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1. Microwave-assisted regioselective ring opening of non-activated aziridines by lithium aluminium hydride
Sonja Stankovi?, Matthias D'hooghe and Norbert De Kimpe
Org. Biomol. Chem., 2010, 8(19), 4266-4273

DOI:

http://dx.doi.org/10.1039/C004960C

2. Chiral phosphine oxides in present-day organocatalysis
Maurizio Benaglia and Sergio Rossi
Org. Biomol. Chem., 2010, 8(17), 3824-3830

DOI:

http://dx.doi.org/10.1039/C004681G

3. Recent advances in transition metal-catalyzed N-atom transfer reactions of azides
Tom G. Driver
Org. Biomol. Chem., 2010, 8(17), 3831-3846

DOI:

http://dx.doi.org/10.1039/C005219C

4. Flexible and enantioselective access to jaspine B and biologically active chain-modified analogues thereof
Yahya Salma, St?phanie Ballereau, Carine Maaliki, Sonia Ladeira, Nathalie Andrieu-Abadie and Yves G?nisson
Org. Biomol. Chem., 2010, 8(14), 3227-3243

DOI:

http://dx.doi.org/10.1039/C004218H

5. Chemistry of the cortistatins–a novel class of anti-angiogenic agents
David Yu-Kai Chen and Chih-Chung Tseng
Org. Biomol. Chem., 2010, 8(13), 2900-2911

DOI:

http://dx.doi.org/10.1039/C003935G

6. Structure and reactivity of bicyclic methylene aziridines prepared by intramolecular aziridination of allenes
Jeremy Robertson, George C. Feast, Louise V. White, Victoria A. Steadman (n?e Doughty) and Timothy D. W. Claridge
Org. Biomol. Chem., 2010, 8(13), 3060-3063

DOI:

http://dx.doi.org/10.1039/C003693E

7. Synthesis of oxazolidinones initiated by regio- and diastereo-controlled crotylation of ?-dicarbonyl compounds
Ikuya Shibata, Ryota Kojima, Shinji Tsunoi, Takashi Nozaki, Tomonari Watanabe, Atsushi Ninomiya, Makoto Yasuda and Akio Baba
Org. Biomol. Chem., 2010, 8(9), 2009-2011

DOI:

http://dx.doi.org/10.1039/C000197J

8. Chemoenzymatic synthesis of chiral 2,2?-bipyridine ligands and their N-oxide derivatives: applications in the asymmetric aminolysis of epoxides and symmetric allylation of aldehydes
D. R. Boyd, N. D. Sharma, L. Sbircea, D. Murphy, J. F. Malone, S. L. James, C. C. R. Allen and J. T. G. Hamilton
Org. Biomol. Chem., 2010, 8(5), 1081-1090

DOI:

http://dx.doi.org/10.1039/B919894F

9. Stereoselective synthesis of trans- and cis-2-aryl-3-(hydroxymethyl)aziridines through transformation of 4-aryl-3-chloro-?-lactams and study of their ring opening
Matthias D'hooghe, Karen Mollet, Stijn Dekeukeleire and Norbert De Kimpe
Org. Biomol. Chem., 2010, 8(3), 607-615

DOI:

http://dx.doi.org/10.1039/B919864D

10. An efficient copper-catalyzed synthesis of hexahydro-1H-phenothiazines
D. J. C. Prasad and Govindasamy Sekar
Org. Biomol. Chem., 2009, 7(24), 5091-5097

DOI:

http://dx.doi.org/10.1039/B916664E

11. Towards a chemo-enzymatic method for the asymmetric synthesis of ?-amino tertiary alcohols
Andrea March-Cortijos and Timothy J. Snape
Org. Biomol. Chem., 2009, 7(24), 5163-5165

DOI:

http://dx.doi.org/10.1039/B916013B

12. Rediscovering copper-based catalysts for intramolecular carbon–hydrogen bond functionalization by carbene insertion
Carmen Mart?n, Tom?s R. Belderra?n and Pedro J. P?rez
Org. Biomol. Chem., 2009, 7(22), 4777-4781

