1)
Activity-Based Probes That Target Functional Subclasses of Phospholipases in Proteomes
Sarah E. Tully and Benjamin F. Cravatt
J. Am. Chem. Soc., 2010, 132 (10), pp 3264–3265
Код: Выделить всё
dx.doi.org/10.1021/ja1000505A Modular Synthesis of Alkynyl-Phosphocholine Headgroups for Labeling Sphingomyelin and Phosphatidylcholine
Mahendra S. Sandbhor, Jessie A. Key, Ileana S. Strelkov and Christopher W. Cairo
J. Org. Chem., 2009, 74 (22), pp 8669–8674
Код: Выделить всё
dx.doi.org/10.1021/jo901824hBio-orthogonal Phosphatidylserine Conjugates for Delivery and Imaging Applications
Andrew J. Lampkins, Edward J. O’Neil and Bradley D. Smith
J. Org. Chem., 2008, 73 (16), pp 6053–6058
Код: Выделить всё
dx.doi.org/10.1021/jo8011336Synthesis and Evaluation of 1,2,3-Triazole Containing Analogues of the Immunostimulant α-GalCer
Taeho Lee, Minjae Cho, Sung-Youl Ko, Hyun-Jun Youn, Dong Jae Baek, Won-Jea Cho, Chang-Yuil Kang, and Sanghee Kim
J. Med. Chem., 2007, 50 (3), pp 585–589
Код: Выделить всё
dx.doi.org/10.1021/jm061243qPhosphatidylcholine-Derived Bolaamphiphiles via Click Chemistry
Edward J. O'Neil, Kristy M. DiVittorio, and Bradley D. Smith
Org. Lett., 2007, 9 (2), pp 199–202
Код: Выделить всё
dx.doi.org/10.1021/ol062557aSynthesis and Spectral Properties of Cholesterol- and FTY720-Containing Boron Dipyrromethene Dyes
Zaiguo Li and Robert Bittman
J. Org. Chem., 2007, 72 (22), pp 8376–8382
Код: Выделить всё
dx.doi.org/10.1021/jo701475qSynthesis of Borondipyrromethene (BODIPY)-Labeled Sphingosine Derivatives by Cross-metathesis Reaction
Carsten Peters, Andreas Billich, Michael Ghobrial, Klemens Högenauer, Thomas Ullrich, and Peter Nussbaumer
J. Org. Chem., 2007, 72 (5), pp 1842–1845
Код: Выделить всё
dx.doi.org/10.1021/jo062347b