+++Осталась #7 из Current Organic Chemistry

[OrganicChemist]

Уважаемые коллеги, помогите, пожалуйста, скачать статьи:

1. Total Synthesis and Biological Evaluation of Monorhizopodin and 16-epi-Monorhizopodin

Prof. Dr. K. C. Nicolaou Dr. Xuefeng Jiang Dr. Peter J. Lindsay-Scott, Dr. Andrei Corbu, Dr. Sawako Yamashiro,
Dr. Andrea Bacconi and Prof. Dr. Velia M. Fowler

Angewandte Chemie International Edition
Volume 50, Issue 5, pages 1139–1144, February 1, 2011

DOI:

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 http://dx.doi.org/10.1002/anie.201006780  

2. Synthesis of the macrolactone structure of the aurisides

Emmanuel Bourceta, Fabienne Fachea, Olivier Piva

Tetrahedron
Volume 66, Issue 6, 6 February 2010, Pages 1319–1326

DOI:

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 http://dx.doi.org/10.1016/j.tet.2009.12.008  

3. Stereocontrolled Synthesis of the Highly Functionalized Core Structure of Aurisides by Ring-Closing Metathesis

Emmanuel Bourcet, Fabienne Fache and Olivier Piva

European Journal of Organic Chemistry
Volume 2010, Issue 21, pages 4075–4087, July 2010

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 http://dx.doi.org/10.1002/ejoc.201000331  

4. Atom-Economic and Stereoselective Syntheses of the Ring A and B Subunits of the Bryostatins

Prof. Barry M. Trost, Dr. Hanbiao Yang, Dr. Cheyenne S. Brindle and Dr. Guangbin Dong

Chemistry - A European Journal
Volume 17, Issue 35, pages 9777–9788, August 22, 2011

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 http://dx.doi.org/10.1002/chem.201002930  

5. A Ru-Catalyzed Tandem Alkyne−Enone Coupling/Michael Addition:  Synthesis of 4-Methylene-2,6-cis-tetrahydropyrans

Barry M. Trost, Hanbiao Yang , and Georg Wuitschik

Org. Lett., 2005, 7 (21), pp 4761–4764

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 http://dx.doi.org/10.1021/ol0520065  

6. Asymmetric Total Synthesis of the Epothilone Sagopilone – From Research to Development

Ulrich Klar, Johannes Platzek

Synlett 2012; 23(9): 1291-1299

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 http://dx.doi.org/10.1055/s-0031-1290163  

7. Recent Developments in the Stereocontrolled Synthesis of Highly Substituted Cyclopentane Core Structures: From Drug Discovery Research to Natural Product Synthesis

Brian Heasley

Current Organic Chemistry 2014; 18(6): 641-686

DOI:

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 http://dx.doi.org/10.2174/13852728113176660150  

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