Publications by authors named "Hyung Rock Lee"

Article Synopsis
  • The muscle up (MU) is a complex gymnastics move combining a pull up and a dip, and can be done on a bar (BMU) or rings (RMU).
  • This study aimed to compare muscle recruitment in specific upper body muscles during BMU and RMU among ten active males.
  • Results showed that RMU required greater muscle activation in certain muscles (upper trapezius, biceps, and forearm flexors during pull phase; triceps and biceps during push phase), indicating that RMU is more challenging than BMU, which may be a better starting point for beginners due to its lower difficulty.
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Food-dependent exercise-induced anaphylaxis (FDEIAn) is induced by different types and various intensities of physical activity, and is distinct from food allergies. It has been shown that consumption of allergenic food followed by exercise causes FDEIAn symptoms. Intake of allergenic food or medication before exercise is a major predisposing factor for FDEIAn.

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An efficient synthetic route of L-hamamelose was successfully accomplished starting from D-ribose. L-Hamamelose was synthesized in 42% overall yield with six reaction steps via a stereoselective Grignard reaction, a stereoselective crossed aldol reaction and a controlled oxidative cleavage of the double bond of a vinyl diol compound. During the oxidative cleavage of the double bond of the vinyl diol compound with osmium tetroxide and NaIO(4), an over-oxidative cleavage of alpha-hydroxyl aldehyde generated from ring opening of the first cleaved product, formyl lactol, did not occur, probably due to the stability of the lactol form.

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Article Synopsis
  • 5''-Iodoneplanocin A was synthesized using D-ribose as the starting material.
  • This synthesis involved a series of reactions including addition-iodination-elimination, ring-closing metathesis (RCM), and oxidative rearrangement.
  • The compound is being studied for its potential use as antiviral and antitumor agents.
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Conformationally fixed bicyclo[3.1.0]hexanyl nucleosides 1 and 2 with C3'-ethenyl group were successfully synthesized and evaluated against various viruses.

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Synthesis of novel cyclopropyl pyrimidine and purine nucleoside derivatives was successfully achieved using one pot reactions including an alkylation, an oxirane-ring opening reaction and a lactonization and a hydroboration-oxidation as the key steps in order to find new antiherpetic agent.

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Article Synopsis
  • N-hydroxycytosine nucleoside 3 was created as a potential treatment for Hepatitis C Virus (HCV).
  • The synthesis process began with D-ribose and involved several key reactions, including an iodine-fluorine exchange, RCM reaction, stereoselective reduction, and Mitsunobu reaction.
  • BuLi (butyllithium) was utilized as a crucial reagent in the synthesis steps.
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