+++JHetChem, Chem Comm, Chem Ber, AccChemRes

[Anhydride]

Помогите, пожалуйста, со статейками!!!
Знаю, что много, но мож к-нибудь совмесными усилиями и соберется....

1. New Oxazinone and Pyrazinone Derivatives as Chiral Reagents for the Asymmetric Synthesis of a-Amino Acids
Tomas Abellan, Rafael Chinchilla, Nuria Galindo, Carmen Najera, Jose M. Sansano
J Het Chem 2000, Volume 37, pp. 467-479

Код: Выделить всё

https://www.jhetchem.com/cd2html.php?file=20000467

2. Chiral Oxazolines - Their Legacy as Key Players in the Renaissance of Asymmetric Synthesis
A.I. Meyers
J Het Chem 1998, Volume 35, Abstracts, pp. 991-1002

Код: Выделить всё

https://www.jhetchem.com/cd2html.php?file=19980991

3. Palladium-catalysed cross double carbonylation of amines and alcohols: synthesis of oxamates
Shun-Ichi Murahashi, Yo Mitsue and Kazuo Ike
J. Chem. Soc., Chem. Commun., 1987, 2, p.125

Код: Выделить всё

http://dx.doi.org/10.1039/C39870000125

4. Aminoalkohole, XXIV. Notiz über 4-Methyl- und 4-Cyclohexyl-morpholin-dion-(2.3)
Günther Drefahl, Manfred Hartmann, Axel Skurk
Chem Ber 1966, 99(8), p 2716-2717

Код: Выделить всё

http://dx.doi.org/10.1002/cber.19660990847

5. Enantioselective Free Radical Reactions
Mukund P. Sibi and Ned A. Porter
Acc. Chem. Res. 1999, 32 (2), pp 163–171

Код: Выделить всё

http://dx.doi.org/10.1021/ar9600547

6. Chiral Bis(oxazoline) Copper(II) Complexes: Versatile Catalysts for Enantioselective Cycloaddition, Aldol, Michael, and Carbonyl Ene Reactions
Jeffrey S. Johnson and David A. Evans
Acc. Chem. Res. 2000, 33 (6), pp 325–335

Код: Выделить всё

http://dx.doi.org/10.1021/ar960062n

7. Asymmetric carbon-carbon bond formation from chiral oxazolines
Albert I. Meyers
Acc. Chem. Res. 1978, 11 (10), pp 375–381

Код: Выделить всё

http://dx.doi.org/10.1021/ar50130a002

8. The Chemistry of Dimethyl Carbonate
Pietro Tundo and Maurizio Selva
Acc. Chem. Res. 2002, 35 (9), pp 706–716

Код: Выделить всё

http://dx.doi.org/10.1021/ar010076f

9. The Use of a Mannitol-Derived Fused Oxacycle as a Combinatorial Scaffold
Mattie S. M. Timmer, Martijn Verdoes, Leo A. J. M. Sliedregt, Gijsbert A. van der Marel, Jacques H. van Boom, and Herman S. Overkleeft
JOCh 2003, 68(24), pp 9406–9411

Код: Выделить всё

http://dx.doi.org/10.1021/jo0349429

10. Recent Developments in the Ring-Chain Tautomerism of 1,3-Heterocycles
László Lázár, Ferenc Fülöp
Europ JOCh 2003, 16, p 3025-3042

Код: Выделить всё

http://dx.doi.org/10.1002/ejoc.200300142

11. The Use of N-Boc-1,3-Oxazolidines as Chiral Auxiliaries in Asymmetric Synthesis
Claude Agami, François Couty
Europ JOCh 2004, 4, p 677-685

Код: Выделить всё

http://dx.doi.org/10.1002/ejoc.200300452

12. Synthesis and Structural Analysis of Cyclic Oligomers Consisting of Furanoid and Pyranoid -Sugar Amino Acids
Renate M. van Well, Luciana Marinelli, Kees Erkelens, Gijsbert A. van der Marel, Antonio Lavecchia, Herman S. Overkleeft, Jacques H. van Boom, Horst Kessler, Mark Overhand
Europ JOCh 2003, 12, p 2303-2313

Код: Выделить всё

http://dx.doi.org/10.1002/ejoc.200300031

13. Original Synthesis of Linear, Branched and Cyclic Oligoglycerol Standards Stephanie Cassel, Catherine Debaig, Thierry Benvegnu, Patrick Chaimbault, Michel Lafosse, Daniel Plusquellec, Patrick Rollin
Europ JOCh 2001, 5, p 875-896

Код: Выделить всё

http://dx.doi.org/10.1002/1099-0690(200103)2001:5<875::AID-EJOC875>3.0.CO;2-R

14. Regioselective and Stereospecific Synthesis of Enantiopure 1,3-Oxazolidin-2-ones by Intramolecular Ring Opening of 2-(Boc-aminomethyl)aziridines. Preparation of the Antibiotic Linezolid
Roberto Moran-Ramallal, Ramon Liz and Vicente Gotor
Org Lett 2008, 10(10), pp 1935–1938

