K. Naemura

发表

Temperature dependent inversion of enantiomer selectivity in thecomplexation of optically active azophenolic crown ethers containingalkyl substituents as chiral barriers with chiralamines1

Keiji Hirose, Y. Tobe, Junichi Fuji, 1997 .

Temperature Dependence of Enantioselectivity in Complexations of Optically Active Phenolic Crown Ethers with Chiral Amines in Solution

Keiji Hirose, Y. Tobe, Junichi Fuji, 1998 .

Enantioselective complexation of phenolic crown ethers with chiral aminoethanol derivatives: effects of substituents of aromatic rings of hosts and guests on complexation

Keiji Hirose, Y. Tobe, K. Naemura, 2000 .

Chiral molecular recognition in electrospray ionization mass spectrometry

H. Doe, R. Arakawa, T. Matsuo, 1996 .

Preparation of homochiral phenolic crown ether having chiral subunits derived from (1R,2S)-cis-1,2,3,4-tetrahydronaphthalene-1,2-diol: temperature-dependent enantioselectivity in complexations with neutral amines

Keiji Hirose, Y. Tobe, K. Naemura, 1997 .

Enzyme-Catalyzed Enantioselective and Regioselective Hydrolyses of (2RS,7SR)-2,7-Diacetoxybicyclo[2.2.1]heptane and (2RS,7RS)-2,7-Diacetoxybicydo[2.2.1]heptane

N. Takahashi, K. Naemura, H. Chikamatsu, 1990 .

Absolute Configuration of Optically Active Tricyclo[2.2.1.02,6]heptan-3-ol (Nortricyclanol). An Enhancement of Enantiomeric Purity of a Chiral Alcohol by Repeating Enzymatic Kinetic Resolution

K. Naemura, H. Chikamatsu, M. Saitoh, 1989 .

Facile Preparation of Optically Active Bicyclo[3.3.1]nonane-2,6-diol and 3,3,7,7-Tetramethylbicyclo[3.3.1]nonane-2,6-diol by Enzyme-Catalyzed Hydrolysis, and Enantiomer Recognition Behavior of Crown Ethers and Podands Having These Diols as a Chiral Subunit

M. Komatsu, K. Naemura, H. Chikamatsu, 1989 .

Enzyme-catalyzed Asymmetric Hydrolysis of meso-Substrate. The Facile Synthesis of Both Enantiomers of cis-2,5-Disubstituted Tetrahydrofuran Derivatives

N. Takahashi, K. Naemura, H. Chikamatsu, 1988 .

Stereochemistry of Twisted Double Bond Systems

Koji Yamamoto, M. Nakazaki, K. Naemura, 1985, Stereochemistry.

Synthesis and self-association properties of diethynylbenzene macrocycles

Y. Tobe, N. Utsumi, K. Naemura, 1996 .

m-Diethynylbenzene macrocycles: syntheses and self-association behavior in solution.

Keiji Hirose, Y. Tobe, M. Sonoda, 2002, Journal of the American Chemical Society.

Synthesis and Association Behavior of [4.4.4.4.4.4]Metacyclophanedodecayne Derivatives with Interior Binding Groups.

Y. Tobe, N. Utsumi, K. Naemura, 1998, Angewandte Chemie.

Diels−Alder Reactions of Tetraethynylcyclopentadienones. An Approach to Differentially Substituted Hexaethynylbenzenes of C2v Symmetry

Y. Tobe, K. Naemura, K. Kubota, 1997 .

Synthesis of butadiyne-bridged [4n] metacyclophanes having exo-annular t-butyl groups

Y. Tobe, M. Sonoda, N. Utsumi, 2001 .

Lipase-catalyzed enantioselective acylation of alcohols: a predictive active site model for lipase YS to identify which enantiomer of an alcohol reacts faster in this acylation

Keiji Hirose, Y. Tobe, M. Konishi, 1995 .

