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Dive into the research topics where Mugio Nishizawa is active.

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Featured researches published by Mugio Nishizawa.


Tetrahedron Letters | 1983

A new olefin cyclization agent, mercury(II) trifluoremethanesulfonate—amine complex

Mugio Nishizawa; Hideyuki Takenaka; Hisaya Nishide; Yuji Hayashi

Abstract A new reagent, mercury(II) trifluoromethanesulfonate—amine complex, has been developed for effective cyclization of various farnesol derivatives in good yield and high selectivity.


Phytochemistry | 1983

(+)-8-Hydroxycalamenene: a fish-poison principle of Dysoxylum acutangulum and D. alliaceum

Mugio Nishizawa; Akio Inoue; Setijati Sastrapradja; Yuji Hayashi

Abstract A fish-poison principle of Dysoxylum acutangulum and D. alliaceum has been identified as (+)-8-hydroxycalamenene, a new natural sesquiterpene phenol. This compound shows not only significant toxicity against fish but also antibacterial activity.


Phytochemistry | 1990

Malonate half-esters of homolanostanoid from an asian Ganoderma fungus

Chairul; Takashi Tokuyama; Mugio Nishizawa; Motoo Shiro; Harukuni Tokuda; Yuji Hayashiji

Abstract From the fruit body of an Indonesian Ganoderma species (Polyporaceae), malonic acid half-esters of two new homolanostanoid triterpene hydroxyacids have been isolated along with carboxyacetylquercinic acid, and characterized as their methyl esters. The stereochemistry of carboxyacetylquercinic acid was established by the X-ray crystallography of its methyl ester, and the structures of the two new components were determined by spectral analysis and comparisons with the methyl ester of carboxyacetylquercinic acid. An anti-tumour promoting activity of these quercinic acid derivatives is also reported.


Tetrahedron Letters | 1982

The structure of Lansioside A : A novel triterpene glycoside with amino-sugar from lansium domesticum

Mugio Nishizawa; Hisaya Nishide; Yuji Hayashi; Soleh Kosela

Abstract Lansioside A, a novel triterpene amino-sugar glycoside, is isolated from Lansium domesticum and its full structure including absolute configuration is established by the chemical derivation and spectral study.


Tetrahedron Letters | 1986

Biomimetic cyclization of ambliofuran and analog by using mercury(II) triflate/N,N-dimethylanilline complex: Synthesis of (±) -Ambliol-A

Mugio Nishizawa; Hidetoshi Yamada; Yuji Hayashi

Abstract Biomimetic cyclization of ambliofuran with mercury(II) triflate/N,N-dimethylaniline complex is initiated from the internal double bond (Δ7) in high selectivity, whereas the corresponding sulfone is cyclized from terminal (Δ15) olefin to give marginatan skeleton.


Tetrahedron Letters | 1986

Total synthesis of (±) Baiyunol

Mugio Nishizawa; Hidetoshi Yamada; Yuji Hayashi

Abstract On the basis of highly efficient cationic cyclazation of 13-oxoambliofuran with mercury(II) triflate/ N , N -dimethylaniline complex, the first total synthesis of (±)-baiyunol, an aglycon of a sweet substance. Is accomplished in a short-step sequence.


Tetrahedron Letters | 1984

Total synthesis of (±)-α,γ-onoceradienedione and lansic acid

Mugio Nishizawa; Hisaya Nishide; Yuji Hayashi

Abstract Unsymmetrical onoceranoid triterpenes,α,γ-onoceradienedione and lansic acid, have been synthesized effectively by means of mercury(II) triflate/amine complex-induced olefin cyclization.


Tetrahedron | 1977

STUDIES ON THE SESQUITERPENOIDS OF HYPOLEPIS PUNCTATA METT. II

Yuji Hayashi; Mugio Nishizawa; Takeo Sakan

Abstract Hypacrone ( 1 ), a new seco-illudoid sesquiterpene, was isolated from a fern, Hypolepis punctata Mett., as its characteristic acrid principle. The structure is proposed on the spectral basis and the transformation into pterosins, illudoid constituents of the same plant.


Phytochemistry | 1983

Isolation of individual type II cyanolipids from Nephelium lappaceum

Mugio Nishizawa; Kenji Adachi; Setijati Sastrapradja; Yuji Hayashi

Abstract Three kinds of type II cyanolipids were isolated as pure forms from Nephelium lappaceum using HPLC. The full structures were established by spectral and chemical investigations.


Tetrahedron | 1977

Studies on the sesquiterpenoids of hypolepis punctata mett.—II : The total synthesis of hypacrone

Yuji Hayashi; Mugio Nishizawa; Takeo Sakan

Hypacrone (1), a new seco-illudoid, was synthesized by several steps, including a cross aldol condensation of two major moieties, a diketone (2) and a cyclopentenone derivative (11).

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Hidetoshi Yamada

Tokushima Bunri University

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Chairul

Osaka City University

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