+++SD + ACS + Chemistry Letters, EJOCh = 9 статей

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1) Synthesis and antiviral evaluation of [(2′S, 3′S)-bis(hydroxymethyl)azeitidin-1-yl]pyrimidine nucleosides: analogs of oxetanocin-A
Fumio Hosono, Shigeru Nishiyama and Shosuke Yamamura, Takao Izawa and Kuniki Kato
Bioorganic & Medicinal Chemistry Letters
Volume 4, Issue 17, 8 September 1994, Pages 2083-2086

Код: Выделить всё

http://dx.doi.org/10.1016/S0960-894X(01)80106-2

2) A Convenient Method for the Preparation of 3-Azetidinylidene Acetic Acid
Marc Vuilhorgne, Alain Commerçon and Serge Mignani
Chemistry Letters
Vol. 28 (1999), No. 7 p.605

Код: Выделить всё

http://dx.doi.org/10.1246/cl.1999.605

3) 2-Aryl-N-tosylazetidines as Formal 1,4-Dipoles for [4 + 2] Cycloaddition Reactions with Nitriles: An Easy Access to the Tetrahydropyrimidine Derivatives
B. A. Bhanu Prasad, Alakesh Bisai, and Vinod K. Singh
Org Lett 2004, 6(26), pp 4829–4831

Код: Выделить всё

http://dx.doi.org/10.1021/ol048161l

4) Asymmetric Synthesis of 2-Mono- and 2,3-trans-Disubstituted Azetidines
Dieter Enders, Jörg Gries, Zin-Sig Kim
European Journal of Organic Chemistry 2004, 21, p 4471-4482.

Код: Выделить всё

http://dx.doi.org/10.1002/ejoc.200400473

5) A Concise Synthesis of a Novel Insulin-Like Growth Factor I Receptor (IGF-IR) Inhibitor
Joel Slade, Joginder Bajwa, Hui Liu, David Parker, James Vivelo, Guang-Pei Chen, John Calienni, Edwin Villhauer, Kapa Prasad*, Oljan Repi and Thomas J. Blacklock
Organic Process Research and Development 2007, 11(5), pp 825–835

Код: Выделить всё

http://dx.doi.org/10.1021/op700052u

6) Azetidine Based Transition State Analogue Inhibitors of N-Ribosyl Hydrolases and Phosphorylases
Gary B. Evans, Richard H. Furneaux, Ben Greatrex, Andrew S. Murkin, Vern L. Schramm and Peter C. Tyler
Journal of Medicinal Chemistry 2008, Volume 51, Issue 4, pp 948–956

Код: Выделить всё

http://dx.doi.org/10.1021/jm701265n

7) A One-Pot Preparation of 1,3-Disubstituted Azetidines
Michael C. Hillier and Cheng-yi Chen
JOCh. – 2006, 71(20), pp 7885–7887

Код: Выделить всё

http://dx.doi.org/10.1021/jo061147x

Synthesis of 3-Fluoroazetidines
Willem Van Brabandt, Guido Verniest, Dirk De Smaele, Guillaume Duvey, and Norbert De Kimpe
JOCh. – 2006, 71(18), pp 7100–7102

Код: Выделить всё

http://dx.doi.org/10.1021/jo061095b

9) N,N‘-Carbonyldiimidazole-Mediated Cyclization of Amino Alcohols to Substituted Azetidines and Other N-Heterocycles
Renata Marcia de Figueiredo, Roland Fröhlich, and Mathias Christmann
JOCh. – 2006, 71(11), pp 4147–4154

Код: Выделить всё

http://dx.doi.org/10.1021/jo060130b

СПАСИБО!!!

[Arminum]

Статьи 3, 5-9

[Arminum]

Нет 1, 2 и 4 (в смысле у меня доступа к ним нет)

[Anhydride]

Спасибо!!

[Myrsten]

4

[Demcha]

1,2 +++