+++Org. Lett. 2010 часть 1

[Liverpool]

Помогите, пожалуйста, кто может:

1) Stereochemical and Skeletal Diversity Arising from Amino Propargylic Alcohols
Daniela Pizzirani, Taner Kaya, Paul A. Clemons and Stuart L. Schreiber
Org. Lett. 2010, 12 (12), pp 2822–2825

Код: Выделить всё

http://dx.doi.org/10.1021/ol100914b

2) Allenamide Hydro−Hydroxyalkylation: 1,2-Amino Alcohols via Ruthenium-Catalyzed Carbonyl anti-Aminoallylation
Jason R. Zbieg, Emma L. McInturff and Michael J. Krische
Org. Lett. 2010, 12 (11), pp 2514–2516

Код: Выделить всё

http://dx.doi.org/10.1021/ol1007235

3) A Formal [4 + 4] Complementary Ambiphile Pairing Reaction: A New Cyclization Pathway for ortho-Quinone Methides
Thiwanka B. Samarakoon, Moon Y. Hur, Ryan D. Kurtz and Paul R. Hanson
Org. Lett. 2010, 12 (10), pp 2182–2185

Код: Выделить всё

http://dx.doi.org/10.1021/ol100495w

4) Pd-Catalyzed Carboamination of Oxazolidin-2-ones: A Stereoselective Route to trans-2,5-Disubstituted Pyrrolidines
Georgia S. Lemen and John P. Wolfe
Org. Lett. 2010, 12 (10), pp 2322–2325

Код: Выделить всё

http://dx.doi.org/10.1021/ol1006828

5) Decoding Stereocontrol During the Photooxygenation of Oxazolidinone-Functionalized Enecarbamates
Marissa R. Solomon, J. Sivaguru, Steffen Jockusch, Waldemar Adam and Nicholas J. Turro
Org. Lett. 2010, 12 (9), pp 2142–2145

Код: Выделить всё

http://dx.doi.org/10.1021/ol100174r

6) α-Amino-β-hydroxy-γ-lactam for Constraining Peptide Ser and Thr Residue Conformation
Daniel J. St-Cyr, Andrew G. Jamieson and William D. Lubell
Org. Lett. 2010, 12 (8), pp 1652–1655

Код: Выделить всё

http://dx.doi.org/10.1021/ol1000582

7) Salicylaldehyde Ester-Induced Chemoselective Peptide Ligations: Enabling Generation of Natural Peptidic Linkages at the Serine/Threonine Sites
Xuechen Li, Hiu Yung Lam, Yinfeng Zhang and Chun Kei Chan
Org. Lett. 2010, 12 (8), pp 1724–1727

Код: Выделить всё

http://dx.doi.org/10.1021/ol1003109

8 ) Acortatarins A and B, Two Novel Antioxidative Spiroalkaloids with a Naturally Unusual Morpholine Motif from Acorus tatarinowii
Xiao-Gang Tong, Li-Li Zhou, Yue-Hu Wang, Chengfeng Xia, Ye Wang, Min Liang, Fan-Fan Hou and Yong-Xian Cheng
Org. Lett. 2010, 12 (8), pp 1844–1847

Код: Выделить всё

http://dx.doi.org/10.1021/ol100451p

9) Formal [4+3] Epoxide Cascade Reaction via a Complementary Ambiphilic Pairing Strategy
Alan Rolfe, Thiwanka B. Samarakoon and Paul R. Hanson
Org. Lett. 2010, 12 (6), pp 1216–1219

Код: Выделить всё

http://dx.doi.org/10.1021/ol100035e

10) Diastereoselective Allylstannane Additions to (S)-5,6-Dihydro-2H-5-phenyloxazin-2-one. A Concise Synthesis of (S)-β-Methylisoleucine
Julie A. Pigza and Tadeusz F. Molinski
Org. Lett. 2010, 12 (6), pp 1256–1259

Код: Выделить всё

http://dx.doi.org/10.1021/ol1001126

Большое спасибо!

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