Lipase YS-catalysed acylation of alcohols: a predictive active site model for lipase YS to identify which enantiomer of a primary or a secondary alcohol reacts faster in this acylation

Keiji Hirose, Y. Tobe, M. Konishi, 1994 .

Enzyme-catalyzed asymmetric acylation and hydrolysis of cis-2,5-disubstituted tetrahydrofuran derivatives: Contribution to development of models for reactions catalyzed by porcine liver esterase and porcine pancreatic lipase

Y. Tobe, N. Takahashi, Y. Hirose, 1993 .

Resolution of the diols of bicyclo[2.2.1]heptane, bicyclo[2.2.2]octane and bicyclo[3.2.1]octane by enzymic hydrolysis, and their absolute configurations

N. Takahashi, K. Naemura, Shunsuke Tanaka, 1992 .

Enzyme-catalysed asymmetric synthesis of a spiro[3.3]heptane derivative with axial chirality and enzymatic resolution of racemic spiro[3.3]heptane derivatives

K. Naemura, A. Furutani, 1990 .

C2-ketone rule in horse liver alcohol dehydrogenase (HLADH) mediated oxidoreduction

Yasuyuki Sasaki, M. Nakazaki, K. Naemura, 1981 .

Microbial stereo-differentiating reduction of carbonyl compounds; proposed quadrant rule

M. Asao, Toru Shimizu, M. Nakazaki, 1980 .

Microbial stereo-differentiating reduction of the carbonyl groups located on the C2 axes of gyrochiral molecules

M. Asao, M. Nishino, M. Nakazaki, 1979 .

Novel Self-Assembly of m-Xylylene Type Dithioureas by Head-to-Tail Hydrogen Bonding.

Keiji Hirose, Y. Tobe, K. Naemura, 1997, The Journal of organic chemistry.

Synthesis of the D2d-dinoradamantane derivatives having two coaxially oriented unsaturated centers. 6-Methylene-D2d-dinoradamantan-2-one and D2d-dinoradamantane-2,6-dione

H. Harada, M. Nakazaki, K. Naemura, 1982 .

Synthesis and absolute configuration of optically active D3-tritwistane; the gyrochiral prototype of "twist" diamond

M. Nakazaki, M. Hashimoto, K. Naemura, 1981 .

GENERATION OF CYCLOCARBONS WITH 4N CARBON ATOMS (C12, C16 AND C20) BY 2 + 2 CYCLOREVERSION OF PROPELLANE-ANNELATED DEHYDROANNULENES

Y. Achiba, Y. Tobe, Tomonari Wakabayashi, 1996 .

A New Entry into Cyclo[n]carbons: [2 + 2] Cycloreversion of Propellane-Annelated Dehydroannulenes

Y. Achiba, Y. Tobe, Tomonari Wakabayashi, 1996 .

Towards the synthesis of monocyclic carbon clusters: [2+2] cycloreversion of propellane annelated dehydroannulenes

Y. Tobe, K. Naemura, H. Matsumoto, 1996 .

Photochemical Method for Generation of Linear Polyynes: [2 + 2] Cycloreversion of [4.3.2]Propellatrienes Extruding Indan

Y. Tobe, K. Naemura, T. Fujii, 1994 .

Improvement of enantioselectivity in kinetic resolution of a primary alcohol through lipase-catalyzed transesterification by using a chiral acyl donor

Keiji Hirose, Y. Tobe, K. Naemura, 2000 .

Enantioselective acylation of primary and secondary alcohols catalyzed by lipase QL from Alcaligenes sp.: A predictive active site model for lipase QL to identify which enantiomer of an alcohol reacts faster in this acylation

Keiji Hirose, Y. Tobe, K. Naemura, 1996 .

