+++Elsevir, Wiley, ACS (total 21 art)

[Anhydride]

Помогите, пожалуйста, со статьями!
Знаю, что много

1) 2-Oxazolines (4,5-dihdro-oxazoles) by organoselenium-induced cyclisation of allylic ureas
Carmen Betancor, Elisa I. León, Thierry Prange, José A. Salazar and Ernesto Suárez
J. Chem. Soc., Chem. Commun. 1989, 8, p. 450

Код: Выделить всё

http://dx.doi.org/10.1039/C39890000450

2)Stereochemical studies-XXXIII.1 Saturated heterocycles-IX, 2: Synthesis and conformations of stereoisomeric cis- and troans-tetramethylene- and pentamethylenedihydro-1,3-oxazines
G. Bernáth, F. Fülöp, L. Gera, L. Hackler, A. Kálmán, Gy. Argay, P. Sohár
Tetrahedron Volume 35, Issue 6, 1979, Pages 799-807

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http://dx.doi.org/10.1016/0040-4020(79)80097-6

3)Stereochemical Studies. 81. Saturated Heterocycles. 69. Preparation of Methylene-bridged 3,1-Benzoxazines, 3,1-Benzoxazin-2-ones and 3,1-Benzoxazine-2-thiones
Geza Stajer, Angela E. Szabo, Ferenc Fulop, Gabor Bernath, Pal Sohar
J Het Chem 1984, Volume 21, pp. 1373-1376

Код: Выделить всё

http://dx.doi.org/10.1002/jhet.1984.5570210526

4) Configuration and NMR study of tricyclic oxazines fused to a norbornene or norbornane skeleton
P. Sohár, G. Stájer, G. Bernáth
Org Magn Reson 1983, 21(8), p 512-519

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http://dx.doi.org/10.1002/omr.1270210812

5)Stereochemische Untersuchungen, 771). - Gesättigte Heterocyclen, 641). Synthese von gesättigten Methylen-überbrückten 1,3-Benzoxazinen
Géza Stájer, Angela E. Szabó, József Szúnyog, Gábor Bernáth, Pál Sohár
Chem Ber 1984, 117(11), p 3205-3210

Код: Выделить всё

http://dx.doi.org/10.1002/cber.19841171106

6)Optisch aktives 2-Phenyl-3,4-dimethyl-morpholin
Walter G. Otto
Angew Chem 1956, 68(5), p 181-182

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http://dx.doi.org/10.1002/ange.19560680508

7) Centrally acting .alpha.1-adrenoceptor agonists based on hexahydronaphth[2,3-b]-1,4-oxazines and octahydrobenzo[g]quinolines
Joachim Nozulak, Jean M. Vigouret, Anne L. Jaton, Alfred Hofmann, Anant R. Dravid, Hans P. Weber, Hans O. Kalkman, Malcolm D. Walkinshaw
J Med Chem 1992, 35(3), pp 480–489

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http://dx.doi.org/10.1021/jm00081a008

8. Stereocontrolled synthesis of functionalized 1-azaspirans : Efficient synthesis of perhydrohistrionicotoxin
H. E. Schoemaker1 and W. N. Speckamp
Tetrahedron Volume 36, Issue 7, 1980, Pages 951-958

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http://dx.doi.org/10.1016/0040-4020(80)80047-0

9) An Efficient Synthesis of Morpholin-2-one Derivatives Using Glycolaldehyde Dimer by the Ugi Multicomponent Reaction
Young Bae Kim, Eun Hee Choi, Gyochang Keum, Soon Bang Kang, Duck Hyung Lee, Hun Young Koh, and Youseung Kim
Organic Lett 2001, 3(26), pp 4149–4152

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http://dx.doi.org/10.1021/ol016716w

10) Synthesis of Substituted-(l)-Tryptophanols from an Enantiomerically Pure Aziridine-2-methanol
Do Kyu Pyun, Cheol Hae Lee, Hyun-Joon Ha, Chan Sun Park, Jae-Won Chang, and Won Koo Lee
Organic Lett 2001, 3(26), pp 4197–4199

Код: Выделить всё

http://dx.doi.org/10.1021/ol016861+

11)Asymmetric Synthesis of (+)-Hypusine
Rajendra P. Jain, Brian K. Albrecht, Duane E. DeMong, and Robert M. Williams
Organic Lett 2001, 3(26), pp 4287–4289

