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Featured researches published by Akihiko Matsuo.


Cellular and Molecular Life Sciences | 1974

(−)-Maalioxide and (+)-cyclocolorenone, enantiomeric sesquiterpenoids from the liverwort, Plagiochila acanthophylla subsp. japonica

Akihiko Matsuo; Mitsuru Nakayama; S. Sato; Tetsuo Nakamoto; Seiryu Uto; Shûichi Hayashi

Aus den Hexanextrakten vonPlagiochila acanthophylla subsp.japonica wurden (−)-Maalioxid und (+)-Cyclocolorenon isoliert. Diese Verbindungen sind enantromer zu denjenigen, die aus höheren Pflanzen erhalten worden sind.


Phytochemistry | 1985

Enantiomeric type sesquiterpenoids of the liverwort Marchantia polymorpha

Akihiko Matsuo; Nobuyuki Nakayama; Mitsuru Nakayama

Abstract A series of ent -sesquiterpenoids corresponding to the optical antipodes of those in higher plants have been isolated from the liverwort Marchantia polymorpha . These sesquiterpenoids provide yet another example of the peculiar stereospecificity of the biogenesis of the liverwort sesquiterpenoids and suggest a special taxonomic position of the liverworts in the plant kingdom.


Phytochemistry | 1975

Enantiomeric cuparene-type sesquiterpenoids from Bazzania pompeana

Akihiko Matsuo; Mitsuru Nakayama; T. Maeda; Y. Noda; Shûichi Hayashi

Abstract Two enantiomeric cuparene-type sesquiterpenoids, (R)-(−)-cuparene ( 1 ) and (R)-(−)-δ-cuparenol ( 2 ), have been isolated from the liverwort, Bazzania pompeana . The structures and absolute configurations of the two compounds have been determined.


Cellular and Molecular Life Sciences | 1969

Bazzanene, a sesquiterpene hydrocarbon of a new carbon skeleton fromBazzania pompeana (Lac.) Mitt.

Shûichi Hayashi; Akihiko Matsuo; Tamon Matsuura

Aus dem essentiellen öl vonBazzania pompeana (Lac.) Mitt. wurde Bazzanen, ein Sesquiterpen-Kohlenwasserstoff mit einem neuartigen Kohlenstoffgerüst, isoliert. Bazzanen besitzt die Struktur des 2,6,6-Trimethyl-8-methylen bicyclo[5.3.1.]undec-2-ens.


Tetrahedron Letters | 1980

Labdane diterpene glycosides with 6-deoxy-L-idose from Aster spathulifolius Maxim.

Yasuto Uchio; M. Nagasaki; Shizuko Eguchi; Akihiko Matsuo; Mitsuru Nakayama; Shûichi Hayashi

Abstract Three labdane type diterpene glycosides ( 1 , 2 and 3 ) with 6-deoxy-L-idose have been isolated from Aster spathulifolius Maxim. and their structures have been determined on the basis of chemical and spectral data.


Cellular and Molecular Life Sciences | 1970

Bazzanenol, a new sesquiterpene alcohol having a skeleton of Bicyclo[5.3.1] undecane system from hepaticae,Bazzania pompeana (Lac.) Mitt

Shûichi Hayashi; Akihiko Matsuo

Isolierung und Strukturaufklärung eines neuen Sesquiterpenalkohols ausBazzania pompeana (Lac.) Mitt.


Phytochemistry | 1988

Dolabellane diterpenoids from the liverwort Odontoschisma denudatum

Akihiko Matsuo; Ki-ichiro Kamio; Katsumi Uohama; Ken-ichiro Yoshida; George A. Sim

Abstract Five new dolabellane diterpenoids have been isolated from the liverwort Odontoschisma denudatum, and their structures and absolute configurations have been determined on the basis of 1H and 13C NMR evidence and chemical correlation.


Cellular and Molecular Life Sciences | 1979

(−)-Maalian-5-ol, a new enantiomeric sesquiterpenoid from the liverwortPlagiochila ovalifolia

Akihiko Matsuo; Hiroshi Nozaki; H. Kataoka; Mitsuru Nakayama; Shûichi Hayashi

A new enantiomeric sesquiterpene alcohol named (−)-maalian-5-ol was isolated from the liverwort, and the structure and absolute configuration was determined to be the stereostructureI by chemical and spectral evidence.


Phytochemistry | 1980

Fatty acid ethyl esters in the liverwort conocephalum conicum

Akihiko Matsuo; Mitsuru Nakayama; Shŭichi Hayashi; Kimiko Nagai

Abstract A series of fatty acid ethyl esters ranging from C 14 to C 24 was isolated from a hexane extract of the liverwort Conocephalum conicum , these esters accounted for 77% of the extract. The ethyl esters consisting of even-numbered fatty acids were predominant and ethyl palmitate was the major constituent.


Cellular and Molecular Life Sciences | 1977

(-)-Dihydromylione A, a novel tetracyclic sesquiterpene ketone containing two conjugated cyclopropane rings, from Mylia taylorii (liverwort)

Akihiko Matsuo; Hiroshi Nozaki; M. Shigemori; Mitsuru Nakayama; Shûichi Hayashi

A novel tetracyclic sesquiterpene ketone named (-)-dihydromylione A (III) was isolated from the liverwort, and the structure was determined together with the absolute configuration to be ent-5, 10-cyclo-aromadendr-3-one by connecting the compound with co-occurring (-)-myliol (II).

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