. "Highly Enantioselective Aza-Baylis-Hillman-Type Reaction of alpha,beta-Unsaturated Aldehydes with In Situ Generated N-Boc- and N-Cbz-Imines"@en . "Enantioselective; Aza-Baylis-Hillman-Type Reaction; alpha,beta-Unsaturated Aldehydes; N-Boc- and N-Cbz-Imines"@en . . "\u010C\u00EDhalov\u00E1, Sylva" . "RIV/00216208:11310/09:10000619" . "DE - Spolkov\u00E1 republika N\u011Bmecko" . . . "Vesel\u00FD, Jan" . . "Highly Enantioselective Aza-Baylis-Hillman-Type Reaction of alpha,beta-Unsaturated Aldehydes with In Situ Generated N-Boc- and N-Cbz-Imines" . "4"^^ . "317154" . "1434-193X" . "4"^^ . . . "Highly Enantioselective Aza-Baylis-Hillman-Type Reaction of alpha,beta-Unsaturated Aldehydes with In Situ Generated N-Boc- and N-Cbz-Imines" . "Reme\u0161, Marek" . "An organocatalytic highly enantioselective aza-Baylis-Hillman reaction of alpha,beta-unsaturated aldehydes with in situ generated N-Boc- and N-Cbz-imines is presented. This novel process opens the pathway for the synthesis of beta-amino carbonyl compounds bearing an alpha-alkylidene group under mild and simple conditions."@en . . "An organocatalytic highly enantioselective aza-Baylis-Hillman reaction of alpha,beta-unsaturated aldehydes with in situ generated N-Boc- and N-Cbz-imines is presented. This novel process opens the pathway for the synthesis of beta-amino carbonyl compounds bearing an alpha-alkylidene group under mild and simple conditions." . "P(GP203/09/P193), Z(MSM0021620857)" . . "[48CEF93D2D9A]" . . "11310" . "36" . . . . . . . "Highly Enantioselective Aza-Baylis-Hillman-Type Reaction of alpha,beta-Unsaturated Aldehydes with In Situ Generated N-Boc- and N-Cbz-Imines"@en . . . . "000273187700002" . . "EUROPEAN JOURNAL OF ORGANIC CHEMISTRY" . "C\u00EDsa\u0159ov\u00E1, Ivana" . "RIV/00216208:11310/09:10000619!RIV10-GA0-11310___" . . "4"^^ . . "Neuveden" .