Development of novel cyclic NGR peptide–daunomycin conjugates with dual targeting property
- Andrea Angelo Pierluigi Tripodi,
- Szilárd Tóth,
- Kata Nóra Enyedi,
- Gitta Schlosser,
- Gergely Szakács and
- Gábor Mező
Beilstein J. Org. Chem. 2018, 14, 911–918, doi:10.3762/bjoc.14.78
Local energy decomposition analysis of hydrogen-bonded dimers within a domain-based pair natural orbital coupled cluster study
- Ahmet Altun,
- Frank Neese and
- Giovanni Bistoni
Beilstein J. Org. Chem. 2018, 14, 919–929, doi:10.3762/bjoc.14.79
On the design principles of peptide–drug conjugates for targeted drug delivery to the malignant tumor site
- Eirinaios I. Vrettos,
- Gábor Mező and
- Andreas G. Tzakos
Beilstein J. Org. Chem. 2018, 14, 930–954, doi:10.3762/bjoc.14.80
Mechanochemistry of nucleosides, nucleotides and related materials
- Olga Eguaogie,
- Joseph S. Vyle,
- Patrick F. Conlon,
- Manuela A. Gîlea and
- Yipei Liang
Beilstein J. Org. Chem. 2018, 14, 955–970, doi:10.3762/bjoc.14.81
2-Iodo-N-isopropyl-5-methoxybenzamide as a highly reactive and environmentally benign catalyst for alcohol oxidation
- Takayuki Yakura,
- Tomoya Fujiwara,
- Akihiro Yamada and
- Hisanori Nambu
Beilstein J. Org. Chem. 2018, 14, 971–978, doi:10.3762/bjoc.14.82
Correlation effects and many-body interactions in water clusters
- Andreas Heßelmann
Beilstein J. Org. Chem. 2018, 14, 979–991, doi:10.3762/bjoc.14.83
Cross-coupling of dissimilar ketone enolates via enolonium species to afford non-symmetrical 1,4-diketones
- Keshaba N. Parida,
- Gulab K. Pathe,
- Shimon Maksymenko and
- Alex M. Szpilman
Beilstein J. Org. Chem. 2018, 14, 992–997, doi:10.3762/bjoc.14.84
The first Pd-catalyzed Buchwald–Hartwig aminations at C-2 or C-4 in the estrone series
- Ildikó Bacsa,
- Dávid Szemerédi,
- János Wölfling,
- Gyula Schneider,
- Lilla Fekete and
- Erzsébet Mernyák
Beilstein J. Org. Chem. 2018, 14, 998–1003, doi:10.3762/bjoc.14.85
Polysubstituted ferrocenes as tunable redox mediators
- Sven D. Waniek,
- Jan Klett,
- Christoph Förster and
- Katja Heinze
Beilstein J. Org. Chem. 2018, 14, 1004–1015, doi:10.3762/bjoc.14.86
Preparation, structure, and reactivity of bicyclic benziodazole: a new hypervalent iodine heterocycle
- Akira Yoshimura,
- Michael T. Shea,
- Cody L. Makitalo,
- Melissa E. Jarvi,
- Gregory T. Rohde,
- Akio Saito,
- Mekhman S. Yusubov and
- Viktor V. Zhdankin
Beilstein J. Org. Chem. 2018, 14, 1016–1020, doi:10.3762/bjoc.14.87
Fluorocyclisation via I(I)/I(III) catalysis: a concise route to fluorinated oxazolines
- Felix Scheidt,
- Christian Thiehoff,
- Gülay Yilmaz,
- Stephanie Meyer,
- Constantin G. Daniliuc,
- Gerald Kehr and
- Ryan Gilmour
Beilstein J. Org. Chem. 2018, 14, 1021–1027, doi:10.3762/bjoc.14.88
Hypervalent iodine-mediated Ritter-type amidation of terminal alkenes: The synthesis of isoxazoline and pyrazoline cores
- Sang Won Park,
- Soong-Hyun Kim,
