+++ 10 Tetrahedrol Letters + 3 Tetrahedron

[OrganicChemist]

Уважаемые коллеги, помогите пожалуйста скачать:

1. Formal total synthesis of borrelidin: synthesis of C1–C11 fragment via desymmetrization strategy
J.S. Yadav, Padmavani Bezawadaa and Venugopal Chenna

Tetrahedron Letters
Volume 50, Issue 27, 8 July 2009, Pages 3772-3775

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http://dx.doi.org/10.1016/j.tetlet.2009.03.196  

2. Tulearins A, B, and C; structures and absolute configurations
Ashgan Bishara, Amira Rudi, Israel Goldberg, Maurice Aknin and Yoel Kashman

Tetrahedron Letters
Volume 50, Issue 27, 8 July 2009, Pages 3820-3822

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http://dx.doi.org/10.1016/j.tetlet.2009.04.028  

3. Stereoselective synthesis of tubuvaline methyl ester and tubuphenylalanine, components of tubulysins, tubulin polymerization inhibitors
Taku Shibue, Toshihiro Hirai, Iwao Okamoto, Nobuyoshi Morita, Hyuma Masu, Isao Azumaya and Osamu Tamura

Tetrahedron Letters
Volume 50, Issue 27, 8 July 2009, Pages 3845-3848

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http://dx.doi.org/10.1016/j.tetlet.2009.04.046  

4. Highly stereoselective synthesis of vicinal diols by stannous chloride-mediated addition of hydroxyallylic stannanes to aldehydes
Makoto Yasuda, Tatsuya Azuma, Kensuke Tsuruwa, Srinivasarao Arulananda Babu and Akio Baba

Tetrahedron Letters
Volume 50, Issue 26, 1 July 2009, Pages 3209-3212

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http://dx.doi.org/10.1016/j.tetlet.2009.01.137    

5. Synthesis of all the four stereoisomers of (1′S)-1-ethyl-2-methylpropyl 3,13-dimethylpentadecanoate, the major component of the sex pheromone of Paulownia bagworm, Clania variegata
Kenji Mori and Takuya Tashiro

Tetrahedron Letters
Volume 50, Issue 26, 1 July 2009, Pages 3266-3269

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http://dx.doi.org/10.1016/j.tetlet.2009.02.046    

6. Stereoflexible total synthesis of (−)-epiquinamide
S. Chandrasekhar, Bibhuti Bhusan Paridaa and Ch. Rambabu

Tetrahedron Letters
Volume 50, Issue 26, 1 July 2009, Pages 3294-3295

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http://dx.doi.org/10.1016/j.tetlet.2009.02.051     

7. Ti(III)-mediated radical cyclization of β-aminoacrylate containing epoxy alcohol moieties: synthesis of highly substituted azacycles
Tushar Kanti Chakrabortya, Rajarshi Samanta, Saumya Roy and Balasubramanian Sridha

Tetrahedron Letters
Volume 50, Issue 26, 1 July 2009, Pages 3306-3310

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http://dx.doi.org/10.1016/j.tetlet.2009.02.063      

8. Synthetic studies on amphidinolides C and F: synthesis of the C18–C29 segment of amphidinolide
Alan Armstrong and Constantina Pyrkotis

Tetrahedron Letters
Volume 50, Issue 26, 1 July 2009, Pages 3325-3328

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http://dx.doi.org/10.1016/j.tetlet.2009.02.093        

9. Pentadienyl sulfoxide in triene synthesis. Efficient assembly of the Northern fragment of polycavernoside A
Pierre Jourdain, Freddi Philippart, Raphaël Dumeunierb and Istvan E. Markó

Tetrahedron Letters
Volume 50, Issue 26, 1 July 2009, Pages 3366-3370

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http://dx.doi.org/10.1016/j.tetlet.2009.02.118      

10. Total synthesis and determination of the absolute stereochemistry of the squalene synthase inhibitors CJ-13,981 and CJ-13,982
Frederick Calo, Alexander Bondke, Jeffery Richardsonb, Andrew J.P. White and Anthony G.M. Barret

Tetrahedron Letters
Volume 50, Issue 26, 1 July 2009, Pages 3388-3390

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http://dx.doi.org/10.1016/j.tetlet.2009.02.121     

11. Hemisynthesis and absolute configuration of novel 6-pentyl-2H-pyran-2-one derivatives from Trichoderma spp.
Mourad Daoubi, Cristina Pinedo-Rivilla, M. Belén Rubio, Rosa Hermosa, Enrique Monte, Josefina Aleu and Isidro G. Collado

Tetrahedron
Volume 65, Issue 25, 20 June 2009, Pages 4834-4840

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http://dx.doi.org/10.1016/j.tet.2009.04.051       

12. The synthesis of novel hexa-13C-labelled glucosinolates from [13C6]-d-glucose
Qingzhi Zhang, Tomas Lebl, Agnieszka Kulczynska and Nigel P. Botting

Tetrahedron
Volume 65, Issue 25, 20 June 2009, Pages 4871-4876

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http://dx.doi.org/10.1016/j.tet.2009.04.043     

13. Synthetic evaluation of an enantiopure tetrahydropyridine N-oxide. Synthesis of (+)-febrifugine
Amir Ashoorzadeh, Glenn Archibald and Vittorio Caprio

Tetrahedron
Volume 65, Issue 24, 13 June 2009, Pages 4671-4680

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http://dx.doi.org/10.1016/j.tet.2009.04.044        

Спасибо всем !!!

[Myrsten]

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[OrganicChemist]

Спасибо, Myrsten, за оперативность.