+++ACS, Wiley, SD, IngConn, Thieme

[Anhydride]

Помогите, пожалуйста, очень надо

ACS
1. One-Step Synthesis of Oxazoline and Dihydrooxazine Libraries
Priyanka Chaudhry, Frank Schoenen, Benjamin Neuenswander, Gerald H. Lushington, and Jeffrey Aubé
J Comb Chem 2007, 9(3), pp 473–476

Код: Выделить всё

http://dx.doi.org/10.1021/cc060159t

2. Rhodium-Catalyzed Direct C−H Addition of 4,4-Dimethyl-2-oxazoline to Alkenes
Sean H. Wiedemann, Robert G. Bergman, and Jonathan A. Ellman
Org Lett 2004, 6(10), pp 1685–1687

Код: Выделить всё

http://dx.doi.org/10.1021/ol049417q

3. Asymmetric Conjugate Addition of Thiols to a 3-(2-Alkenoyl)-2-oxazolidinone Catalyzed by the DBFOX/Ph Aqua Complex of Nickel(II) Perchlorate
Shuji Kanemasa, Yoji Oderaotoshi, and Eiji Wada
JACS 1999, 121(37), pp 8675–8676

Код: Выделить всё

http://dx.doi.org/10.1021/ja991064g

4. 2-Amino-2-oxazolines as Subtype Selective α2 Adrenoceptor Agonists
Wai C. Wong, Wanying Sun, Weili Cui, Yuewen Chen, Carlos Forray, Pierre J.-J. Vaysse, Theresa A. Branchek, and Charles Gluchowski
J Med Chem 2000, 43(9), pp 1699–1704

Код: Выделить всё

http://dx.doi.org/10.1021/jm9905256

5. Amidines Derived from Pt(IV)-Mediated Nitrile−Amino Alcohol Coupling and Their Zn(II)-Catalyzed Conversion into Oxazolines
Anastassiya V. Makarycheva-Mikhailova, Vadim Yu. Kukushkin, Alexey A. Nazarov, Dmitrii A. Garnovskii, Armando J. L. Pombeiro, Matti Haukka, Bernhard K. Keppler, and Markus Galanski
Inorganic Chem 2003, 42(8), pp 2805–2813

Код: Выделить всё

http://dx.doi.org/10.1021/ic034070t

6. Synthetic Approach To Substituted Cyclopropanes Based on the Coupling Reaction of Lithiated Chloroalkyloxazolines with Fischer Carbene Complexes
Saverio Florio, Filippo M. Perna, Renzo Luisi, José Barluenga, Félix Rodríguez, and Francisco J. Fañanás
JOCh 2004, 69(16), pp 5480–5482

Код: Выделить всё

http://dx.doi.org/10.1021/jo049613a

7. Suzuki Cross-Coupling on Enantiomerically Pure Epoxides: Efficient Synthesis of Diverse, Modular Amino Alcohols from Single Enantiopure Precursors
Xavier Cattoën and Miquel A. Pericàs
JOCh 2007, 72(9), pp 3253–3258

Код: Выделить всё

http://dx.doi.org/10.1021/jo062612t

8. Synthesis of α- and β-Glycosyl Isothiocyanates via Oxazoline Intermediates
José L. Jiménez Blanco, Balla Sylla, Carmen Ortiz Mellet, and José M. García Fernández
JOCh 2007, 72(12), pp 4547–4550

Код: Выделить всё

http://dx.doi.org/10.1021/jo062419z

9. Chelation-Induced Axially Chiral Palladium Complex System with Tetraoxazoline Ligands for Highly Enantioselective Wacker-Type Cyclization
Yong Jian Zhang, Feijun Wang, and Wanbin Zhang
JOCh 2007, 72(24), pp 9208–9213

Код: Выделить всё

http://dx.doi.org/10.1021/jo701469y

Wiley

10. Azaenolates of 2-Chloromethyl-4-methoxymethyl-5-phenyl-2-oxazoline - A Highly Diastereo- and Enantioselective Synthesis of Oxazolinyloxiranes
Vito Capriati, Saverio Florio, Renzo Luisi
Europ JOCh 2001, 11, p 2035-2039

Код: Выделить всё

http://dx.doi.org/10.1002/1099-0690(200106)2001:11<2035::AID-EJOC2035>3.0.CO;2-R

11. Diastereoselective Synthesis of Thieno[3,2:4,5]cyclopenta[1,2-d][1,3]oxazolines - New Ligands for the Copper-Catalyzed Asymmetric Conjugate Addition of Diethylzinc to Enones
Bianca Flavia Bonini, Elena Capitò, Mauro Comes-Franchini, Alfredo Ricci, Andrea Bottoni, Fernando Bernardi, Gian Pietro Miscione, Laurent Giordano, Andrew R. Cowley
Europ JOCh 2004, 21, p 4442-4451

