+++ 19 из Tetrahedron: Asymmetry (SD) CПАСИБО !

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1. A simple entry into 1,3-diols from (R)-2,3-cyclohexylideneglyceraldehyde: synthesis of (−)-galantinic acid
Bhaskar Dhotarea and Angshuman Chattopadhyay

Tetrahedron: Asymmetry
Volume 20, Issue 17, 8 September 2009, Pages 2007-2013

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 http://dx.doi.org/10.1016/j.tetasy.2009.07.030         

2. Metal-dependent modulation of diastereoselectivity in the Barbier-type crotylation of (R)-cyclohexylideneglyceraldehyde
Dibakar Goswami, Angshuman Chattopadhyay and Subrata Chattopadhyay

Tetrahedron: Asymmetry
Volume 20, Issue 17, 8 September 2009, Pages 1957-1961

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 http://dx.doi.org/10.1016/j.tetasy.2009.08.013           

3. Synthesis of C18–C28 ketone fragment of micromonospolide B possessing 1,3-diene and 1,3-anti-diol functionalities
Liang Suna, Jinlong Wua and Wei-Min Dai

Tetrahedron: Asymmetry
Volume 20, Issue 16, 26 August 2009, Pages 1864-1870

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 http://dx.doi.org/10.1016/j.tetasy.2009.07.042             

4. Stereoselective total synthesis of simplactone A
Ahmed Kamal, Papagari Venkat Reddy, Singaraboina Prabhakar and Paidakula Suresh

Tetrahedron: Asymmetry
Volume 20, Issue 15, 12 August 2009, Pages 1798-1801

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 http://dx.doi.org/10.1016/j.tetasy.2009.07.008               

5. Asymmetric synthesis of a sex pheromone (3S,5R,6S)-3,5-dimethyl-6-isopropyl-3,4,5,6-tetrahydropyran-2-one
Peddikotla Prabhakar, Singanaboina Rajaram and Yenamandra Venkateswarlu

Tetrahedron: Asymmetry
Volume 20, Issue 15, 12 August 2009, Pages 1806-1808

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 http://dx.doi.org/10.1016/j.tetasy.2009.07.019                 

6. Application of a modified Mosher’s method for the determination of enantiomeric ratio and absolute configuration at C-3 of chiral 1,3-dihydroxy ketones
James L. Galman and Helen C. Hailes

Tetrahedron: Asymmetry
Volume 20, Issue 15, 12 August 2009, Pages 1828-1831

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 http://dx.doi.org/10.1016/j.tetasy.2009.07.023                   

7. Pyroglutamic acid: a unique chiral synthon
Sharad Kumar Panday, Jagdish Prasad and Dinesh Kumar Dikshit

Tetrahedron: Asymmetry
Volume 20, Issue 14, 29 July 2009, Pages 1581-1632

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 http://dx.doi.org/10.1016/j.tetasy.2009.06.011                     

8. Stereoselective total synthesis of polyketide lactone, (3R,4S,5S,9S)-3,5,9-trihydroxy-4-methylundecanoic acid δ-lactone
Gowravaram Sabitha, Peddabuddi Gopal and Jhillu S. Yadav

Tetrahedron: Asymmetry
Volume 20, Issue 13, 16 July 2009, Pages 1493-1499

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 http://dx.doi.org/10.1016/j.tetasy.2009.06.008                 

9. Novel fungi-catalyzed reduction of α-alkyl-β-keto esters
Silvana P. Ravía, Ignacio Carrera, Gustavo A. Seoane, Silvana Vero and Daniela Gamenara

Tetrahedron: Asymmetry
Volume 20, Issue 12, 2 July 2009, Pages 1393-1397

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 http://dx.doi.org/10.1016/j.tetasy.2009.05.031                    

10. A new synthesis of the phytotoxic 10-membered lactone herbarumin I
J. Jon Paul Selvam, K. Rajesh, V. Suresh, D. Chanti Babu and Y. Venkateswarlu

Tetrahedron: Asymmetry
Volume 20, Issue 10, 5 June 2009, Pages 1115-1119

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 http://dx.doi.org/10.1016/j.tetasy.2009.03.034                      

