287205-66-7Relevant academic research and scientific papers
Asymmetric N-sulfinyl dienophile Diels-Alder cycloadditions using chiral T1(IV)-based Lewis acids
Bayer, Annette,Gautun, Odd R.
, p. 3743 - 3746 (2000)
Enantioselective Diels-Alder reactions of 1,3-cyclohexadiene with N- sulfinylbenzyl carbamate (1a) or N-sulfinyl-p-toluenesulfonamide (1b) promoted by chiral Ti(IV)-based Lewis acids are reported. The endo-adducts were obtained in 15-76% ee. (C) 2000 Elsevier Science Ltd.