The synthesis and the absolute configuration of optically active tricyclo[4.4.0.03.8]decane

K. Adachi, M. Nakazaki, K. Naemura, 1968 .

Synthesis of the first optically active anti-Bredt-rule compound with known absolute configuration. (-)-(S)-Bicyclo[3.3.1]-1(2)-nonene

M. Nakazaki, K. Naemura, S. Nakahara, 1979 .

Synthesis of the first optically active anti-Bredt rule compound with known absolute configuration: (–)-(5S)-bicyclo[3.3.1]non-1-ene

M. Nakazaki, K. Naemura, S. Nakahara, 1979 .

Synthesis and Structure of (6)(1,4)Naphthalenophane and (6)(1,4)Anthracenophane and Their Peri-Substituted Derivatives.

Y. Tobe, K. Naemura, Shinji Saiki, 1997 .

Regioselective metalation of [6]paracyclophane with a superbase

K. Kakiuchi, Y. Tobe, K. Naemura, 1993 .

Enantioselective acylation of alcohols catalyzed by lipase QL from Alcaligenes sp.: A predictive active site model for lipase QL to identify the faster reacting enantiomer of an alcohol in this acylation

Keiji Hirose, Y. Tobe, K. Naemura, 1996 .

Synthesis and Properties of Chiral Macrobicyclic and Macrotricyclic Cryptands Containing the trans-Tetrahydrofuran-2,5-diylbis(methylene) Subunit as the Chiral Center

K. Naemura, Y. Kanda, H. Chikamatsu, 1987 .

SYNTHESIS OF NOVEL CROWN ETHER INCORPORATING THE (−)-(5S,6R,13S,14R)-5,6,13,14-TETRAHYDRO-5,13-METHANOCYCLOOCTA[1,2-a:5,6-a′]DINAPHTHALENE-6,14-DIOL SUBUNIT AS THE C2-SYMMETRIC CHIRAL CENTER

K. Naemura, R. Fukunaga, 1985 .

Optical Activity and Absolute Configuration of 2,3 :6,7-Dibenzobicyclo [3.3.1]nona-2,6-diene Derivatives

Y. Nakagawa, M. Nakazaki, K. Naemura, 1975 .

Chiral amino acid recognition detected by electrospray ionization (ESI) and fast atom bombardment (FAB) mass spectrometry (MS) coupled with the enantiomer-labelled (EL) guest method

Takahiro Kaneda, Masami Sawada, Keiji Hirose, 1998 .

Chiral recognition in molecular complexation for the crown ether–amino ester system. A facile FAB mass spectrometric approach

Keiji Hirose, Y. Tobe, M. Sawada, 1994 .

[2 + 2] Cycloreversion of [4.3.2]Propella-1,3,11-trienes: An Approach to Cyclo[n]carbons from Propellane-Annelated Dehydro[n]annulenes

Y. Tobe, M. Sonoda, Tomonari Wakabayashi, 2000 .

Preparation and Chiroptical Properties of Optically Active Tetracyclic Cage-shaped Hydrocarbons; [m.0]Triblattanes and [m.1]Triblattanes

M. Nakazaki, K. Naemura, H. Chikamatsu, 1985 .

The preparation and chiroptical properties of cage-shaped pentacyclic hydrocarbons; (m.n.0)Triblattanes. Horse liver alcohol dehydrogenase mediated reduction of pentacyclo(5.5.0.02,6.03,9.05,8)dodecan-4-one.

M. Nakazaki, K. Naemura, H. Chikamatsu, 1984 .

Diazomethane ring-expansion of (-)-D3-trishomocubanone. Preparation and chiroptical properties of a series of (m.1.1)triblattanes.

