Tetrahedron Letters p. 1681 - 1684 (1997)
Update date:2022-09-26
Topics:
Burgess, Kevin
Li, Shiming
Rebenspies, Joe
Optically active samples of the N-protected 1,3-cyclobutane amino acids 1 and 2 were prepared from α-pinene. The synthesis of 1 is enantiodivergent insofar as both optical antipodes of the product can be prepared from the same α-pinene enantiomer. Single crystal X-ray diffraction studies of derivatives of 1 reveal these compounds can have extended conformations.
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Doi:10.1016/S0957-4166(97)00151-1
(1997)Doi:10.1002/(SICI)1522-2675(20000510)83:5<855::AID-HLCA855>3.0.CO;2-9
(2000)Doi:10.1016/j.chempr.2019.03.008
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(1997)Doi:10.1039/a703063k
(1997)Doi:10.1080/01615440209604133
(1939)
