T. Moriwake

发表

Hydrogen azide-amine systems as an azide nucleophile for substitutions of sulfonates, halides, and vicinal disulfonates

S. Saitô, H. Yokoyama, T. Ishikawa, 1991 .

A revised mechanism for chemoselective reduction of esters with borane-dimethyl sulfide complex and catalytic sodium tetrahydroborate directed by adjacent hydroxyl group

Kazuya Koga, S. Saitô, T. Ishikawa, 1992 .

Combination of borane-dimethyl sulfide complex with catalytic sodium tetrahydroborate as a selective reducing agent for α-hydroxy esters, versatile chiral building block from (S)-(-)-malic acid

M. Inaba, T. Hasegawa, S. Saitô, 1984 .

Solvolysis in Carboxamides. II. Solvolytic Elimination of 7β-Methylbicyclo[3.3.1]non-3β-yl Tosylate in Carboxamides

S. Saitô, T. Moriwake, K. Okamoto, 1978 .

Solvolysis of cis- and trans-4-t-Butylcyclohexyl Tosylates in N-Methylacetamide. Rates and Products Distribution

S. Saitô, T. Moriwake, K. Okamoto, 1973 .

A SELECTIVE 1,2-REDUCTION OF γ-AMINO-α,β-UNSATURATED ESTERS BY MEANS OF BF3·OEt2-DIBAL-H SYSTEM. HIGHLY VERSATILE CHIRAL BUILDING BLOCKS FROM α-AMINO ACIDS

S. Saitô, T. Moriwake, S. Hamano, 1986 .

One-pot transformation of azido-group to N-(t-butoxycarbonyl)amino group

M. Inaba, H. Nakajima, S. Saitô, 1989 .

Efficient nucleophilic oxirane ring cleavage with dibutyltin diazide

S. Saitô, T. Moriwake, Toshiya Nishikawa, 1990 .

Highly nucleophilic tributyltin azide in oxirane ring cleavage leading to 1,2-azido alcohol

M. Inaba, S. Saitô, T. Moriwake, 1989 .

High differentiation of the diastereo .pi.(C:C)-faces of acyclic bis-allylic systems in osmium tetroxide-catalyzed dihydroxylation

S. Saitô, T. Moriwake, Y. Morikawa, 1990 .

A New Synthesis of (—)-Isopretronecanol and (—)-Trachelanthamidine through Orthoester Claisen Rearrangement for Allylic Alcohol Functionality Tagged at C(2) of Pyrrolidine as a Key Step

S. Saitô, T. Moriwake, S. Hamano, 1988 .

Rotamer distribution control and double Michael addition for cyclopentane annulation with superb selectivity

Y. Hirohara, S. Saitô, T. Moriwake, 1989 .

Chiral Template Approach to 1,2-Disubstituted Carbacephem Antibiotics: Highly Chemoselective Reactions of Bicyclic Lactam Intermediates Bearing Multi-Carbonyl Functions with Nucleophiles

S. Saitô, T. Ishikawa, T. Moriwake, 1993 .

Diethyl (2S,3R)‐2‐(N‐tert‐butoxycarbonyl)amino‐ 3‐Hydroxysuccinate

S. Saitô, T. Moriwake, K. Komada, 2003 .

A Straightforward Synthesis of Allyl Amines from α-Amino Acids without Racemization

S. Saitô, T. Moriwake, S. Hamano, 1987 .

Activation of manganese metal by a catalytic amount of PbCl2 and Me3SiCl

K. Takai, T. Moriwake, T. Ueda, 1996 .

Synthesis of axially dissymmetric 3,5-octadiene framework with C2 chirality via palladium(II)-catalyzed twofold [3,3]sigmatropic rearrangement

K. Okada, S. Saitô, T. Moriwake, 1988 .

A new, highly efficient method for isocarbacyclin synthesis based on tandem Claisen rearrangement and ene reactions

J. Tsuji, S. Saitô, T. Moriwake, 1990 .

Sequential Generation and Utilization of Radical and Anionic Species with a Novel Manganese-Lead Reducing Agent. Three-Component Coupling Reactions of Alkyl Iodides, Electron-Deficient Olefins, and Carbonyl Compounds.

K. Takai, T. Moriwake, T. Ueda, 1996, The Journal of organic chemistry.

Transformation of Aldehydes into (E)-1-Alkenylboronic Esters with a Geminal Dichromium Reagent Derived from a Dichloromethylboronic Ester and CrCl2

K. Takai, T. Moriwake, K. Utimoto, 1995 .

EFFICIENT SYNTHESIS OF SECONDARY CARBOXAMIDES WITH ω-SUBSTITUTED ETHYL AND PROPYL GROUPS ON NITROGEN ATOM BY NUCLEOPHILIC RING OPENING OF CYCLIC IMIDATES

M. Inaba, Y. Usui, S. Saitô, 1984 .

Sequential 1,4-Addition and Ireland-Claisen Rearrangement Promoted by a Manganese-PbCl(2)-Me(3)SiCl System(1).