M. Nakazaki, M. Hashimoto, K. Naemura, 1983 .

Unusual consecutive rearrangements in the Demjanov ring-expansion reaction of 2-(aminomethyl)-D2d-dinoradamantane and 9-(aminomethyl)noradamantane

M. Nakazaki, M. Hashimoto, K. Naemura, 1983 .

SYNTHESES AND CHIROPTICAL PROPERTIES OF OPTICALLY ACTIVE C1-METHANOTWISTANE, C2-DITWISTANE, C1-HOMOBASKETANE, AND C2-3,10-DEHYDRODITWISTANE

M. Nakazaki, M. Hashimoto, K. Naemura, 1980 .

Syntheses of novel gyrochiral pentacyclic systems with C2 symmetry. (-)-C2-Bismethanotwistane and (.+-.)-C2-methanoditwistane

M. Nakazaki, K. Naemura, Masamichi Iwasaki, 1979 .

Synthesis of (+)-1,3,5,7 -tetrakis[2-(1S,3S,5R,6S,8R,10R)-D3-trishomocubanylbuta-1,3-diynyl]adamantane

M. Nakazaki, K. Naemura, Yukio Hokura, 1986 .

Synthesis of (+)-1,3,5,7 -tetrakis[2-(1S,3S,5R,6S,8R,10R)-D3-trishomocubanylbuta-1,3-diynyl]adamantane : The first optically active organic molecule with t symmetry and of known absolute configuration

M. Nakazaki, K. Naemura, Yukio Hokura, 1986 .

Total Synthesis of (−)-Artemisin

M. Nakazaki, K. Naemura, 1969 .

A new entry to [6](1,4)naphthalenophane and [6](1,4)anthracenophane: Synthesis of peri-substituted derivatives

Y. Tobe, K. Naemura, Shinji Saiki, 1995 .

Absolute Configurations and Chiroptical Properties of Optically Active Derivatives of Tricyclo[4.3.0.03,8]nonane (“Twist-brendane”)

M. Nakazaki, K. Naemura, S. Harita, 1975 .

Photolyses of Isobornyl and Bornyl Nitrites

M. Nakazaki, K. Naemura, 1964 .

Homochiral ligands derived from cis-1-phenylcyclohexane-1,2-diol and cis-2-azido-2-phenylcyclohexanol

Y. Tsuchiya, Y. Tobe, M. Konishi, 1997 .

Synthesis and Enantiomer Recognition of Dipodands and Crown Ethers Containing the 2,3:6,7-Dibenzobicyclo[3.3.1]nona-2,6-diene Residue as the Chiral Subunit

M. Komatsu, K. Naemura, H. Chikamatsu, 1989 .

Synthesis and enantiomer recognition of novel crown ethers containing the 5,6,11,12-tetrahydro-5,11-methanodibenzo[a,e]cyclo-octene subunit as the chiral centre

K. Naemura, M. Yamanaka, R. Fukunaga, 1985 .

Stereoselective conversion of keto groups into methyl vinyl quaternary carbon centers

P. Wovkulich, H. Felkin, E. Wenkert, 1978 .

Preparation and enantiomer recognition of chiral azophenolic crown ethers having three chiral barriers on each of the homotopic faces

Masaki Asada, Keiji Hirose, Keiji Hirose, 1995 .

Asymmetric hydride reduction using a chiral aluminium reagent modified by a crowned 2,2′-dihydroxy-1,1′-binaphthyl

Koji Yamamoto, K. Ueno, K. Naemura, 1991 .

Preparation of optically active azophenolic crown ethers containing 1-phenylethane-1,2-diol and 2,4-dimethyl-3-oxapentane-1,5-diol as a chiral subunit: temperature-dependent enantiomer selectivity in the complexation with chiral amines1

Keiji Hirose, Y. Tobe, K. Naemura, 1997 .

Preparation of chiral and meso-crown ethers incorporating cyclohexane-1,2-diol derivatives as a steric barrier and their complexation with chiral and achiral amines

Y. Tobe, K. Naemura, T. Kaneda, 1996 .

Preparation of homochiral phenolic crown ethers containing para-substituted phenol moiety and chiral subunits derived from (S)-1-phenylethane-1,2-diol: their chiral recognition behaviour in complexation with neutral amines

Keiji Hirose, Y. Tobe, Junichi Fuji, 1997 .

