Chiral 1,3-cyclobutane amino acids: Syntheses and extended conformations Academic Article

abstract

• Optically active samples of the N-protected 1,3-cyclobutane amino acids 1 and 2 were prepared from -pinene. The synthesis of 1 is enantiodivergent insofar as both optical antipodes of the product can be prepared from the same -pinene enantiomer. Single crystal X-ray diffraction studies of derivatives of 1 reveal these compounds can have extended conformations.

authors

• Burgess, Kevin

published proceedings

• TETRAHEDRON LETTERS

altmetric score

• 3

author list (cited authors)

• Burgess, K., Li, S. M., & Rebenspies, J.

citation count

• 31

complete list of authors

• Burgess, K||Li, SM||Rebenspies, J

publication date

• March 1997

publisher

• Elsevier  Publisher

keywords

• Amino Acid
• Conformationally Constrained
• Cyclobutane

Digital Object Identifier (DOI)

• 10.1016/S0040-4039(97)00200-1

start page

• 1681

end page

• 1684

volume

• 38

issue

• 10

URL

• http://dx.doi.org/10.1016/s0040-4039(97)00200-1