Royal Society of Chemistry, Chemical Communications, 39(49), p. 4361-4363, 2013
DOI: 10.1039/c2cc37102b
Wiley-VCH Verlag, ChemInform, 37(44), p. no-no, 2013
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An efficient organocatalyzed strategy for the synthesis of 3-amino-1-indanols has been developed. This method is complementary to the conventional Friedel-Crafts strategy. It is also applicable to the synthesis of enantioenriched 3-amino-1-indanols.