11. A chemoenzymatic asymmetric synthesis of methyl (6S,13R)-6,13-dihydroxytetradeca-(2E,4E,8E)-trienoate, a component of Mycosphaerella rubella
Anubha Sharma, Sunita Gamre and Subrata Chattopadhyay

Tetrahedron: Asymmetry
Volume 20, Issue 10, 5 June 2009, Pages 1164-1167

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 http://dx.doi.org/10.1016/j.tetasy.2009.04.004                        

12. On the microbial reduction of ethyl α-methylacetoacetate
Aline de Souza Ramos, Joyce Benzaquem Ribeiro

Tetrahedron: Asymmetry
Volume 20, Issue 5, 25 March 2009, Pages 559-561

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 http://dx.doi.org/10.1016/j.tetasy.2009.03.011                      

13. Catalytic enantioselective synthesis of axially chiral allenes
Masamichi Ogasawara

Tetrahedron: Asymmetry
Volume 20, Issue 3, 26 February 2009, Pages 259-271

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 http://dx.doi.org/10.1016/j.tetasy.2008.11.039                       

14. Synthesis and spectroscopic correlation of the diastereoisomers of 2,3-dihydroxy-2,6,8-trimethyldeca-(4Z,6E)-dienoic acid: implications for the structures of papuamides A–D and mirabamides A–D
Gurusankar Ramamoorthy, Cristina M. Acevedo, Edgardo Alvira and Mark A. Lipton

Tetrahedron: Asymmetry
Volume 19, Issue 22, 17 November 2008, Pages 2546-2554

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 http://dx.doi.org/10.1016/j.tetasy.2008.09.031                      

15. Stereoselective synthesis of (3R,4S)-3-amino-4-methyl pyrrolidine
G. Jayachitra, Ravi Kumar Anchoori and B. Venkateswara Rao

Tetrahedron: Asymmetry
Volume 19, Issue 20, 20 October 2008, Pages 2402-2405

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 http://dx.doi.org/10.1016/j.tetasy.2008.10.005                     

16. Concise asymmetric syntheses of the (+)-2-C-methyltetritol isomers
Anubha Sharma, Priyadip Das and Subrata Chattopadhyay

Tetrahedron: Asymmetry
Volume 19, Issue 18, 22 September 2008, Pages 2167-2170

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 http://dx.doi.org/10.1016/j.tetasy.2008.09.002                      

17. Stereoselective synthesis of a C1–C6 fragment of pinnatoxin A via a 1,4-addition/alkylation sequence
Seiichi Nakamura, Fumiaki Kikuchi and Shunichi Hashimoto

Tetrahedron: Asymmetry
Volume 19, Issue 9, 16 May 2008, Pages 1059-1067

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 http://dx.doi.org/10.1016/j.tetasy.2008.04.013                      

18. Synthesis of the (5S,9R)-isomer of 5,9-dimethylpentadecane, the major component of the female sex pheromone of the coffee leaf miner moth, Leucoptera coffeellastar
Kenji Mori

Tetrahedron: Asymmetry
Volume 19, Issue 7, 17 April 2008, Pages 857-861

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 http://dx.doi.org/10.1016/j.tetasy.2008.03.016                        

19. Total synthesis of (−)-lentiginosine
S. Chandrasekhar, B.V.D. Vijaykumar and T.V. Pratap

Tetrahedron: Asymmetry
Volume 19, Issue 6, 3 April 2008, Pages 746-750

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 http://dx.doi.org/10.1016/j.tetasy.2008.02.017                      

Заранее с пасибо всем большое !!!

[LEDI]

1, 2

[LEDI]

Следующие 4

[OrganicChemist]

Спасибо.

[LEDI]

8-12

[OrganicChemist]

9 и 12 не зачитались, перезалейте, 7-й нету !!!

[LEDI]

13-19..

[OrganicChemist]

19 не зачиталась тоже.

[LEDI]

Повтор

[LEDI]

И ещё повтор

[OrganicChemist]

Только 7 нету и все !!!.

[LEDI]

9, 12, 19 перезалиты

[OrganicChemist]

Только 7 нету и все !!!.

[LEDI]

7 скоро будет, объемчик велик

[LEDI]

7 долгожданная

[OrganicChemist]

Спасибо большое, милая и прекрасная LEDI