Код: Выделить всё

http://dx.doi.org/10.1002/ejoc.200400351

12. Effects of Extended Aryl-Substituted Bisoxazoline Ligands in Asymmetric Synthesis - Efficient Synthesis and Application of 4,4-Bis(1-Naphthyl)-, 4,4-Bis(2-Naphthyl)- and 4,4-Bis(9-Anthryl)-2,2-isopropylidenebis(1,3-oxazolines)
Hester L. van Lingen, Floris L. van Delft, Roy P. M. Storcken, Koen F. W. Hekking, Anouk Klaassen, Jan J. M. Smits, Patrycja Ruskowska, Jadwiga Frelek, Floris P. J. T. Rutjes
Europ JOCh 2005, 23, p 4975-4987

Код: Выделить всё

http://dx.doi.org/10.1002/ejoc.200500566

13. Sulfonamide Ligands Attained Through Opening of Saccharin Derivatives
Richard I. Robinson, Ross Fryatt, Claire Wilson, Simon Woodward
Europ JOCh 2006, 19, p 4483-4489

Код: Выделить всё

http://dx.doi.org/10.1002/ejoc.200600508

SD

14. The application of the intermediate 2-methyl-glyco-[2,1-d]-2-oxazolines for glycoside synthesis
Sergey S. Pertel, Vasily Ya. Chirva, Andrey L. Kadun and Elena S. Kakayan
Carbohydrate Research Volume 329, Issue 4, 1 December 2000, Pages 895-899

Код: Выделить всё

http://dx.doi.org/10.1016/S0008-6215(00)00237-8

15. Cyclopentathiophene-alkyloxazolines: new nitrogen–sulfur hybrid ligands and their use in asymmetric palladium-catalyzed allylic alkylation
Bianca-Flavia Boninia, Laurent Giordanob, Mariafrancesca Fochia, Mauro Comes-Franchinia, Luca Bernardia, Elena Capitòa and Alfredo Ricci
Tetrahedron: Asymmetry Volume 15, Issue 6, 22 March 2004, Pages 1043-1051

Код: Выделить всё

http://dx.doi.org/10.1016/j.tetasy.2004.01.036

Ingenta Connect

16. Thermal cyclisation of β-hydroxyamides to oxazolines
Authors: Somanathan, Ratnasamy; Aguilar, Hugo R.; Rivero, Ignacio A.; Aguirre, G.; Hellberg, Lars H.; Yu, Zheng; Thomas, Jacquelyn A.
Journal of Chemical Research, Volume 2001, Number 3, March 2001, pp. 92-92(1)

Код: Выделить всё

http://dx.doi.org/10.3184/030823401103169225

Georg Thieme Verlag

17. Enantioselective Diels-Alder Reactions: Effect of the Achiral Template on Reactivity and Selectivity
Mukund P. Sibi, Jianxie Chen, Levi Stanley
Synlett 2007, 2, 298-302

Код: Выделить всё

http://dx.doi.org/10.1055/s-2007-968014

18. A Novel and Chemoselective Synthesis of 2-Aryloxazolines and Bis-oxazolines Catalyzed by Bi(III) Salts
Iraj Mohammadpoor-Baltork, Ahmad Reza Khosropour, Seyedeh Fatemeh Hojati
Synlett 2005, 18, 2747-2750

Код: Выделить всё

http://dx.doi.org/10.1055/s-2005-918951

19. Silver-Catalyzed Preparation of Oxazolines from N-Propargylamides
Michael Harmata, Chaofeng Huang
Synlett 2008, 9, 1399-1401

Код: Выделить всё

http://dx.doi.org/10.1055/s-2008-1078405

ОГРОМНЕЙШЕЕ СПАСИБО ЗАРАНЕЕ!!!

[nikolay_ap]

1 - 4

[nikolay_ap]

5 - 7

[nikolay_ap]

8 - 10

[nikolay_ap]

11 - 13

[Viksya]

15

[nikolay_ap]

14

[nikolay_ap]

18

[nikolay_ap]

В 17 работе проверьте DOI... "Error - DOI Naming Authority [110.1055] Not Found"

[Anhydride]

В 17-м все исправил. Единичка лишняя затисалась...

[nikolay_ap]

17

[Anhydride]

Осталось всего 2 шт...16 и19!
Спасибо за помощь, nikolay_ap и Viksya!!!

[mlkost]

+19

[Abwer]

16