Supramolecular method for the determination of absolute configuration of chiral compounds: theoretical derivatization and a demonstration for a phenolic crown ether-2-amino-1-ethanol system.

Keiji Hirose, Keiji Hirose, Y. Tobe, 2007, Analytical chemistry.

Synthesis of Chiral Crown Ethers Derived from trans, trans- and cis, trans-2,2′-Spirobiindan-1,1′-diols. Their Chiral Recognition and Complexation Properties

M. Nakazaki, K. Naemura, I. Ebashi, 1985 .

Remarkable Effect of Subtle Structural Change of Chiral Pseudo-18-Crown-6 on Enantiomer-Selectivity in Complexation with Chiral Amino Alcohols

Keiji Hirose, Y. Tobe, Michiko Suzuki, 2005 .

Preparation and temperature-dependent enantioselectivities of homochiral phenolic crown ethers having aryl chiral barriers: thermodynamic parameters for enantioselective complexation with chiral amines

Keiji Hirose, Y. Tobe, K. Naemura, 1998 .

Preparation of a Homochiral Phenolic Crown Ether Having Chiral Subunits Derived from (1R,2S)-cis-1,2,3,4-Tetrahydronaphthalene-1,2- diol: Temperature-Dependent Enantioselectivity in Complexations with Neutral Amines.

Keiji Hirose, Y. Tobe, K. Naemura, 1997 .

Preparation and enantiomer recognition behaviour of azophenolic crown ethers containing cis-1-phenylcyclohexane-l,2-diol as the chiral subunit and 2,4-dinitrophenylazophenol as the chromophore

Keiji Hirose, Y. Tobe, Y. Sakata, 1996 .

Temperature dependent reversal of enantiomer selectivity in the complexation of optically active phenolic crown ethers with chiral amines

Keiji Hirose, Y. Tobe, Junichi Fuji, 1996 .

Preparation and enantiomer recognition behaviour of azophenolic crown ethers containing cis-cyclohexane-1,2-diol as the chiral centre

Takahiro Kaneda, Yoshiteru Sakata, Keiji Hirose, 1995 .

Synthesis of azophenolic crown ethers of Cs symmetry incorporating cis-1-phenylcyclohexane-1,2-diol residues as a steric barrier and diastereotopic face selectivity in complexation of amines by their diastereotopic faces

Masaki Asada, Takahiro Kaneda, Yoshiteru Sakata, 1995 .

The synthesis of azophenolic crown ethers of Cs symmetry incorporating cis-1-phenylcyclohexane-1,2-diol residues and diastereotopic face selectivity in complexation of ethanolamine by their diastereotopic faces

Keiji Hirose, Y. Tobe, Y. Sakata, 1994 .

Preparation of Optically Active Azophenolic Crown Ethers Containing 1-Phenylethane-1,2-diol and 2,4-Dimethyl-3-oxapentane-1,5-diol as a Chiral Subunit (I)—(IV): Temperature-Dependent Enantiomer Selectivity in the Complexation with Chiral Amines.

Keiji Hirose, Y. Tobe, K. Naemura, 1998 .

Azophenolic acerands having chiral 1-phenyl-cis-1,2-cyclohexanediol units : a correlation between enantiorecognitive coloration and host-guest complementarity

Y. Tobe, Y. Sakata, K. Ueno, 1993 .

16.16.16(1,3,5)CYCLOPHANETETRACOSAYNE (C60H6) : A PRECURSOR TO C60 FULLERENE

Y. Achiba, Y. Tobe, Tomonari Wakabayashi, 1998 .

Synthesis and Characterization of [6](9,10)Anthracenophane

Y. Tobe, N. Utsumi, K. Naemura, 1994 .

The Synthesis and Absolute Configuration of Optically Active Tricyclo[4.3.0.03,8]nonane (Twist-brendane)

