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The international home of synthetic, physical and biomolecular organic chemistry.
OBC Perspective Archive 2008
Chemical approach toward efficient DNA methylation analysis
Akimitsu Okamoto, Org. Biomol. Chem., 2009, 7, 21
DOI: 10.1039/b813595a
Intramolecular cyclizations of polyketide biosynthesis: mining for a 
Diels–Alderase
?
Wendy L. Kelly, Org. Biomol. Chem., 2008, 6, 4483
DOI: 10.1039/b814552k
-Acidic alkene ligand effects in Pd-catalysed cross-coupling processes: exploiting the interaction of dibenzylidene acetone (dba) and related ligands with Pd(0) and Pd(II)
Ian J. S. Fairlamb, Org. Biomol. Chem., 2008, 6, 3645
DOI: 10.1039/b811772a
Brřnsted-acid and Brřnsted-base catalyzed Diels–Alder reactions
Juan Shen and Choon-Hong Tan, Org. Biomol. Chem., 2008, 6, 3229
DOI: 10.1039/b809505c
The tert-butyl group in chemistry and biology
Philippe Bisel, Loay Al-Momani and Michael Müller, Org. Biomol. Chem., 2008, 6, 2655
DOI: 10.1039/b800083b
Bright molecules with sense, logic, numeracy and utility
A. Prasanna de Silva, Thomas P. Vance, Matthew E. S. West and Glenn D. Wright, Org. Biomol. Chem., 2008, 6, 2468
DOI: 10.1039/b802963f
Cell-penetrating peptides as delivery vehicles for biology and medicine
Kelly M. Stewart, Kristin L. Horton and Shana O. Kelley, Org. Biomol. Chem., 2008, 6, 2242
DOI: 10.1039/b719950c
Modulating the electronic properties of porphyrinoids: a voyage from the violet to the infrared regions of the electromagnetic spectrum
Yannick Rio, M. Salomé Rodríguez-Morgade and Tomás Torres, Org. Biomol. Chem., 2008, 6, 1877
DOI: 10.1039/b800617b
Catalytic addition of alkyne C–H, amine N–H, and phosphine P–H bonds to carbodiimides: an efficient route to propiolamidines, guanidines, and phosphaguanidines
Wen-Xiong Zhang and Zhaomin Hou, Org. Biomol. Chem., 2008, 6, 1720
DOI: 10.1039/b800135a
Nucleoside, nucleotide and oligonucleotide based amphiphiles: a successful marriage of nucleic acids with lipids
Arnaud Gissot, Michel Camplo, Mark W. Grinstaff and Philippe Barthélémy, Org. Biomol. Chem., 2008, 6, 1324
DOI: 10.1039/b719280k
Diversity-oriented synthesis; a spectrum of approaches and results
Richard J. Spandl, Andreas Bender and David R. Spring, Org. Biomol. Chem., 2008, 6, 1149
DOI: 10.1039/b719372f
Structure-and-mechanism-based design and discovery of therapeutics for cocaine overdose and addiction
Fang Zheng and Chang-Guo Zhan, Org. Biomol. Chem., 2008, 6, 836
DOI: 10.1039/b716268e
Thiol cofactors for selenoenzymes and their synthetic mimics
Bani Kanta Sarma and Govindasamy Mugesh, Org. Biomol. Chem., 2008, 6, 965
DOI: 10.1039/b716239a
Natural and synthetic quinones and their reduction by the quinone reductase enzyme NQO1: from synthetic organic chemistry to compounds with anticancer potential
Marie A. Colucci, Gavin D. Couch and Christopher J. Moody, Org. Biomol. Chem., 2008, 6, 637
DOI: 10.1039/b715270a
Unlocking the potential of bile acids in synthesis, supramolecular/materials chemistry and nanoscience
Nonappa and Uday Maitra, Org. Biomol. Chem., 2008, 6, 657
DOI: 10.1039/b714475j
Natural products: chemical instruments to apprehend biological symphony
Mathieu Pucheault, Org. Biomol. Chem., 2008, 6, 424
DOI: 10.1039/b713022h
The [1,
3] O-to-C rearrangement: opportunities for stereoselective synthesis
Christopher G. Nasveschuk and Tomislav Rovis, Org. Biomol. Chem., 2008, 6, 240
DOI: 10.1039/b714881j
Designer aminoglycosides: the race to develop improved antibiotics and compounds for the treatment of human genetic diseases
Mariana Hainrichson, Igor Nudelman and Timor Baasov, Org. Biomol. Chem., 2008, 6, 227
DOI: 10.1039/b712690p
Chiral recognition in noncovalent bonding interactions between helicenes: right-handed helix favors right-handed helix over left-handed helix
Ryo Amemiya and Masahiko Yamaguchi, Org. Biomol. Chem., 2008, 6, 26
DOI: 10.1039/b713700a
Molecular rearrangements through thermal [1,3] carbon shifts
John E. Baldwin and Phyllis A. Leber, Org. Biomol. Chem., 2008, 6, 36
DOI: 10.1039/b711494j
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