+++ChemLett, JACS, ChemComm, OL, Perkin, TL, SComm, AccChRes

[Anhydride]

Здравствуйте!
Помогите, пожалуйста, со статьями

1. Enantiospecific Construction of Quaternary Carbon Center via Intramolecular 1,3-Dipolar Cycloaddition. A New Route to Natural (−)-Mesembrine from (S)-O-Benzylglycidol
Seiichi Takano, Kiyohiro Samizu and Kunio Ogasawara
Chemistry Letters Volume 19 Number 7 Year 1990 Page 1239-1242

Код: Выделить всё

http://dx.doi.org/10.1246/cl.1990.1239

2. Inversion of Stereochemistry in the Co2(CO)8-Catalyzed Carbonylation of Aziridines to β-Lactams. The First Synthesis of Highly Strained trans-Bicyclic β-Lactams
Marcelo E. Piotti and Howard Alper
J. Am. Chem. Soc., 1996, 118 (1), pp 111–116

Код: Выделить всё

http://dx.doi.org/10.1021/ja9531586

3. Bromine-Catalyzed Aziridination of Olefins. A Rare Example of Atom-Transfer Redox Catalysis by a Main Group Element
Jae Uk Jeong, Beata Tao, Ingo Sagasser, Hans Henniges, and K. Barry Sharpless
J. Am. Chem. Soc., 1998, 120 (27), pp 6844–6845

Код: Выделить всё

http://dx.doi.org/10.1021/ja981419g

4. A concise enantioselective route to (–)-kainic acid from (S)-2-(benzyloxymethyl)oxirane
Seiichi Takano, Yoshiharu Iwabuchi and Kunio Ogasawara
J. Chem. Soc., Chem. Commun., 1988, 1204-1206

Код: Выделить всё

http://dx.doi.org/10.1039/C39880001204

5. Copper-Catalyzed Alkene Aziridination with N-Tosyloxycarbamates
Hélène Lebel, Sylvain Lectard, and Michaël Parmentier
Org. Lett., 2007, 9 (23), pp 4797–4800

Код: Выделить всё

http://dx.doi.org/10.1021/ol702152e

6. Convenient Synthesis of trans-β-Amino Carboxylic Esters with an Azetidine Skeleton via Rearrangement of β,γ-Aziridino α-amino Esters
Loránd Kiss, Sven Mangelinckx, Ferenc Fülöp, and Norbert De Kimpe
Org. Lett., 2007, 9 (21), pp 4399–4402

Код: Выделить всё

http://dx.doi.org/10.1021/ol7020466

7. Cyclization of Lithiated Pyridine and Quinoline Carboxamides: Synthesis of Partially Saturated Pyrrolopyridines and Spirocyclic β-Lactams
Jonathan Clayden, Stuart D. Hamilton, and Rukhsana T. Mohammed
Org. Lett., 2005, 7 (17), pp 3673–3676

Код: Выделить всё

http://dx.doi.org/10.1021/ol051214u

8. Control of Enantioselectivity in the Photochemical Conversion of α-Oxoamides into β-Lactam Derivatives
Arunkumar Natarajan, Keyan Wang, V. Ramamurthy, John R. Scheffer, and Brian Patrick
Org. Lett., 2002, 4 (9), pp 1443–1446

Код: Выделить всё

http://dx.doi.org/10.1021/ol025700i

9. Transition Metal Mediated Carbonylative Ring Expansion of Heterocyclic Compounds
Kanjai Khumtaveeporn, Howard Alper
Acc. Chem. Res., 1995, 28 (10), pp 414–422

Код: Выделить всё

http://dx.doi.org/10.1021/ar00058a003

10. A new synthetic strategy for the penems. Total synthesis of (5R,6S,8R)-6-(.alpha.-hydroxyethyl)-2-(hydroxymethyl)penem-3-carboxylic acid
Stephen Hanessian, Angelo Bedeschi, Carlo Battistini, Nicola Mongelli
J. Am. Chem. Soc., 1985, 107 (5), pp 1438–1439

Код: Выделить всё

http://dx.doi.org/10.1021/ja00291a069

11. cis-Selective aziridination of cis- or trans-α,β-unsaturated amides using diaziridine
Kiyoto Hori, Hiroyasu Sugihar, Yoshio N. Ito, Tsutomu Katsuki
Tetrahedron Letters Volume 40, Issue 28, 9 July 1999, Pages 5207-5210

Код: Выделить всё

http://dx.doi.org/10.1016/S0040-4039(99)00939-9

12. Microwave-Assisted Regioselective Synthesis of trans-1-Arenesulfonyl-2-ethoxycarbonyl-3-phenylazetidines
Sarika Malik; Upender K. Nadir; Pramod S. Pandey
Synthetic Communications, Volume 40, Issue 11 January 2010 , pages 1631 – 1638

Код: Выделить всё

http://dx.doi.org/10.1080/00397910903136100

13. Reaction of N-arylsulfonylaziridines with dimethylsulfoniumethoxycarbonyl methylide: regio- and stereo-selective synthesis of 1-arylsulfonyl-2-ethoxycarbonyl azetidines
Upender K. Nadir and Anjali Arora
J. Chem. Soc., Perkin Trans. 1, 1995, #20, 2605-2610

Код: Выделить всё

http://dx.doi.org/10.1039/P19950002605

14. Penaresidin A and B, two novel azetidine alkaloids with potent actomyosin ATPase-activating activity from the Okinawan marine sponge Penares sp.
Jun'ichi Kobayashi, Jie-Fei Cheng, Masami Ishibashi, Markus R. Wälchli, Shosuke Yamamura and Yasushi Ohizumi
J. Chem. Soc., Perkin Trans. 1, 1991, #5, 1135-1138

Код: Выделить всё

http://dx.doi.org/10.1039/P19910001135

Большое спасибо заранее!!!

[iskariot]

2-10

[iskariot]

12-14

[Anhydride]

СПАСИБО, iskariot!!!

[Arkadii_Tarasevych]

1, 11