Помогите, кто чем может !
1. Keith R. Adams, Raymond Bonnett, Philip J. Burke, Antonio Salgado and Maria Asunción Vallés
J. Chem. Soc., Chem. Commun., 1993, 1860 - 1861
The 2,3-secochlorin-2,3-dione system
Код: Выделить всё
http://dx.doi.org/10.1039/C39930001860J. Chem. Soc., Perkin Trans. 1, 1997, 1769 - 1772
Cleavage of (octaethyl-2,3-dihydroxychlorinato)nickel(II) to give the novel 2,3-dioxo-2,3-secochlorin system
Код: Выделить всё
http://dx.doi.org/10.1039/a701152kJ. Chem. Soc., Chem. Commun., 1989, 1822 - 1823
Second generation tumour photosensitisers: the synthesis of octa-alkyl chlorins and bacteriochlorins with graded amphiphilic character
Код: Выделить всё
http://dx.doi.org/10.1039/C39890001822Tetrahedron Letters 1996 Vol. 37, Iss.22. P. 3781-3784
Effect of substituents in OsO4 reactions of metallochlorins regioselective synthesis of isobacteriochlorins and bacteriochlorins
Код: Выделить всё
http://dx.doi.org/10.1016/0040-4039(96)00712-55.Christian Brückner and David Dolphin
Tetrahedron Letters 1995 Vol.36, Iss.52, P. 9425-9428
β,β '-dihydroxylation of meso-tetraphenylchlorins and metallochlorins
Код: Выделить всё
http://dx.doi.org/10.1016/0040-4039(95)02052-76. Christian Brückner and David Dolphin
Tetrahedron Letters 1995 Vol.36, Iss.19,P. 3295-3298
2,3-vic-Dihydroxy-meso-tetraphenylchlorins from the osmium tetroxide oxidation of meso-tetraphenylporphyrin
Код: Выделить всё
http://dx.doi.org/10.1016/0040-4039(95)00524-G