Papers - Nishiyama, Shigeru

よりクリーンな有機合成反応を目指して.

NISHIYAMA SHIGERU

化学 (化学同人)  62 ( 8 ) 66-67 2007.08

Research paper (scientific journal), Single Work, Accepted

新規生物活性物質を目指す有機電解合成

NISHIYAMA SHIGERU

化学と生物 (学会出版センター)  45 ( 3 ) 191-196 2007.03

Research paper (scientific journal), Single Work, Accepted

Asymmetric synthesis of the polyol subunit of the macrolide antibiotic, ossamycin: a unique approach utilizing stereochemical specificity.

N. Kutsumura and S. Nishiyama

Bull. Chem. Soc. Jpn. 79 ( 3 ) 468 － 478 2007.03

Research paper (scientific journal), Joint Work, Accepted

リグナン、ネオリグナン天然物化学ー植物編ー（山村庄亮、長谷川宏司編）

NISHIYAMA SHIGERU

天然物化学ー植物編ー（山村庄亮、長谷川宏司編） (アイピーシー出版部)     341-349 2007

Research paper (conference, symposium, etc.), Joint Work, Accepted

Synthesis of chloroquinocin, a pyranonaphthoquinone antibiotic against Gram-positive bacteria.

A. Shimbashi and S. Nishiyama

Tetrahedron Lett. 48 ( 9 ) 1545-1548 2007

Research paper (scientific journal), Joint Work, Accepted

Synthesis of pinguisane-type sesquiterpenoids, acutifolone a, and pinguisenol, along with bisacutifolones through the Diels-Alder Dimerization reaction.

NISHIYAMA SHIGERU

Eur. J. Org. Chem.  ( 31 ) 5190-5197 2007

Research paper (scientific journal), Joint Work, Accepted

　View Summary

The total synthesis of pinguisane-type sesquiterpenoids, acutifolone
A (1) and pinguisenol (2), has been achieved by
using the Mukaiyama aldol reaction as the key step. The
intermolecular Diels–Alder reaction of these monomeric natural
products successfully led to stereoselective dimerization,
leading to bisacutifolones A (3) and B (4). Theoretical calculations
revealed that the dimerization reaction proceeded
through the most stable transition state.

08010333052320080317172538PDF1.pdf

An efficient synthesis of propargylic ethers under the DBU conditions and its application to natural products synthesis.

T. Yokoyama, N. Kutsumura, T. Ohgiya, and S. Nishiyama

Bull. Chem. Soc. Jpn. 80 ( 37 ) 578-582 2006.03

Research paper (scientific journal), Single Work

Total synthesis, structural revision and biological evaluation of calafianin, a marine spiroisoxazoline from the sponge, Aplysina gerardogreeni.

T. Ogamino, R. Obata, H. Tomoda, and S. Nishiyama

Bull. Chem. Soc. Jpn. 79 ( 1 ) 134-139 2006.01

Research paper (scientific journal), Joint Work, Accepted

Oxidative cyclization of isodityrosine tripeptides with electrochemically generated thallium(III) ion.

T. Tanabe, R. Obata, and S. Nishiyama

HETEROCYCLES 69   113-118 2006

Research paper (scientific journal), Single Work, Accepted

Asymmetric synthesis of aerothionin, a marine dimeric spiroisoxazoline natural product, employing optically active spiroisoxazoline derivative.

T. Ogamino, R. Obata and S. Nishiyama

Tetrahedron Lett. 47 ( 5 ) 727-731 2006

Research paper (scientific journal), Joint Work, Accepted

Synthesis of verbenachalcone congeners and their biological assessment against activation of the NGF-mediated neurite outgrowth of PC12D cells activity.

T. Tanabe, T. Ogamino, Y. Shimizu, M. Imoto, and S. Nishiyama

Bioorg. Med. Chem. 14 ( 8 ) 2753 － 2762 2006

Research paper (scientific journal), Joint Work, Accepted

Synthesis and biological assessment of hemiacetal spiro derivatives towards development of efficient chemotherapeutic agent.

T. Ogamino, S. Ohnishi, Y. Ishikawa, R. Obata, and S. Nishiyama

STAM 7 ( 2 ) 175-183 2006

Research paper (scientific journal), Joint Work, Accepted

Synthesis of chiloscyphones and biological activities of their synthetic intermediates against methicillin-resistant Staphylococcus aureus (MRSA).

J. Shiina, R. Obata, H. Tomoda, and S. Nishiyama

Eur. J. Org. Chem.  ( 10 ) 2363-2370 2006

Research paper (scientific journal), Joint Work, Accepted

1,2-Dibromoalkanes into alkynes by elimination reaction under DBU conditions and its application to total synthesis of sapinofuranone B.

N. Kutsumura, T. Yokoyama, T. Ohgiya, and S. Nishiyama

Tetrahedron Lett. 47 ( 25 ) 4133-4136 2006

Research paper (scientific journal), Single Work, Accepted

Solid-phase synthesis and biological activities of biphenyl ether-containing cyclic oligopeptides.

K. Nakamura, R. Obata, and S. Nishiyama

Peptide Science 2005, The Japanese peptide Society    127-130 2006

Research paper (scientific journal), Joint Work, Accepted

Oxidation of mangostins, the naturally occurring xanthone derivatives carrying diverse biological activities.

Y. Nishihama, Y. Amano, T. Ogamino, and S. Nishiyama

Electrochemistry 74 ( 8 ) 609-611 2006

Research paper (scientific journal), Joint Work, Accepted

Synthetic studies of N-demethylossamine and elaboration of its glycosylation.

N. Kutsumura and S. Nishiyama

J. Carbohydr. Chem. 25   377-385 2006

Research paper (scientific journal), Joint Work, Accepted

Oxidative synthesis of azacyclic derivatives through the nitrenium ion: application of a hypervalent iodine species electrochemically generated from iodobenzene.

Y. Amano and S. Nishiyama

Tetrahedron Lett. 47 ( 37 ) 6505-6507 2006

Research paper (scientific journal), Joint Work, Accepted

Total synthesis of (+)-tanikolide, using regioselective elimination of a vicinal dibromoalkane.

T. Ohgiya, K. Nakamura, and S. Nishiyama,

Bull. Chem. Soc. Jpn. 78 ( 8 ) 1549-1554 2005.08

Research paper (scientific journal), Joint Work, Accepted

フェニルピルビン酸オキシムを基本骨格とする海洋生物由来の生物活性物質の化学.

NISHIYAMA SHIGERU

有機合成化学協会誌 63 ( 6 ) 583-593 2005.06

Research paper (scientific journal), Single Work