+++ACS, Austr J Chem, Eur ... СПАСИБО, skyforger & macro!

[Anhydride]

Пожалуйста, помогите достать статьи!!!

1. Chlorination/Cyclodehydration of Amino Alcohols with SOCl2: An Old Reaction Revisited
Feng Xu, Bryon Simmons, Robert A. Reamer, Edward Corley, Jerry Murry, and David Tschaen
J. Org. Chem., 2008, 73 (1), pp 312–315

Код: Выделить всё

http://dx.doi.org/10.1021/jo701877h

2. Cis hydroxyamination equivalent. Application to the synthesis of (-)-acosamine
Barry M. Trost, Anantha R. Sudhakar
J. Am. Chem. Soc., 1987, 109 (12), pp 3792–3794

Код: Выделить всё

http://dx.doi.org/10.1021/ja00246a054

3. Total Synthesis of (±)- and (+)-Valienamine via a Strategy Derived from New Palladium-Catalyzed Reactions
Barry M. Trost, Louis S. Chupak, and Thomas Lübbers
J. Am. Chem. Soc., 1998, 120 (8), pp 1732–1740

Код: Выделить всё

http://dx.doi.org/10.1021/ja973081g

4. Synthesis of 5-Aryloxazolidines via 1,3-Dipolar Cycloaddition Reaction of a Non-Stabilized Azomethine Ylide with Aromatic Aldehydes
John H. Ryan, Nadia Spiccia, Leon S.-M. Wong and Andrew B. Holmes
Australian Journal of Chemistry 2007, 60(12), 898–904

Код: Выделить всё

http://dx.doi.org/10.1071/CH07282

5. Synthesis of α2,2,β3-Diamino Acids by Double Stereodifferentiation Aldol Addition of Oxazolidinone Enolates to N-(tert-Butylsulfinyl) Imines (pages 3834–3844)
Andrea Guerrini, Greta Varchi, Cristian Samorì and Arturo Battaglia
European Journal of Organic Chemistry 2008, Issue 22, pages 3834–3844

Код: Выделить всё

http://dx.doi.org/10.1002/ejoc.200800356

6. New Chiral Hydroxyoxazolines Based on Ketopinic Acid and Their Use in the Asymmetric Diels-Alder Reaction
Santiago Barroso, Gonzalo Blay, Luz Cardona, José R. Pedro
Synlett 2007(17): 2659-2662

Код: Выделить всё

http://dx.doi.org/10.1055/s-2007-991052

7. Synthesis of (+)-(1R,2S,9S,9aR)-octahydro-1H-pyrrolo[1,2-a]azepine-1,2,9-triol: a potential glycosidase inhibitor
Karl B Lindsay, Stephen G Pyne
Tetrahedron Volume 60, Issue 19, 3 May 2004, Pages 4173-4176

Код: Выделить всё

http://dx.doi.org/10.1016/j.tet.2004.03.050

8. Total synthesis of the ionophore antibiotic CP-61,405 (routiennocin).
David Díez-Martin, Nikesh R. Kotecha, Steven V. Ley, Sergio Mantegani, J. Carlos Menéndez, Helen M. Organ, Andrew D. White and Bernard J. Banks
Tetrahedron Volume 48, Issue 37, 1992, Pages 7899-7938

Код: Выделить всё

http://dx.doi.org/10.1016/S0040-4020(01)80467-1

9. Synthetic study of polyoxypeptin: stereoselective synthesis of (2S,3R)-3-hydroxy-3-methylproline
Yasuo Noguchi, Hiromi Uchiro, Tatsuhiro Yamada, Susumu Kobayashi
Tetrahedron Letters Volume 42, Issue 31, 30 July 2001, Pages 5253-5256

Код: Выделить всё

http://dx.doi.org/10.1016/S0040-4039(01)00867-X

10. A novel and simple asymmetric synthesis of CMI-977 (LDP-977): a potent anti-asthmatic drug lead
Mukund K. Gurjar, A. M. S. Murugaiah, P. Radhakrishna, C. V. Ramana, Mukund S. Chorghade
Tetrahedron: Asymmetry Volume 14, Issue 10, 16 May 2003, Pages 1363-1370

Код: Выделить всё

http://dx.doi.org/10.1016/S0957-4166(03)00157-5

11. Synthesis of Schiff bases and oxazolidines from 2-amino-4-phenylthiazole
S. E. Sadigova, A. M. Magerramov and M. A. Allakhverdiev
Russian Journal of Organic Chemistry 2008, Volume 44, Number 12, 1821-1823

Код: Выделить всё

http://dx.doi.org/10.1134/S107042800812018X

ЗАРАНЕЕ ОГРОМНЕЙШЕЕ СПАСИБО!!!

[skyforger]

Высылаю первые три

[skyforger]

Пятая и шестая

[skyforger]

Седьмая, десятая, одиннадцатая
Сорри, больше нету

[macro]

4

[macro]

8

[macro]

9