Akio Murai

Kindai University — Japan

Environmental Science · Physical Sciences

35h-index4.7kcitations380works0.02yr avg
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Research Topics

Marine Toxins and Detection Methods(112), Synthetic Organic Chemistry Methods(66), Marine Sponges and Natural Products(51), Oxidative Organic Chemistry Reactions(44), Carbohydrate Chemistry and Synthesis(35)

Publications380 total

Synthesis and Structure–Activity Relationship of Phosphonate Esters with (<i>S</i>)-Cinerolone and (<i>S</i>)-Jasmololone as Irreversible Inhibitors of the GDSL Esterase/Lipase TcGLIP to Study Pyrethrin Biosynthesis
ACS Omega·2025Open Access
CCDC 1517386: Experimental Crystal Structure Determination
The Cambridge Structural Database·2017Open Access
Concise Formation of Spirocyclic Compounds for Marine Phycotoxins
Heterocycles·2017· 3 citedOpen Access
Synthesis of the ABCDEF-ring of ciguatoxin 3C
Tetrahedron·2016· 6 cited
Total Synthesis of Pectenotoxin‐2
Angewandte Chemie·2013· 7 cited
Total Synthesis of Pectenotoxin‐2
Angewandte Chemie International Edition·2013· 24 citedOpen Access
Morphology of artificial snow crystals from－4 ℃ to －40 ℃ using a convection
Journal of the Japanese Society of Snow and Ice·2012· 1 citedOpen Access
Improved synthesis of C8–C20 segment of pectenotoxin-2
Tetrahedron Letters·2011· 12 cited
Water vapor measurements during snow crystal formations by the “FINEDEW” chilled mirror hygrometer
Journal of the Japanese Society of Snow and Ice·2011· 2 citedOpen Access
ChemInform Abstract: Chemical Realization of the Biogenetic Pathways Proposed for the Fused-Polycyclic Ethers of Marine Origins
ChemInform·2010
On the Shapes of Snow Crystal, and Improvement of Apparatus to Make Artificial Snow Crystals
Nihon Kikai Gakkaishi/Journal of the Japan Society of Mechanical Engineers·2009Open Access
Synthesis of the C8–C20 and C21–C30 segments of pectenotoxin 2
Tetrahedron Letters·2007· 18 cited
P-408 Stereoselective Synthesis of the Nonanomeric Spirocyclic Acetal Part of Pectenotoxin 2
International Symposium on the Chemistry of Natural Products·2006
Convergent synthesis of the common FGHI-ring part of ciguatoxins
Tetrahedron·2006· 19 cited
Synthesis of the C42—C52 Part of Ciguatoxin CTX3C.
ChemInform·2006· 1 cited
Convergent Synthesis of the IJKLM‐Ring Part of Ciguatoxin CTX3C.
ChemInform·2006
Synthesis of (+)‐Laurencin via Ring Expansion of a C‐Glycoside Derivative.
ChemInform·2005
Synthesis of the common FGHI-ring part of ciguatoxins
Tetrahedron Letters·2005· 14 cited
Convergent synthesis of the IJKLM-ring part of ciguatoxin CTX3C
Tetrahedron Letters·2005· 36 cited
Synthesis of the C42–C52 part of ciguatoxin CTX3C
Tetrahedron Letters·2005· 44 cited
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Frequent Co-authors

Kenshu Fujiwara(15), Hideshi Nakamura(11), Tadashi Masamune(7), Jun Ishihara(7), Hidetoshi Kawai(6), Takanori Suzuki(6), Naoki Kanoh(5), Akio Fukuzawa(4), Tohru Asari(4), Yasushi Ohizumi(4), Kazunori Tsushima(3), Osamu Shimomura(3), Chun Wu(3), Mitsuo Takasugi(3), Takahiro Oka(3), Mya Aye(3), Shin‐ichiro Souma(3), Yuko Ohtaniuchi(3), Hajime Matsue(3), Yoshikatsu Shimada(2)