DOI:

http://dx.doi.org/10.1039/B911589G

13. Is nucleophilic cleavage chemistry practical for 4-membered heterocycles?
Harold D. Banks
Org. Biomol. Chem., 2009, 7(21), 4496-4501

DOI:

http://dx.doi.org/10.1039/B908861J

14. Synthesis and biological evaluation of the first pentafluorosulfanyl analogs of mefloquine
Peter Wipf, Tingting Mo, Steven J. Geib, Diana Caridha, Geoffrey S. Dow, Lucia Gerena, Norma Roncal and Erin E. Milner
Org. Biomol. Chem., 2009, 7(20), 4163-4165

DOI:

http://dx.doi.org/10.1039/B911483A

15. Inhibition of the exo-?-D-glucosaminidase CsxA by a glucosamine-configured castanospermine and an amino-australine analogue
Benjamin Pluvinage, Mariana G. Ghinet, Ryszard Brzezinski, Alisdair B. Boraston and Keith A. Stubbs
Org. Biomol. Chem., 2009, 7(20), 4169-4172

DOI:

http://dx.doi.org/10.1039/B913235J

16. An efficient cascade synthesis of various 2H-1,4-benzoxazin-3-(4H)-ones from o-halophenols and 2-halo-amides catalyzed by CuI
Dingben Chen, Guodong Shen and Weiliang Bao
Org. Biomol. Chem., 2009, 7(19), 4067-4073

DOI:

http://dx.doi.org/10.1039/B906210F

17. TTMPP: An efficient organocatalyst in the ring-opening of aziridines with silylated nucleophiles
Satoru Matsukawa and Kumiko Tsukamoto
Org. Biomol. Chem., 2009, 7(18), 3792-3796

DOI:

http://dx.doi.org/10.1039/B908322G

18. High-yielding synthesis of Nefopam analogues (functionalized benzoxazocines) by sequential one-pot cascade operations
Dhevalapally B. Ramachary, Vidadala V. Narayana, M. Shiva Prasad and Kinthada Ramakumar
Org. Biomol. Chem., 2009, 7(18), 3372-3378

DOI:

http://dx.doi.org/10.1039/B910397J

19. Dynamic polythioesters via ring-opening polymerization of 1,4-thiazine-2,5-diones
Yasuyuki Ura, Mohammad Al-Sayah, Javier Montenegro, John M. Beierle, Luke J. Leman and M. Reza Ghadiri
Org. Biomol. Chem., 2009, 7(14), 2878-2884

DOI:

http://dx.doi.org/10.1039/B903612A

20. Highly efficient and concise synthesis of both antipodes of SB204900, clausenamide, neoclausenamide, homoclausenamide and ?-clausenamide. Implication of biosynthetic pathways of clausena alkaloids
Luo Yang, De-Xian Wang, Qi-Yu Zheng, Jie Pan, Zhi-Tang Huang and Mei-Xiang Wang
Org. Biomol. Chem., 2009, 7(12), 2628-2634

DOI:

http://dx.doi.org/10.1039/B901965K

21. Non Lewis acid catalysed epoxide ring opening with amino acid esters
Christine Philippe, Thierry Milcent, Benoit Crousse and Dani?le Bonnet-Delpon
Org. Biomol. Chem., 2009, 7(10), 2026-2028

DOI:

http://dx.doi.org/10.1039/B902081K

22. Creative approaches towards the synthesis of 2,5-dihydro-furans, thiophenes, and pyrroles. One method does not fit all!
Matthew Brichacek and J?n T. Njardarson
Org. Biomol. Chem., 2009, 7(9), 1761-1770

DOI:

http://dx.doi.org/10.1039/B900236G

23. Intramolecular azide-alkyne [3 + 2] cycloaddition: versatile route to new heterocyclic structural scaffolds
Rongti Li, Daniel J. Jansen and Apurba Datta
Org. Biomol. Chem., 2009, 7(9), 1921-1930