K. Takai, T. Moriwake, T. Ueda, 1996, The Journal of organic chemistry.

Selective C-2 opening of 2,3-epoxyesters with HN3-amine system: A viable route to β-hydroxy-α-amino acids

S. Saitô, T. Ishikawa, T. Moriwake, 1991 .

Novel approach to stereoisomerically full set of optically pure 2,3-epoxyesters from tartaric acids

M. Inaba, Y. Nagao, S. Saitô, 1986 .

One-Pot Transformation of Azido-Group to N-(tert-Butoxycarbonyl)amino Group.

M. Inaba, H. Nakajima, S. Saitô, 1989 .

Selective One-Pot Synthesis of Allenyl Phenyl Selenide and 1-(Phenylseleno)Propyne. Role of Sodium Benzeneselenolate as a Base in Dmf

M. Inaba, S. Saitô, T. Moriwake, 1984 .

Tandem reductive amination and Michael addition. Synthesis of optically active pyrrolidine nucleus

S. Matsumoto, M. Inaba, S. Saitô, 1986 .

Tandem Reductive Amination and Michael Addition. Synthesis of Optically Active Pyrrolidine Nucleus.

S. Matsumoto, M. Inaba, S. Saitô, 1987 .

Tandem Dianionic Dioxy-Cope Rearrangement and Aldol Condensation: A Single-Pot Enantioselective Route to trans-4,5-Disubstituted 1-Cyclopentenecarbaldehyde from Acyclic Bisallylic Compounds

S. Saitô, T. Moriwake, M. Matsuoka, 1992 .

Conformational diagnosis of diethyl (4S,5S)-4,5-bis(tert-butyldimethylsiloxy)-2E,6E-octadienedioate based on the stereochemical outcomes of representative reactions as compared with those of its 4,5-O-isopropylidene derivatives and on a dichroic exciton chirality method

J. Gawroński, S. Saitô, T. Ishikawa, 1993 .

Vicinal diol controller approach to highly diastereoselective hydroxy-directed MCPBA epoxidations of allylic alcohols with oxygen-bearing stereocenters

H. Itoh, S. Saitô, T. Moriwake, 1993 .

A facile cleavage of oxirane with hydrazoic acid in DMF a new route to chiral β-hydroxy-α-amino acids

M. Inaba, S. Saitô, T. Moriwake, 1985 .

Vicinal Diol Controller Approach to Highly Diastereoselective Hydroxy‐ Directed MCPBA Epoxidations of Allylic Alcohols with Oxygen‐Bearing Stereocenters.

H. Itoh, S. Saitô, T. Moriwake, 1993 .

Protected vicinal diol controller in diastereoselective reduction of β-oxo esters

S. Saitô, T. Moriwake, M. Asahara, 1992 .

Enantioselective Synthesis of Functionalized Cyclopentenone and Alkylidenecyclopentane Derivatives from an Acyclic Bisallylic Diol Framework

K. Naka, S. Saitô, T. Moriwake, 1992 .

A Chiral Acyclic Bis-allylic Compound as a Dienophile for Asymmetric Diels-Alder Reactions

H. Hama, K. Okada, S. Saitô, 1991 .

Synthesis of Optically Pure 2,3,4,5-Substituted Tetrahydrofurans from a Bis-Allylic Framework via an Osmylation-Haloetherification Sequence

S. Saitô, T. Moriwake, Y. Morikawa, 1990 .

Solvolysis in Carboxamides. IV. Solvolytic Elimination of exo-2-Norbornyl Arenesulfonates in Carboxamides. Kinetic, Product, and Deuterium Tracer Studies

K. Takeuchi, S. Saitô, T. Moriwake, 1978 .

Synthesis of the chiral (8S)-7-aza-1,3(E),9-decatriene system from natural .alpha.-amino acids and its intramolecular Diels-Alder reaction directed toward chiral trans-hydroisoquinolones

S. Kashino, S. Saitô, T. Moriwake, 1989 .

Solvolysis in carboxamides. VII. Carboxamide solvolysis of threo-2-aryl-1-methylpropyl brosylates. Reactivity-selectivity relationships as a mechanistic probe.

S. Saitô, T. Moriwake, K. Okamoto, 1979 .

Solvolysis in Carboxamides. V. Solvolytic Elimination of threo-1-Methyl-2-phenylpropyl Brosylate in N,N-Dimethylacetamide. Kinetic, Product, and Deuterium Tracer Studies

S. Saitô, T. Moriwake, K. Okamoto, 1979 .

Solvolysis in Carboxamides. III. Solvolysis Rates of 1-Adamantyl Bromide and Tosylate, 2-Adamantyl Tosylate, and t-Butyl Chloride in Carboxamides

S. Saitô, T. Moriwake, K. Okamoto, 1978 .