Stereoselective Synthesis of P-Chiral Phosphorus Compounds from <i>N-tert</i>-Butoxycarbonyl Amino Acids
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Reaction of the N-t-Boc amino acids alanine and valine with PhPCl2 gives the P-chiral trans-1,3,2-oxazaphospholidinones exclusively. Variable-temperature NMR and examination of the glycine derivative shows that the isomers observed are due to t-Boc rotation.
N-叔丁氧羰基(N-t-Boc)氨基酸丙氨酸与缬氨酸与苯基二氯化膦(PhPCl2)发生反应,可专一性生成P-手性反式-1,3,2-氧杂磷杂环戊酮类化合物。借助变温核磁共振(Variable-temperature NMR)技术并对该甘氨酸衍生物开展考察,结果显示所观测到的异构体均源于叔丁氧羰基(t-Boc)的旋转。
创建时间:
2016-05-06