DOI:

http://dx.doi.org/10.1039/B818962E

24. The synthesis of new oxazoline-containing bifunctional catalysts and their application in the addition of diethylzinc to aldehydes
Vincent Coeffard, Helge M?ller-Bunz and Patrick J. Guiry
Org. Biomol. Chem., 2009, 7(8), 1723-1734

DOI:

http://dx.doi.org/10.1039/B822580J

25. Isolation of the key intermediates in the catalyst-free conversion of oxiranes to thiiranes in water at ambient temperature
Christian M. Kleiner, Luise Horst, Christian W?rtele, Raffael Wende and Peter R. Schreiner
Org. Biomol. Chem., 2009, 7(7), 1397-1403

DOI:

http://dx.doi.org/10.1039/B820232J

26. Asymmetric recognition and sequential ring opening of 2-substituted-N-nosylaziridines with (DHQD)2AQN and TMSNu
Satoshi Minakata, Yuta Murakami, Masamitsu Satake, Ikumasa Hidaka, Yuriko Okada and Mitsuo Komatsu
Org. Biomol. Chem., 2009, 7(4), 641-643

DOI:

http://dx.doi.org/10.1039/B821650A

27. Efficient synthesis of heterocyclic compounds using ethenetricarboxylic acid diesters
Shoko Yamazaki, Yuko Iwata and Yugo Fukushima
Org. Biomol. Chem., 2009, 7(4), 655-659

DOI:

http://dx.doi.org/10.1039/B818878E

28. The use of phosphonium anhydrides for the synthesis of 2-oxazolines, 2-thiazolines and 2-dihydrooxazine under mild conditions
Maria J. Petersson, Ian D. Jenkins and Wendy A. Loughlin
Org. Biomol. Chem., 2009, 7(4), 739-746

DOI:

http://dx.doi.org/10.1039/B818310D

29. Ring-opening reaction of Bus- and SES-protected aziridines using lithiated dithianes
Ken Sakakibara and Kyoko Nozaki
Org. Biomol. Chem., 2009, 7(3), 502-507

DOI:

http://dx.doi.org/10.1039/B814413C

30. A new entry into cis-3-amino-2-methylpyrrolidines via ring expansion of 2-(2-hydroxyethyl)-3-methylaziridines
Matthias D'hooghe, Wim Aelterman and Norbert De Kimpe
Org. Biomol. Chem., 2009, 7(1), 135-141

DOI:

http://dx.doi.org/10.1039/B816617J

31. Stereoselective aziridination of cyclic allylic alcohols using chloramine-T
Susannah C. Coote, Peter O'Brien and Adrian C. Whitwood
Org. Biomol. Chem., 2008, 6(23), 4299-4314

DOI:

http://dx.doi.org/10.1039/B811137E

32. Total synthesis of siphonazole and its O-methyl derivative, structurally unusual bis-oxazole natural products
J?rg Linder, Alexander J. Blake and Christopher J. Moody
Org. Biomol. Chem., 2008, 6(21), 3908-3916

DOI:

http://dx.doi.org/10.1039/B810855B

33. Stereoselective cyclopropanation of serine- and threonine-derived oxazines to access new morpholine-based scaffolds
Filippo Sladojevich, Andrea Trabocchi and Antonio Guarna
Org. Biomol. Chem., 2008, 6(18), 3328-3336

DOI:

http://dx.doi.org/10.1039/B808895K

34. Stereoselective synthesis of (2S,3R)- and (2R,3S)-iodoreboxetine; potential SPECT imaging agents for the noradrenaline transporter
Nicola K. Jobson, Rosemary Spike, Andrew R. Crawford, Deborah Dewar, Sally L. Pimlott and Andrew Sutherland
Org. Biomol. Chem., 2008, 6(13), 2369-2376

DOI:

http://dx.doi.org/10.1039/B802819B

35. Regio- and stereocontrolled synthesis of novel 3-sulfonamido-2,3,4,5-tetrahydro-1,5-benzothiazepines from 2-(bromomethyl)- or 2-(sulfonyloxymethyl)aziridines
Michinori Karikomi, Matthias D'hooghe, Guido Verniest and Norbert De Kimpe
Org. Biomol. Chem., 2008, 6(11), 1902-1904