M. Nakazaki, K. Naemura, 1973 .

Synthesis and lithium ion selectivity of 14-crown-4 derivatives having bulky subunits: cis and trans isomers of 2-phenylcyclohexano-14-crown-4, 2,3-diphenylcyclohexano-14-crown-4 and 2,3-di-(1-adamantyl)-14-crown-4

Y. Tsuchiya, Koji Suzuki, Y. Tobe, 1998 .

Synthesis and Lithium Ion-Selectivity of 2-Phenylcyclohexano- and 2,3-Diphenylcyclohexano-14-crown-4 Derivatives

Y. Tobe, K. Suzuki, K. Kobiro, 1995 .

Synthesis of Novel Bis-Crown and Double-Armed Crown Ethers Having the 18-Crown-6 Residue

K. Naemura, H. Chikamatsu, Hiroshi Iwasaka, 1987 .

Synthesis of chiral 18-crown-6 derivatives and dibenzocrown ethers incorporating trans-tetrahydrofuran-2,5-diylbis(methylene) units of known absolute configuration

A. Matsuda, K. Naemura, I. Ebashi, 1985 .

Optically active cumulene synthesis and resolution of 1,5-di-- chlorophenyl-1,5-di-t-butyl-pentatetraene

K. Shingū, K. Naemura, M. Nakagawa, 1961 .

Lipase YS-Catalyzed Enantioselective Transesterification of Alcohols of Bicarbocyclic Compounds

K. Naemura, Ritsuko Fukuda, Hirotsugu Ida, 1993 .

Synthesis and Enantiomer Recognition of the 18-Crown-6 Derivative Containing Two Tert-Butyl Substituents as a Chiral Barrier

M. Ueno, K. Naemura, 1990 .

Preparation of Chiral and meso‐Crown Ethers Incorporating Cyclohexane‐ 1,2‐diol Derivatives as a Steric Barrier and Their Complexation with Chiral and Achiral Amines

Y. Tobe, K. Naemura, T. Kaneda, 1996 .

Synthesis and enantiomer recognition of crown ethers containing cyclohexane-1,2-diol derivatives as the chiral centre and enzymatic resolution of the chiral subunits

Yasuhiro Shingai, K. Naemura, H. Miyabe, 1991 .

Enzymatic Hydrolysis of 2,6-Diacetoxybicyclo(3.3.1)nonane and 2,6-Diacetoxy-3,3,7,7-tetramethylbicyclo(3.3.1)nonane. A Facile Synthesis of the Optically Active Chiral Subunit for Crown Ethers.

M. Komatsu, K. Naemura, H. Chikamatsu, 1988 .

Enzymatic hydrolysis of 2,6-diacetoxybicyclo[3.3.1]nonane and 2,6-diacetoxy-3,3,7,7-tetramethylbicyclo[3.3.1]nonane; a facile synthesis of the optically active chiral subunit for crown ethers

M. Komatsu, K. Naemura, H. Chikamatsu, 1988 .

Enantiomer recognition of crown ethers and open-chain polyethers containing the trans-tetrahydrofuran-2,5-diylbis(methylene) subunit as the chiral centre

A. Matsuda, K. Naemura, H. Chikamatsu, 1986 .

Preparation of Homochiral Phenolic Crown Ethers Containing para- Substituted Phenol Moiety and Chiral Subunits Derived from (S)-1- Phenylethane-1,2-diol: Their Chiral Recognition Behavior in Complexation with Neutral Amines.

Keiji Hirose, Y. Tobe, Junichi Fuji, 1997 .

