Synthesis of Novel Fluoranthene-Based Conformationally Constrained α-Amino Acid Derivatives and Polycyclic Aromatics via the Diels–Alder Reaction
作者:Sambasivarao Kotha、Milind Meshram
DOI:10.1055/s-0033-1341042
日期:——
assembled using the Diels–Alder reaction as a key step. These α-amino acid derivatives are considered as constrained analogues of phenylalanine (Phe) and play an important role in the design and synthesis of bioactive peptides and some fluorescence chemosensor molecules. Moreover, this strategy has been extended to polycyclic aromatics via the Diels–Alder reaction and subsequent aromatization with DDQ. Conformationally
摘要 构象受限的环状α-氨基酸部分已与荧蒽系统融合。氨基茚满羧酸(Aic)和1,2,3,4-四氢异喹啉羧酸(Tic)衍生物是通过烷基化顺序合成的,而氨基四林羧酸(Atc)衍生物是通过Diels-Alder反应组装为关键步骤。这些α-氨基酸衍生物被认为是苯丙氨酸(Phe)的受约束类似物,在生物活性肽和某些荧光化学传感器分子的设计和合成中起着重要作用。此外,该策略已通过Diels-Alder反应以及随后的DDQ芳构化扩展到多环芳烃。 构象受限的环状α-氨基酸部分已与荧蒽系统融合。氨基茚满羧酸(Aic)和1,2,3,4-四氢异喹啉羧酸(Tic)衍生物是通过烷基化顺序合成的,而氨基四林羧酸(Atc)衍生物是通过Diels-Alder反应组装为关键步骤。这些α-氨基酸衍生物被认为是苯丙氨酸(Phe)的受约束类似物,在生物活性肽和某些荧光化学传感器分子的设计和合成中起着重要作用。此外,该策略已通过Di