[1]OrganicLetters,2002,vol.4,p.4139-4142
[2]JournalofOrganicChemistry,1991,vol.56,p.893-896
[1]JournalofOrganicChemistry,1991,vol.56,p.893-896
[2]Tetrahedron,1993,vol.49,p.1725-1738
[3]SyntheticCommunications,1998,vol.28,p.99-108
[4]JournalofOrganicChemistry,1999,vol.64,p.8794-8800
[1]JournaloftheChemicalSociety.Chemicalcommunications,1995,p.301-302
[2]Patent:EP907663,2004,B1.Locationinpatent:Page8;10;12
[3]Patent:WO2009/109792,2009,A1.Locationinpatent:Page/Pagecolumn16
[4]Patent:WO2009/109792,2009,A1.Locationinpatent:Page/Pagecolumn17-18
[5]Patent:US2004/260081,2004,A1.Locationinpatent:Page/Pagecolumn7-8
[6]Patent:US2004/260081,2004,A1.Locationinpatent:Page/Pagecolumn7-8
[7]Patent:US2004/260081,2004,A1.Locationinpatent:Page/Pagecolumn7-8
[8]Patent:EP1498404,2005,A1.Locationinpatent:Page/Pagecolumn7-8
[9]Patent:EP1498404,2005,A1.Locationinpatent:Page/Pagecolumn7-9
[10]Patent:US7683167,2010,B2.Locationinpatent:Page/Pagecolumn7;8;9
[11]Patent:US2009/124798,2009,A1.Locationinpatent:Page/Pagecolumn9;11
[12]Patent:US2009/124798,2009,A1.Locationinpatent:Page/Pagecolumn10-11
[13]Patent:US2009/124798,2009,A1.Locationinpatent:Page/Pagecolumn9-11
[14]Patent:US2009/124798,2009,A1.Locationinpatent:Page/Pagecolumn11
[15]Chirality,2012,vol.24,p.329-338
[16]AsianJournalofChemistry,2012,vol.24,p.4917-4922
[17]Chirality,2013,vol.25,p.54-58
[18]BulletinoftheKoreanChemicalSociety,2013,vol.34,p.2623-2628
[19]Chirality,2015,vol.27,p.518-522
[20]Chirality,2015,vol.27,p.507-517
[21]Chirality,2015,vol.27,p.500-506
[22]ChemistryLetters,2015,vol.44,p.946-948
[23]ChemistryLetters,2015,vol.44,p.1479-1481
[24]Chirality,2016,vol.28,p.340-346
[25]Molecules,2016,vol.21
[26]Molecules,2016,vol.21
[27]Molecules,2016,vol.21
[28]ChemicalCommunications,2017,vol.53,p.509-512
[29]Chirality,2017,vol.29,p.430-442
[30]Chirality,2017,vol.29,p.512-521
[31]Chirality,2018,vol.30,p.74-84
[32]BulletinoftheKoreanChemicalSociety,2019,vol.40,p.146-149
[33]JournaloftheAmericanChemicalSociety,2019
[1]BulletinoftheChemicalSocietyofJapan,1996,vol.69,p.1755-1761
[1]TetrahedronAsymmetry,2001,vol.12,p.1737-1740
Title: Chemical profiling of the cytotoxic triterpenoid-concentrating fraction and characterization of ergostane stereo-isomer ingredients from Antrodia camphorata.
Journal: Journal of pharmaceutical and biomedical analysis 20120125
Title: Phosphorus-nitrogen compounds. 21. Syntheses, structural investigations, biological activities, and DNA interactions of new N/O spirocyclic phosphazene derivatives. The NMR behaviors of chiral phosphazenes with stereogenic centers upon the addition of chiral solvating agents.
Journal: Inorganic chemistry 20100802
Title: Phosphorus-nitrogen compounds. 18. Syntheses, stereogenic properties, structural and electrochemical investigations, biological activities, and DNA interactions of new spirocyclic mono- and bisferrocenylphosphazene derivatives.
Journal: Inorganic chemistry 20091102
Title: The structural and stereogenic properties of pentaerythritoxy-bridged cyclotriphosphazene derivatives: spiro-spiro, spiro-ansa and ansa-ansa isomers.
Journal: Dalton transactions (Cambridge, England : 2003) 20060314