+++SD, Wiley, ACS, RCS+Chem Lett

[Anhydride]

Помогите найти статьи, пожалуйста!!!

1) Efficient solid phase synthesis of 3,5-disubstituted hydantoins
Adel Nefzi, John M. Ostresh, Marc Giulianotti and Richard A. Houghten
Tetrahedron Letters
Volume 39, Issue 45, 5 November 1998, Pages 8199-8202

Код: Выделить всё

http://dx.doi.org/10.1016/S0040-4039(98)01874-7

2) An uncatalyzed cyclo-elimination process for the release ofN3-alkylated hydantoins from solid-phase: synthesis of novel isoxazoloimidazolidinediones
Kyung-Ho Park and Mark J. Kurth
Tetrahedron Letters
Volume 40, Issue 32, 6 August 1999, Pages 5841-5844

Код: Выделить всё

http://dx.doi.org/10.1016/S0040-4039(99)01145-4

3)Solid phase hydantoin synthesis: An efficient and direct conversion of Fmoc-protected dipeptides to hydantoins
Pek Y. Chong and Peter A. Petillo
Tetrahedron Letters
Volume 40, Issue 13, 26 March 1999, Pages 2493-2496

Код: Выделить всё

http://dx.doi.org/10.1016/S0040-4039(99)00243-9

4)A modular approach to the SPOT synthesis of 1,3,5-trisubstituted hydantoins on cellulose membranes
Niklas Heine, Lothar Germeroth, Jens Schneider-Mergener and Holger Wenschuh
Tetrahedron Letters Volume 42, Issue 2, 8 January 2001, Pages 227-230

Код: Выделить всё

http://dx.doi.org/10.1016/S0040-4039(00)01960-2

5)Trapping of a phosphazide intermediate in the Staudinger reaction of tertiary phosphines with azides and its application to the synthesis of analogs of the marine alkaloid midpacamide
Pilar M. Fresneda, Marta Castañeda, Miguel A. Sanz and Pedro Molina
Tetrahedron Letters Volume 45, Issue 8, 16 February 2004, Pages 1655-1657

Код: Выделить всё

http://dx.doi.org/10.1016/j.tetlet.2003.12.117

6)Traceless synthesis of hydantoin by focused microwave irradiation
Ming-Juan Lee and Chung-Ming Sun
Tetrahedron Letters Volume 45, Issue 2, 5 January 2004, Pages 437-440

Код: Выделить всё

http://dx.doi.org/10.1016/j.tetlet.2003.10.123

7)Preparation and structure determination of two sugar amino acids via corresponding hydantoin derivatives
Miroslav Koó , Bohumil Steiner, Vratislav Langer, Dalma Gyepesová and Marián urík
Carbohydrate Research Volume 328, Issue 2, 8 September 2000, Pages 115-126

Код: Выделить всё

http://dx.doi.org/10.1016/S0008-6215(00)00099-9

Rearrangement of 2-amino-4-(trifluoromethyl)oxazoles to hydantoins
Jon P. Lawson, Karey A. VanSant
Journal of Heterocyclic Chemistry Volume 36, Issue 1, pages 283–285, January/February 1999

Код: Выделить всё

http://dx.doi.org/10.1002/jhet.5570360143

9) Synthesis of both enantiomers of 4-vinyl oxazolidin-2-one from a single precursor: D-isoascorbic acid
Giuliano Delle Monache, Domenico Misiti, Patrizia Salvatore, Giovanni Zappia
Chirality Volume 12, Issue 3, pages 143–148, 2000

Код: Выделить всё

http://dx.doi.org/10.1002/(SICI)1520-636X(2000)12:3<143::AID-CHIR7>3.0.CO;2-3

10)Preparation of (R)- and (S)-α-methyldopa from a chiral hydantoin containing the α-phenylethyl group
José Luis LeóN-Romo, Claudia I. Virues, Judit Aviña, Ignacio Regla, Eusebio Juaristi
Chirality Volume 14, Issue 2-3, pages 144–150, 2002

Код: Выделить всё

http://dx.doi.org/10.1002/chir.10043

11)A Facile Method for Preparation of Optically Active Hydantoin
Jun-ichi Yamaguchi, Masakazu Harada, Takahito Kondo, Takeshi Noda and Takayuki Suyama
Chemistry Letters Vol. 32 (2003) , No. 4 p.372

Код: Выделить всё

http://dx.doi.org/10.1246/cl.2003.372

12)Solid-Phase Synthesis of Linear Ureas Tethered to Hydantoins and Thiohydantoins
Adel Nefzi, Marcello Giulianotti, Long Truong, Somkit Rattan, John M. Ostresh, and Richard A. Houghten
J. Comb. Chem., 2002, 4 (2), pp 175–178

Код: Выделить всё

http://dx.doi.org/10.1021/cc010064l

13) Fluorous Mixture Synthesis of Fused-Tricyclic Hydantoins. Use of a Redundant Tagging Strategy on Fluorinated Substrates
Sukhdev Manku and Dennis P. Curran
J. Org. Chem., 2005, 70 (11), pp 4470–4473

Код: Выделить всё

http://dx.doi.org/10.1021/jo0502596

14)A Facile Synthesis of 1,3,5-Trisubstituted Hydantoins via Ugi Four-Component Condensation
José Miguel Ignacio, Sonia Macho, Stefano Marcaccini, Roberto Pepino, Tomás Torroba
Synlett 2005(20): 3051-3054

Код: Выделить всё

http://dx.doi.org/10.1055/s-2005-922745

15)Facile one-pot synthesis of 5-substituted hydantoins
Ross G. Murray, David M. Whitehead, Franck Le Strat and Stuart J. Conway
Org. Biomol. Chem., 2008, 6, 988 – 991

Код: Выделить всё

http://dx.doi.org/10.1039/b719675j

ОГРОМНОЕ СПАСИБО!!!!

[amik]

1-7, 12, 15

[Biginelli]

8-10, 13, 14