Код: Выделить всё

http://dx.doi.org/10.1021/ol800443p

15. Enantiopure 1,5-Diols from Dynamic Kinetic Asymmetric Transformation. Useful Synthetic Intermediates for the Preparation of Chiral Heterocycles
Karin Leijondahl, Linnea Boren, Roland Braun and Jan-E. Backvall
Org Lett 2008, 10(10), pp 2027–2030

Код: Выделить всё

http://dx.doi.org/10.1021/ol800468h

16. Facile Route to 3,5-Disubstituted Morpholines: Enantioselective Synthesis of O-Protected trans-3,5-Bis(hydroxymethyl)morpholines
Rajesh Dave and N. André Sasaki
Org Lett 2004, 6(1), pp 15–18

Код: Выделить всё

http://dx.doi.org/10.1021/ol035998s

17. Bromoethylsulfonium SaltA More Effective Annulation Agent for the Synthesis of 6- and 7-Membered 1,4-Heterocyclic Compounds
Muhammad Yar, Eoghan M. McGarrigle and Varinder K. Aggarwal
Org Lett 2009, 11(2), pp 257–260

Код: Выделить всё

http://dx.doi.org/10.1021/ol8023727

18. Asymmetric Synthesis of (+)-(S,S)-Reboxetine via a New (S)-2-(Hydroxymethyl)morpholine Preparation
Eric Brenner, Ronald M. Baldwin, and Gilles Tamagnan
Org Lett 2005, 7(5), pp 937–939

Код: Выделить всё

http://dx.doi.org/10.1021/ol050059g

19. Umpolung of Chiral 2-Ethynylaziridines: Indium(I)-Mediated Stereoselective Synthesis of Nonracemic 1,3-Amino Alcohols Bearing Three Chiral Centers, Catalyzed by Palladium(0)
Hiroaki Ohno, Hisao Hamaguchi, and Tetsuaki Tanaka
Org Lett 2000, 2(14), pp 2161–2163

Код: Выделить всё

http://dx.doi.org/10.1021/ol006089v

20. Chemical structure-fungicidal activity relationships in substituted morpholines Ernst-Heinrich Pommer
Pesticide Sci 1984, 15(3), p 285-295

Код: Выделить всё

http://dx.doi.org/10.1002/ps.2780150311

21. Stereocontrolled Asymmetric Synthesis of α-Hydroxy-β-amino Acids. A Stereodivergent Approach
Yutaka Aoyagi, Rajendra P. Jain, and Robert M. Williams
JACS 2001, 123(15), pp 3472–3477

Код: Выделить всё

http://dx.doi.org/10.1021/ja0042332

22. Halonium-initiated cyclizations of allylic urethanes: stereo- and regioselectivity in functionalizing the olefinic bond
Kathlyn A. Parker, Robert O'Fee
JACS 1983, 105(3), pp 654–655

Код: Выделить всё

http://dx.doi.org/10.1021/ja00341a073

23. Perspectives on 1,4-Benzodioxins, 1,4-Benzoxazines and their 2,3-Dihydro Derivatives
Basudeb Achari, Sukhendu B. Mandal, Pradeep K. Dutta, Chinmay Chowdhury
Synlett 2004, 14, 2449-2467

Код: Выделить всё

http://dx.doi.org/10.1055/s-2004-834816

24. A Straightforward Synthesis of Enantiopure 2,6-Disubstituted Morpholines by a Regioselective O-Protection/Activation Protocol
Michele Penso, Vittoria Lupi, Domenico Albanese, Francesca Foschi, Dario Landini, Aaron Tagliabue
Synlett 2008, 16, 2451-2454

Код: Выделить всё

http://dx.doi.org/10.1055/s-2008-1078054

25. Insertion of the methylene-oxy surrogate of the amide bond into Boc-Val-Leu-OH: X-ray crystal structure, solution conformation and molecular modelling study
Gérald Villeneuve, John DiMaio, Marc Drouin and André G. Michel,
J. Chem. Soc., Perkin Trans. 2, 1994, 7, p.1631

Код: Выделить всё

http://dx.doi.org/10.1039/P29940001631

ОГРОМНОЕ ВСЕМ СПАСИБО ЗАРАНЕЕ!!!

[Viksya]

Фигассе
Ну воть 4

[Viksya]

А воть 10, 11, 12, 13

[Viksya]

А воть 20

[Viksya]

А слабо было 1 и 2 ссылку с Вилея дать, а???
Воть 1,2

[macro]

24

[macro]

23

[macro]

22

[macro]

21

[macro]

19

[macro]

17

[macro]

18

[macro]

14, 15

[macro]

5-8

[mlkost]

+9 и 16
И, если не ошибся, остались 3 и 25

[Himera]

3, 25