144543-35-1Relevant articles and documents
Synthesis of highly substituted symmetrical 1,3-dienes via organocuprate oxidation
Aves, Sarah. J.,O'Connell, Kieron M. G.,Pike, Kurt G.,Spring, David R.
, p. 298 - 300 (2012)
Oxidation of alkenyl organocuprates formed from alkenyl halides allows the formation of highly substituted symmetrical 1,3-dienes. Cuprates formed from organolithiums and Grignard reagents can be tolerated and the reaction proceeds with retention of alkenyl geometry. Georg Thieme Verlag Stuttgart New York.
A new ground state single electron donor for excess electron transfer studies in DNA
Trindler, Christian,Manetto, Antonio,Eirich, Juergen,Carell, Thomas
supporting information; experimental part, p. 3583 - 3584 (2009/12/03)
A new photoinducible single electron donor has been developed, which, when linked to thymidine, is shown to be an efficient ground state reducing agent in DNA; the donor can be activated at wavelengths where standard DNA does not absorb.
Studies on the thermal generation and reactivity of a class of (σ,π)-1,4-biradicals
Myers, Andrew G.,Dragovich, Peter S.,Kuo, Elaine Y.
, p. 9369 - 9386 (2007/10/02)
(Z)-1,2,4-Heptatrien-6-yne and compounds that contain the (Z)-allene-ene-yne functional group or that form it in a serial reaction sequence were prepared and shown to undergo a mild thermal reaction to form aromatic products. All observations suggest that
