The aza-Diels–Alder reaction protocol—a useful approach to chiral, sterically constrained α-amino acid derivatives
摘要:
Different types of polycyclic alpha -amino acid derivatives are prepared from chiral imines by using well-established aza-Diels-Alder reaction conditions. Simply by varying the diene moiety, different products such as spirocyclic compounds 8 and 9, anthracene 10, and tetrahydroquinolines 15-21 are formed. (C) 2001 Elsevier Science Ltd. All rights reserved.
The aza-Diels–Alder reaction protocol—a useful approach to chiral, sterically constrained α-amino acid derivatives
摘要:
Different types of polycyclic alpha -amino acid derivatives are prepared from chiral imines by using well-established aza-Diels-Alder reaction conditions. Simply by varying the diene moiety, different products such as spirocyclic compounds 8 and 9, anthracene 10, and tetrahydroquinolines 15-21 are formed. (C) 2001 Elsevier Science Ltd. All rights reserved.
The aza-Diels–Alder reaction protocol—a useful approach to chiral, sterically constrained α-amino acid derivatives
作者:Sophie K Bertilsson、Jenny K Ekegren、Stefan A Modin、Pher G Andersson
DOI:10.1016/s0040-4020(01)00531-2
日期:2001.7
Different types of polycyclic alpha -amino acid derivatives are prepared from chiral imines by using well-established aza-Diels-Alder reaction conditions. Simply by varying the diene moiety, different products such as spirocyclic compounds 8 and 9, anthracene 10, and tetrahydroquinolines 15-21 are formed. (C) 2001 Elsevier Science Ltd. All rights reserved.