+++EurJOC, Tetrahedron Lett, Synthesis

[egatsak]

Прошу помочь с поиском пяти статей.

1)

DOI:

http://dx.doi.org/10.1002/ejoc.200600481

Eur J of Organic Chemistry
Volume 2006, Issue 22, pages 5069–5075, November 2006
Transformation of Esters into 2-Substituted Allyl Halides via Tertiary Cyclopropanols: Application in the Stereoselective Synthesis of (2S,3S,7S)-3,7-Dimethyl-2-pentadecyl Acetate, the Sex Pheromone of the Pine Sawfly Neodiprion sertifer
Andrei V. Bekish, Konstantin N. Prokhorevich, Oleg G. Kulinkovich

2)

DOI:

http://dx.doi.org/10.1016/j.tetlet.2004.05.022

Tetrahedron Letters
Volume 45, Issue 27, 28 June 2004, Pages 5253-5255
Transformation of esters into allyl halides via substituted cyclopropanols. Application in the synthesis of (2S,3R,7R/S)-3,7-dimethyltridec-2-yl acetate and propionate, sex attractants of pine sawfly Diprion pini
Andrey V. Bekish, Konstantin N. Prokhorevich, Oleg G. Kulinkovich

3)

DOI:

http://dx.doi.org/10.1016/j.tetlet.2005.08.076

Tetrahedron Letters
Volume 46, Issue 41, 10 October 2005, Pages 6975-6978
Differentiation between the ethoxycarbonyl groups in diethyl malate via their titanium-catalyzed reductive cyclopropanation with ethylmagnesium bromide and subsequent site-selective three-carbon ring cleavage
Andrei V. Bekish, Oleg G. Kulinkovich

4)

DOI:

http://dx.doi.org/10.1016/j.tetlet.2005.08.075

Tetrahedron Letters
Volume 46, Issue 41, 10 October 2005, Pages 6979-6981
A cyclopropanol approach to the synthesis of the C13–C21 fragment of epothilones from diethyl (S)-malate
Andrei V. Bekish, Vladimir E. Isakov, Oleg G. Kulinkovich

5)

DOI:

http://dx.doi.org/10.1055/s-2004-834869

Synthesis 2005(10): 1713-1717
A Convenient Way for the Conversion of Carboxylic Esters into 2-Substituted Allyl Halides
Oleg G. Kulinkovich, Yurii Y. Kozyrkov, Andrei V. Bekish, Evgenii A. Matiushenkov, Ivan L. Lysenko


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[Chem_DM]

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