PB102 SYNTHESES OF THE OPTICALLY ACTIVE FORMS OF THE MUS MUSCULUS PHEROMONE
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概要
- 論文の詳細を見る
- 天然有機化合物討論会の論文
- 1988-05-29
著者
-
MASAKI Yukio
Gifu Pharmaceutical University
-
Oda Hirohisa
Gifu Pharmaceutical University
-
IMAEDA Toshihiro
Gifu Pharmaceutical University
-
Nagashima Hiromu
Gifu College of Pharmacy
-
Iwata Ikuhiro
Gifu Pharmaceutical University
関連論文
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- Oxidative Photo-Decarboxylation in the Presence of Mesoporous Silicas
- New Synthetic Method of Imides through Oxidative Photodecarboxylation Reaction of N-Protected α-Amino Acids with FSM-16
- Synthesis of (R)-(+)-Tanikolide through Stereospecific C-H Insertion Reaction of Dichlorocarbene with Optically Active Secondary Alcohol Derivatives
- Stereospecific Construction of Chiral Quaternary Carbon Compounds from Chiral Secondary Alcohol Derivatives
- Polymer-Supported Dicyanoketene Acetal as a π-Acid Catalyst : Monothioacetalization and Carbon-Carbon Bond Formation of Acetals
- Mild Esterification and Transesterification of Carboxylic Acids Catalyzed by Tetracyanoethylene and Dicyanoketene Dimetheyl Acetal
- SYNTHESIS OF (+)-7-ETHYL-5-METHYL-6,8-DIOXABICYCLO[3,2,1]OCT-3-ENE, An OPTICALLY ACTIVE FORM OF THE HOUSE MOUSE PHEROMONE
- Pyridazino〔4,5-e〕-1,2,4-triazineの誘導体の合成と除草作用
- Studies on Syntheses and Reactions of Methoxypyridazines. II. Methoxylation of 3,4,6-Trichloropyridazine(Organic,Chemical)
- 26 酒石酸を不斉源とする(+)-アスペルリンの全合成(口頭発表の部)
- Asymmetric Synthesis of (+)-Dihydrokawain-5-ol.
- Facile Synthesis of Optically Active Tertiary Alcohol Building Blocks by Stereospecific C - H Insertion Reaction of Dichlorocarbene with Secondary Alcohol Derivatives
- A highly asymmetric, Lewis Acid-catalysed Diels-Alder reaction using optically active 2-(3-tolyl-p-sulfinyl)furyl α, β-unsaturated ketones as a dienophile.
- Stereoselective Reduction of Chiral 3-(p-Tolylsulfinyl)-2-thienyl Ketones. : A Facile Entry to Optically Active Thienylcarbinols.
- Highly Stereoselective Hetero Diels-Alder Reactions of Chiral 3-(p-Tolylsulfinyl)-2-furaldehyde with Danishefsky's Diene Promoted by a Lanthanoid Lewis Acid.
- Stereoselective Reduction of Chiral 3-(p-Tolylsulfinyl)-2-thienyl Ketones. A Facile Entry to Optically Active Thienylcarbinols
- Total Synthesis of (+)-Asperlin Starting with (S,S)-Tartaric Acid
- Deprotection of a Silyl Group with Mesoporous Silica
- New Synthetic Method of Benzaldehydes and α,β-Unsaturated Aldehydes with I_2 under Photoirradiation
- The Synthesis of Sulfur-Containing Pyridazines. I. Benzylthiolation with a Subsequent Selective Debenzylation on 4,5-Dihalo-3-Pyridazones.
- Diastereoselective Imino-Aldol Condensation of Chiral 3-(p-Tolylsulfinyl)-2-furaldimine and Ester Enolates
- β-Lactam Synthesis by Diastereoselective Condensation of Chiral 3-(p-Tolylsulfinyl)-2-Furaldimine and Ester Enolates.
- Recoverable Chiral Sulfoxide : Remote Asymmetric Induction in Lewis Acid-Promoted Diels-Alder Reaction of Chiral Sulfinyl-Substituted Pyrrolylα, β-Unsaturated Enones.
- Remote Asymmetric Induction in Lewis Acid Catalyzed Diels-Alder Reaction of α, β-Unsaturated Enones Having a Chiral Sulfinyl-substituted, 5-Membered Aromatic Heterocycle.
- Remote Asymmetric Induction in Lewis Acid-Catalyzed Diels-Alder Reaction of α, β-Unsaturated Enones Having a Chiral Sulfinyl-Substituted, 5-Membered Aromatic Heterocycle
- Highly Stereoselective Aldol Reaction of Chiral 3-(p-Tolylsulfinyl)furfural with Silyl Ketene Acetal Catalyzed by Lanthanide Triflate
- Recoverable Chiral Sulfoxide : Asymmetric Diels-Alder Reaction Using Optically Active 1-(2-p-Tolylsulfinyl)pyrrolyl α, β-Unsaturated Ketones as a Dienophile
- Diastereoselective Addition of Allyltriphenylstannane to 3-Sulfinylfurfural Mediated by Titanium (IV) Tetrachloride and Tin(IV) Tetrachloride.
- Alocoholysis of Epoxides Catalyzed by Tetracyanoethylene and Dicyanoketene Acetals
- Substrate-Specific Rearrangement and Acetonidation of Epoxy-Ethers Catalyzed by Tetracyanoethylene
- Synthesis of (Z)-1,2-Dihalo-1-alkenes by the Reaction of (Z)-(β-Halovinyl)phenyliodonium Salts with n-Bu4NX or KX/CuX. Competitions between Nucleophilic Vinylic Substitutions and Aromatic Substitutions
- Synthesis of Chiral Sulfinyl-Substituted 1-Indolyl Enones and Asymmetric Conjugate Addition by an Arylcopper Reagent
- PB102 SYNTHESES OF THE OPTICALLY ACTIVE FORMS OF THE MUS MUSCULUS PHEROMONE
- Recyclable Polymeric π-Acid Catalyst Effective on Mannich-Type Reaction in Water
- Synthesis of (3S,4S)-Statine and a Related Compound, (3S,4S)-AHPPA, from _D-Glucosamine as a Chiral Pool
- Enantiospecific Synthesis of (3S, 4S)-Statine and Its Analogue from D-Glucosamine as a Chiral Pool
- Chiral Syntheses of Dihydroxyamino Acid Moieties of AI-77-B and Calyculins from D-Glucosamine
- Synthesis of D-erythro-Sphingosine from D-Glucosamine
- Recoverable Chiral Sulfoxide : Asymmetric Diels-Alder Reaction Usig Optically Active 1-(2-p-Tolylsulfinyl) pyrrolyl α, β-Unsaturated Ketones as a Dienophile
- C_2-SYMMETRIC N-(β-MERCAPTOETHYL)PYRROLIDINE AS A CHIRAL CATALYST LIGAND IN THE ADDITION REACTION OF ALDEHYDES AND DIETHYLZINC
- 1, 6-Asymmetric Induction during the Conjugate Addition of Arylcopper Reagents to a Chiral Sulfinyl-Substituted Pyrrolyl α, β-Unsaturated Amide