DOI:

http://dx.doi.org/10.1039/B804246M

36. An enantioselective approach to (+)-laurencin
Vikrant A. Adsool and Sunil V. Pansare
Org. Biomol. Chem., 2008, 6(11), 2011-2015

DOI:

http://dx.doi.org/10.1039/B803973A

37. Urea derivatives are highly active catalysts for the base-mediated generation of terminal epoxides from aldehydes and trimethylsulfonium iodide
Sarah A. Kavanagh, Alessandro Piccinini, Eimear M. Fleming and Stephen J. Connon
Org. Biomol. Chem., 2008, 6(8), 1339-1343

DOI:

http://dx.doi.org/10.1039/B719767E

38. Synthesis of carboxylic amides by ring-opening of oxazolidinones with Grignard reagents
David Bensa, Iain Coldham, Pia Fein?ugle, Ravindra B. Pathak and Roger J. Butlin
Org. Biomol. Chem., 2008, 6(8), 1401-1415

DOI:

http://dx.doi.org/10.1039/B800849C

39. Reactivity of N-(?-haloalkyl)-?-lactams with regard to lithium aluminium hydride: novel synthesis of 1-(1-aryl-3-hydroxypropyl)aziridines and 3-aryl-3-(N-propylamino)propan-1-ols
Matthias D'hooghe, Stijn Dekeukeleire and Norbert De Kimpe
Org. Biomol. Chem., 2008, 6(7), 1190-1196

DOI:

http://dx.doi.org/10.1039/B719686E

40. 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(6), 988-991

DOI:

http://dx.doi.org/10.1039/B719675J

41. Solvent control of optical resolution of 2-amino-1-phenylethanol using dehydroabietic acid
Kayoko Taniguchi, Marie Aruga, Mikio Yasutake and Takuji Hirose
Org. Biomol. Chem., 2008, 6(3), 458-463

DOI:

http://dx.doi.org/10.1039/B717071H

42. Kinetic and thermodynamic control of axial chirality in biaryl-derived fused oxazolidine lactams exploiting a centre-axis relay of unit efficiency
David J. Edwards, David House, Helen M. Sheldrake, Susan J. Stone and Timothy W. Wallace
Org. Biomol. Chem., 2007, 5(16), 2658-2669

DOI:

http://dx.doi.org/10.1039/B706336A

43. Regiochemical switching of Mitsunobu cyclisation mode of vicinal diamines with pendant hydroxyl group
James C. Anderson and Helen A. Chapman
Org. Biomol. Chem., 2007, 5(15), 2413-2422

DOI:

http://dx.doi.org/10.1039/B705081J

44. An improved methyltrioxorhenium-catalyzed epoxidation of alkenes with hydrogen peroxide
Shigekazu Yamazaki
Org. Biomol. Chem., 2007, 5(13), 2109-2113

DOI:

http://dx.doi.org/10.1039/B705276F

45. A highly efficient and general method for the ring-opening of aziridines with various nucleophiles in DMSO
Jie Wu, Xiaoyu Sun and Wei Sun
Org. Biomol. Chem., 2006, 4(22), 4231-4235

DOI:

http://dx.doi.org/10.1039/B611707D

46. Diphenylphosphinoyl chloride as a chlorinating agent – the selective double activation of 1,2-diols
David J. Fox, Daniel Sejer Pedersen, Asger B. Petersen and Stuart Warren
Org. Biomol. Chem., 2006, 4(16), 3117-3119

DOI:

http://dx.doi.org/10.1039/B606881B

47. Conformational arm-wrestling: battles for stereochemical control in benzamides bearing matched and mismatched chiral 2- and 6-substituents
Jonathan Clayden, Yann J. Y. Foricher, Madeleine Helliwell, Paul Johnson, David Mitjans and Victoria Vinader
Org. Biomol. Chem., 2006, 4(3), 444-454

DOI:

http://dx.doi.org/10.1039/B514558A

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