Syntheses of Tetracyclo[7.3.0.03,7.04,10]dodecane-2,8-dione (“[8]Diisotwistane-2,8-dione”) and8,9-Benzotricyclo[4.3.1.03,7]decane (“Benzoisotwistane”)

M. Nakazaki, K. Naemura, H. Yoshihara, 1975 .

Horse liver alcohol dehydrogenase-catalyzed enantioselective reduction of cyclic ketones: The effect of the hydrophobic side chain of the substrate on the stereoselectivity of the reaction

Toshihiko Matsumoto, Y. Hirose, K. Naemura, 1995 .

SELECTIVE AND STEREOSPECIFIC HORSE LIVER ALCOHOL DEHYDROGENASE-CATALYZED REDUCTION OF CAGE-SHAPED meso-DIKETONE. AN EFFICENT ACCESS TO OPTICALLY ACTIVE D3-TRISHOMOCUBANE DERIVATIVE

K. Naemura, Takanori Fujii, H. Chikamatsu, 1986 .

Selective and Stereospecific Horse Liver Alcohol Dehydrogenase-Catalyzed Reduction of Cage-Shaped meso-Diketone.

K. Naemura, H. Chikamatsu, T. Fujii, 1986 .

Syntheses and chiroptical properties of (-)-ditwist-brendane and (+)-D3-trishomocubane

M. Nakazaki, K. Naemura, Nobumasa Arashiba, 1978 .

Horse Liver Alcohol Dehydrogenase‐Catalyzed Enantioselective Reduction of Cyclic Ketones: The Effect of the Hydrophobic Side Chain of the Substrate on the Stereoselectivity of the Reaction.

Toshihiko Matsumoto, Y. Hirose, K. Naemura, 1996 .

Synthesis and Facile Rearrangement of 10, 10-Dicarbonyl-substituted [4. 3. 1]Propellane Derivatives

Y. Tobe, M. Sonoda, R. Umeda, 2003 .

Synthesis and absolute configuration of the first optically active organic molecule with T symmetry: (-)-1,3,5,7-tetrakis[[(2-(1S,3S,5R,6S,8R,10R)-D3-trishomocubanyl)acetoxy]methyl]adamantane

M. Nakazaki, K. Naemura, 1981 .

SYNTHESES AND CHIROPTICAL PROPERTIES OF (+)‐2‐BRENDANONE AND ITS ANALOGS

M. Nakazaki, K. Naemura, Y. Kondo, 1979 .

Absolute configurations and absolute rotations of C2-bishomocubane, ditwist-brendane, and twistane

M. Nakazaki, K. Naemura, S. Nakahara, 1978 .

SYNTHESES AND CHIROPTICAL PROPERTIES OF (‐)‐DITWIST‐BRENDANE AND (+)‐D3‐TRISHOMOCUBANE

M. Nakazaki, K. Naemura, Nobumasa Arashiba, 1978 .

Synthesis and absolute configuration of (-)-D2d-bisnoradamantan-2-one (tricyclo[3.3.0.03,7]octan-2-one)

M. Nakazaki, K. Naemura, Nobumasa Arashiba, 1978 .

SYNTHESIS AND ABSOLUTE CONFIGURATION OF OPTICALLY ACTIVE C2‐BISHOMOCUBANE (PENTACYCLO(5.3.0.02,5.03,9.04,8)DECANE)

M. Nakazaki, K. Naemura, 1978 .

Syntheses and absolute configurations of tricyclo[4.3.0.03,7]nonane ("brexane"), 3-oxatricyclo[4.3.0.04,9]nonane ("3-oxabrexane"), and tricyclo[4.2.0.03,7]octan-2-one ("norbrexan-2-one")

M. Nakazaki, K. Naemura, H. Kadowaki, 1976 .

Syntheses and chiroptical properties of optically active derivatives of tricyclo[3.3.0.03,7]octane and oxatricyclononanes

M. Nakazaki, K. Naemura, Y. Kondo, 1976 .

Polyyne cyclization to form carbon cages: [16.16.16](1,3,5)cyclophanetetracosayne derivatives C60H6 and C60Cl6 as precursors to C60 fullerene

Y. Achiba, Y. Tobe, M. Sonoda, 2001 .

Lipase-catalysed asymmetric and enantioselective esterification of spiro[3.3]heptanes in organic solvents

K. Naemura, A. Furutani, 1991 .

Diels-Alder Reactions of Tetraethynylcyclopentadienones. An Approach to Differentially Substituted Hexaethynylbenzenes of C2v Symmetry.

