Hydrogen bonding chains and rings structural motifs in new series of N-phthaloyl aminocarboxylic acid derivatives. Solid state microwave synthesis, structural …

…, HMA Al-Hazimi, A El-Faham, J Reedijk

Index: Al-Farhan, Khalid; Ghazzali, Mohamed; Al-Hazimi, Hassan M.A.; El-Faham, Ayman; Reedijk, Jan Journal of Molecular Structure, 2011 , vol. 994, # 1-3 p. 269 - 275

Full Text: HTML

Citation Number: 3

Abstract

Abstract A series of six N-phthaloyl aminocarboxylic acids were synthesized by using improved microwave irradiation with a multimode reactor. X-ray single crystal diffraction established the molecular structure of three N-protected aminocarboxylic acids derivatives, and spectral data agree with these in solution. The hydrogen bonding characteristics of this class of molecules are discussed on the basis of crystal structural analyses, MP2/DFT ...

Related Articles:

Highly efficient stereoconservative amidation and deamidation of α-amino acids

[Shendage, Deepak M.; Froehlich, Roland; Haufe, Guenter Organic Letters, 2004 , vol. 6, # 21 p. 3675 - 3678]

Nucleophilic Reactivities of Imide and Amide Anions

[Kubo, Akira; Kubota, Hitoshi; Takahashi, Masami; Nunami, Ken-Ichi Tetrahedron Letters, 1996 , vol. 37, # 28 p. 4957 - 4960]

Nucleophilic Reactivities of Imide and Amide Anions

[Kubo, Akira; Kubota, Hitoshi; Takahashi, Masami; Nunami, Ken-Ichi Tetrahedron Letters, 1996 , vol. 37, # 28 p. 4957 - 4960]

Nucleophilic Reactivities of Imide and Amide Anions

[Kubo, Akira; Kubota, Hitoshi; Takahashi, Masami; Nunami, Ken-Ichi Tetrahedron Letters, 1996 , vol. 37, # 28 p. 4957 - 4960]

More Articles...