593284-22-1Relevant academic research and scientific papers
Novel NMR chiral solvating agents derived from (1R,2R)-diaminocyclohexane: synthesis and enantiodiscrimination for chiral carboxylic acids
Yang, Xuemei,Wang, Guitao,Zhong, Cheng,Wu, Xiaojun,Fu, Enqin
, p. 916 - 921 (2006)
A series of new compounds, (1R,2R)-1-(1′,8′-naphthalimide)-2-aminocyclohexane 1 and its 4′-derivatives 2 and 3 derived from (1R,2R)-1,2-diaminocyclohexane have been synthesized conveniently and efficiently. 1H NMR spectroscopy was employed to i
A highly efficient large-scale asymmetric direct intermolecular aldol reaction employing L-prolinamide as a recoverable catalyst
Yang, Yang,He, Yan-Hong,Guan, Zhi,Huang, Wei-Da
supporting information; scheme or table, p. 2579 - 2587 (2010/12/25)
A new, simple bifunctional, recoverable and reusable L-prolinamide organocatalyst that promotes aldol reactions while achieving a respectable level of enantioselectivity is reported. This organocatalyst is applicable to the reactions of a wide range of ar
Facile monoprotection of trans-1,2-diaminocyclohexane
Kaik,Gawronski
, p. 1559 - 1563 (2007/10/03)
A new method of monoprotection of C2-symmetric trans-1,2-diaminocyclohexane as the N-phthaloyl, N-tetrachlorophthaloyl or N-1,8-naphthaloyl derivative is presented. The first two derivatives are obtained with high yields and can be readily transformed into other unsymmetrical derivatives of trans-1,2-diaminocyclohexane.
