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Synthesis of sterically-hindered 1,7-dicarba-closo-dodecarborane thiourea analogs
- Authors
- Choi, Seunghyun; Byun, Youngjoo
- Issue Date
- 1-6월-2013
- Publisher
- ELSEVIER SCIENCE SA
- Keywords
- Carborane; Isothiocyanate; Thiourea; Conjugation
- Citation
- JOURNAL OF ORGANOMETALLIC CHEMISTRY, v.733, pp.49 - 52
- Indexed
- SCIE
SCOPUS
- Journal Title
- JOURNAL OF ORGANOMETALLIC CHEMISTRY
- Volume
- 733
- Start Page
- 49
- End Page
- 52
- ISSN
- 0022-328X
- Abstract
- We herein report the first successful synthesis of 1-thioisocyanato-1,7-dicarba-closo-dodecarborane, which afforded novel lipophilic thiourea analogs by reacting with weak and bulky nucleophilic amines including 1-adamantylamine, and m-carboranylamine, aniline, and 2-aminopyridine. Newly synthesized thiourea analogs were fully characterized by NMR, ESI-MS, and FTIR. (C) 2013 Elsevier B.V. All rights reserved.
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Collections - College of Pharmacy > Department of Pharmaceutical Science > 1. Journal Articles
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