Y. Tobe, K. Naemura, K. Kubota, 1997 .

Synthesis and absolute configuration of optically active C2-bishomocubane (pentacyclo[5.3.0.02,5.03,9.04,8]decane)

M. Nakazaki, K. Naemura, 1977 .

The Synthesis of Organic Molecules with Polyhedral Symmetry

K. Naemura, 1987 .

Syntheses and Stereochemistry of High Symmetry Cage-Shaped Compounds

M. Nakazaki, K. Naemura, 1977 .

The Biogenetic-Type Cyclization of the Unsaturated Monocyclic Alcohol with Formic Acid; Facile Synthesis of the Tricarbocyclic Alcohol, (+)-2-Epi-allo-cedrol

T. Hasegawa, K. Naemura, H. Chikamatsu, 1992 .

Photoelectron spectroscopy of C-n produced from laser ablated dehydroannulene derivatives having carbon ring size of n=12, 16, 18, 20, and 24

Y. Achiba, T. Momose, M. Kohno, 1997 .

The Conversion of (-)-a-Santonin into (-)--Santonin

M. Nakazaki, K. Naemura, 1964 .

Synthesis and Anion Binding Ability of Metacyclophane-Based Cyclic Thioureas

S. Sasaki, Y. Tobe, K. Naemura, 1998 .

Synthesis and Anion Binding Ability of Metacyclophane-Based Cyclic Thioureas.

S. Sasaki, Y. Tobe, K. Naemura, 1998 .

Preparation of homochiral crown ether containing (S)-1-(1-adamantyl)ethane-1,2-diol as a chiral subunit and its enantioselective complexation with an organic ammonium cation

K. Kamada, Keiji Hirose, Y. Tobe, 1994 .

SYNTHESIS AND ABSOLUTE CONFIGURATION OF (−)-D3-TRITWISTANE, (−)-(1S,3S,6S,7S,10S,12S)PENTACYCLO[8.4.0.02,7.03,12.06,11]TETRADECANE

M. Nakazaki, M. Hashimoto, K. Naemura, 1980 .

Synthesis of (+)-1,3,5,7-tetrakis[2-(1S,3S,5R,6S,8R,10R)-D3-trishomocubanylbuta-1,3-diynyl] adamantane. An optically active organic molecule with T symmetry and of known absolute configuration

M. Nakazaki, K. Naemura, Yukio Hokura, 1982 .

Circular‐dichroism power of chiral, bridged, aromatic compounds. 7,8,15,16‐Tetrahydro‐7,15‐methanocycloocta[1,2‐a:5,6‐a′]dinaphthalene derivatives

N. Harada, K. Naemura, Norie Hiyoshi, 2010 .

Enantioselective Acylation of Alcohols Catalyzed by Lipase QL from Alcaligenes sp.: A Predictive Active Site Model for Lipase QL to Identify the Faster Reacting Enantiomer of an Alcohol in this Acylation.

Keiji Hirose, Y. Tobe, K. Naemura, 1996 .

Synthesis of the Himachalenes by an Intramolecular Diels-Alder Reaction Route

E. Wenkert, K. Naemura, 1973 .

Preparation of homochiral azophenolic crown ethers containing 1-phenylethane-1,2-diol and 2,4-dimethyl-3-oxapentane-1,5-diol as a chiral subunit: Enantiomer recognition behaviour towards chiral 2-aminoethanol derivatives

Keiji Hirose, Y. Tobe, K. Naemura, 1997 .