+++Synthesis СПАСИБО

[Люсёнок]

И вновь я!
1. Reetz, Manfred T.; Oka, Hiromasa; Goddard,Richard; Binaphthyldiamine-Based Diazaphospholidinesas a New Class of Chiral Monodentate¬ P-Ligands; Synthesis; English; 12; 2003; 1809 - 1814;

Код: Выделить всё

http://dx.doi.org/10.1055/s-2003-41036

2. Tracey, Michael R.; Hsung, Richard P.;Lambeth, Robert H.; Allylated β-Ketoesters as Precursors in Paal-Knorr-Type Pyrrole Synthesis: Preparations of Chiral and Bispyrroles; Synthesis; English; 6; 2004; 918 -922;

Код: Выделить всё

http://dx.doi.org/10.1055/s-2004-815976

3. Ma, Guang-Ning; Zhang, Yun-Peng; Shi, Min; L-Proline Diamides with an Axially Chiral Binaphthylene Backbone as Efficient¬ Organocatalysts for Direct Asymmetric Aldol Reactions: The Effect of Acetic Acid; Synthesis; English; 2; 2007; 197 - 208;

Код: Выделить всё

http://dx.doi.org/10.1055/s-2006-958924

4. Caronna, Tullio; Fontana, Francesca; Mele, Andrea; Sora, Isabella Natali; Panzeri, Walter; Vigano, Luca; A Simple Approach for the Synthesis of 7,8-Diaza[5]helicene; Synthesis; English; 3; 2008; 413 - 416;

Код: Выделить всё

http://dx.doi.org/10.1055/s-2008-1032021

5. Zhang, Tao; Liu, Sijia; Shi, Min; Zhao, Meixin; N-Heterocyclic Carbene-Acetylamide Palladium Complexes and Their Catalytic Activities in Heck-Mizoroki Reactions; Synthesis; English; 17; 2008; 2819 - 2824;

Код: Выделить всё

http://dx.doi.org/10.1055/s-2008-1067199

[macro]

1,3-5

[Demcha]

2 +++