
IWANEK, W., WOLFF, C., and Mattay, J. (1995). CHIRAL CALIXARENES DERIVED FROM RESORCINOL .2. FUNCTIONALIZATION BY MANNICH REACTION WITH ALPHA-AMINOALCOHOLS. Tetrahedron Letters 36, 8969-8972.
IWANEK, W., WOLFF, C., & Mattay, J., 1995. CHIRAL CALIXARENES DERIVED FROM RESORCINOL .2. FUNCTIONALIZATION BY MANNICH REACTION WITH ALPHA-AMINOALCOHOLS. Tetrahedron Letters, 36(49), p 8969-8972.
W. IWANEK, C. WOLFF, and J. Mattay, “CHIRAL CALIXARENES DERIVED FROM RESORCINOL .2. FUNCTIONALIZATION BY MANNICH REACTION WITH ALPHA-AMINOALCOHOLS”, Tetrahedron Letters, vol. 36, 1995, pp. 8969-8972.
IWANEK, W., WOLFF, C., Mattay, J.: CHIRAL CALIXARENES DERIVED FROM RESORCINOL .2. FUNCTIONALIZATION BY MANNICH REACTION WITH ALPHA-AMINOALCOHOLS. Tetrahedron Letters. 36, 8969-8972 (1995).
IWANEK, W, WOLFF, C, and Mattay, Jochen. “CHIRAL CALIXARENES DERIVED FROM RESORCINOL .2. FUNCTIONALIZATION BY MANNICH REACTION WITH ALPHA-AMINOALCOHOLS”. Tetrahedron Letters 36.49 (1995): 8969-8972.
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