Conformationally restricted amino acids: Diastereoselective substitution at the β-position of L-tryptophan

DOI: 10.1016/S0040-4039(00)60945-0

Source and publish data:

Tetrahedron Letters p. 6251 - 6254 (1992)

Update date:2022-08-04

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Authors:

Bruncko, Milan

Crich, David

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Article abstract of DOI:10.1016/S0040-4039(00)60945-0

Higher order cuprates add with extreme exo-facial selectivity to the chiral tetrahydropyrroloindole 3, itself prepared in enantiomerically pure form from L-tryptophan: treatment of the adducts with trifluoroacetic acid provides diastereo- and enantiomeric

Full text of DOI:10.1016/S0040-4039(00)60945-0

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Product name:erythro-N-(Methoxycarbonyl)-β-phenyl-L-tryptophan methyl ester

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