Complete and unambiguous assignments of 1H and 13C chemical shifts of new arylamino derivatives of ortho-naphthofuranquinones

Magn Reson Chem. 2008 Dec;46(12):1158-62. doi: 10.1002/mrc.2250.

Abstract

Six new nor-beta-lapachones have been synthesized from reaction of 3-bromo-nor-beta-lapachone with arylamines. These derivatives have potent anticancer properties against several cell lines. Here, we report complete unambiguous assignments of (1)H and (13)C chemical shifts of the new compounds. The assignments were made using a combination of one- and two-dimensional NMR techniques ((1)H, (13)C, (1)H-(1)H COSY, (1)H-(13)C HSQC, and (1)H-(13)C HMBC).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amines / chemistry
  • Antineoplastic Agents / chemistry
  • Carbon Isotopes
  • Furans / chemistry
  • Magnetic Resonance Spectroscopy / methods*
  • Naphthalenes / chemistry
  • Quinones / chemistry*

Substances

  • Amines
  • Antineoplastic Agents
  • Carbon Isotopes
  • Furans
  • Naphthalenes
  • Quinones