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http://dx.doi.org/10.1021/ol016959o

12) Electrophilic glycinates: new and versatile templates for asymmetric amino acid synthesis
Peter J. Sinclair, Dongguan. Zhai, Joseph. Reibenspies, Robert M. Williams
JACS 1986, 108(5), pp 1103–1104

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http://dx.doi.org/10.1021/ja00265a053

13)Practical asymmetric syntheses of .alpha.-amino acids through carbon-carbon bond constructions on electrophilic glycine templates
Robert M. Williams, Peter J. Sinclair, Dongguan. Zhai, Daimo. Chen
JACS 1988, 110(5), pp 1547–1557

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http://dx.doi.org/10.1021/ja00213a031

14) Asymmetric synthesis of α-amino acids via cationic aza-cope rearrangements
Claude Agami, François Couty, Jing Lin, Axelle Mikaeloff and Michel Poursoulis
Tetrahedron Volume 49, Issue 33, 13 August 1993, Pages 7239-7250

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http://dx.doi.org/10.1016/S0040-4020(01)87201-X

15) Configurational studies on 2-[∝-(2-ethoxyphenoxy)benzyl] morpholine fce 20124
P. Melloni, A. Della Torre, E. Lazzari, G. Mazzini and M. Meroni
Tetrahedron Volume 41, Issue 7, 1985, Pages 1393-1399

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http://dx.doi.org/10.1016/S0040-4020(01)96541-X

16) Lipophilicity of Some Substituted Morpholine Derivatives Synthesized as Potential Antinociceptive Agents
Eleni Rekka, Stavros Retsas, Vassilis J. Demopoulos, Panos N. Kourounakis
Archiv der Pharmazie 1990, 323(1), p 53-56

Код: Выделить всё

http://dx.doi.org/10.1002/ardp.19903230114

17) Nitric Oxide Releasing Morpholine Derivatives as Hypolipidemic and Antioxidant Agents
Michael C. Chrysselis, Eleni A. Rekka, Ioanna C. Siskou, and Panos N. Kourounakis
J Med Chem 2002, 45(24), pp 5406–5409

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http://dx.doi.org/10.1021/jm011062i

18) Hypocholesterolemic and Hypolipidemic Activity of Some Novel Morpholine Derivatives with Antioxidant Activity
Michael C. Chrysselis, Eleni A. Rekka, and Panos N. Kourounakis
J Med Chem 2000, 43(4), pp 609–612

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http://dx.doi.org/10.1021/jm991039l

19)Efficient Synthesis of NK1 Receptor Antagonist Aprepitant Using a Crystallization-Induced Diastereoselective Transformation
Karel M. J. Brands, Joseph F. Payack, Jonathan D. Rosen, Todd D. Nelson, Alexander Candelario, Mark A. Huffman, Matthew M. Zhao, Jing Li, Bridgette Craig, Zhiguo J. Song, David M. Tschaen, Karl Hansen, Paul N. Devine, Philip J. Pye, Kai Rossen, Peter G. Dormer, Robert A. Reamer, Christopher J. Welch, David J. Mathre, Nancy N. Tsou, James M. McNamara, and Paul J. Reider
JACS 2003, 125(8), pp 2129–2135

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http://dx.doi.org/10.1021/ja027458g

20)Stereoselective Synthesis of (2R,5R)- and (2S,5R)-5-Hydroxylysine
Adrianus M. C. H. van den Nieuwendijk, Nicole M. A. J. Kriek, Johannes Brussee, Jacques H. van Boom, Arne van der Gen
Eur JOCh 2000, 22, 3683-3691

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http://dx.doi.org/10.1002/1099-0690(200011)2000:22<3683::AID-EJOC3683>3.0.CO;2-U

21)Intramolecular Chiral Relay at Stereogenic Nitrogen. Synthesis and Application of a New Chiral Auxiliary Derived from (1R,2S)-Norephedrine and Acetone
Shawn R. Hitchcock, David M. Casper, Jeremy F. Vaughn, Jennifer M. Finefield, Gregory M. Ferrence, and Joel M. Esken
JOCh 2004, 69(3), pp 714–718

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http://dx.doi.org/10.1021/jo035325n

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[SkydiVAR]

1,2,4.
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[SkydiVAR]

5-8

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А воть 3, 16, 20

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9-10-11

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12,13,17,18,19,21

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14-я и 15-я остались.

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