Highly enantioenriched 5-pyrimidyl alkanols I and II was formed using tetrathia-[7]-helicenes as a chiral initiator in the enantioselective addn. of diisopropylzinc to pyrimidine-5-carbaldehyde, in conjunction with asym. autocatalysis
Enantioselective synthesis induced by tetrathia-[7]-helicenes in conjunction with asymmetric autocatalysis / T. Kawasaki, K. Suzuki, E. Licandro, A. Bossi, S. Maiorana, K. Soai. - In: TETRAHEDRON-ASYMMETRY. - ISSN 0957-4166. - 17:14(2006), pp. 2050-2053. [10.1016/j.tetasy.2006.07.015]
Enantioselective synthesis induced by tetrathia-[7]-helicenes in conjunction with asymmetric autocatalysis
E. Licandro;A. Bossi;S. Maiorana;
2006
Abstract
Highly enantioenriched 5-pyrimidyl alkanols I and II was formed using tetrathia-[7]-helicenes as a chiral initiator in the enantioselective addn. of diisopropylzinc to pyrimidine-5-carbaldehyde, in conjunction with asym. autocatalysis
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