- Jaeyoung Song,
- Ga Young Park,
- Darong Kim,
- Tae-Gyu Nam and
- Ki Bum Hong
Beilstein J. Org. Chem. 2018, 14, 1028–1033, doi:10.3762/bjoc.14.89
Imide arylation with aryl(TMP)iodonium tosylates
- Souradeep Basu,
- Alexander H. Sandtorv and
- David R. Stuart
Beilstein J. Org. Chem. 2018, 14, 1034–1038, doi:10.3762/bjoc.14.90
Hypervalent iodine-guided electrophilic substitution: para-selective substitution across aryl iodonium compounds with benzyl groups
- Cyrus Mowdawalla,
- Faiz Ahmed,
- Tian Li,
- Kiet Pham,
- Loma Dave,
- Grace Kim and
- I. F. Dempsey Hyatt
Beilstein J. Org. Chem. 2018, 14, 1039–1045, doi:10.3762/bjoc.14.91
Hypervalent iodine(III)-mediated decarboxylative acetoxylation at tertiary and benzylic carbon centers
- Kensuke Kiyokawa,
- Daichi Okumatsu and
- Satoshi Minakata
Beilstein J. Org. Chem. 2018, 14, 1046–1050, doi:10.3762/bjoc.14.92
An overview of recent advances in duplex DNA recognition by small molecules
- Sayantan Bhaduri,
- Nihar Ranjan and
- Dev P. Arya
Beilstein J. Org. Chem. 2018, 14, 1051–1086, doi:10.3762/bjoc.14.93
Selective carboxylation of reactive benzylic C–H bonds by a hypervalent iodine(III)/inorganic bromide oxidation system
- Toshifumi Dohi,
- Shohei Ueda,
- Kosuke Iwasaki,
- Yusuke Tsunoda,
- Koji Morimoto and
- Yasuyuki Kita
Beilstein J. Org. Chem. 2018, 14, 1087–1094, doi:10.3762/bjoc.14.94
Synthetic avenues towards a tetrasaccharide related to Streptococcus pneumonia of serotype 6A
- Aritra Chaudhury,
- Mana Mohan Mukherjee and
- Rina Ghosh
Beilstein J. Org. Chem. 2018, 14, 1095–1102, doi:10.3762/bjoc.14.95
Iodine(III)-mediated halogenations of acyclic monoterpenoids
- Laure Peilleron,
- Tatyana D. Grayfer,
- Joëlle Dubois,
- Robert H. Dodd and
- Kevin Cariou
Beilstein J. Org. Chem. 2018, 14, 1103–1111, doi:10.3762/bjoc.14.96
Recyclable hypervalent-iodine-mediated solid-phase peptide synthesis and cyclic peptide synthesis
- Dan Liu,
- Ya-Li Guo,
- Jin Qu and
- Chi Zhang
Beilstein J. Org. Chem. 2018, 14, 1112–1119, doi:10.3762/bjoc.14.97
One hundred years of benzotropone chemistry
- Arif Dastan,
- Haydar Kilic and
- Nurullah Saracoglu
Beilstein J. Org. Chem. 2018, 14, 1120–1180, doi:10.3762/bjoc.14.98
Are dispersion corrections accurate outside equilibrium? A case study on benzene
- Tim Gould,
- Erin R. Johnson and
- Sherif Abdulkader Tawfik
Beilstein J. Org. Chem. 2018, 14, 1181–1191, doi:10.3762/bjoc.14.99
Stereoselective nucleophilic addition reactions to cyclic N-acyliminium ions using the indirect cation pool method: Elucidation of stereoselectivity by spectroscopic conformational analysis and DFT calculations
- Koichi Mitsudo,
- Junya Yamamoto,
- Tomoya Akagi,
- Atsuhiro Yamashita,
- Masahiro Haisa,
- Kazuki Yoshioka,
- Hiroki Mandai,
- Koji Ueoka,
- Christian Hempel,
- Jun-ichi Yoshida and
- Seiji Suga
Beilstein J. Org. Chem. 2018, 14, 1192–1202, doi:10.3762/bjoc.14.100
