Double Stereocontrol in α-Alkylation of Chiral Lithium Dienolates Generated from (E)-α,β-Olefinic Amides and Esters
スポンサーリンク
概要
- 論文の詳細を見る
- 1998-10-05
著者
-
Tomooka K
Department Of Chemical Technology Tokyo Institute Of Technology
-
Tomooka Katsuhiko
Department Of Chemistry Keio University
-
Tomooka K
Tokyo Inst. Technol. Tokyo
-
Tomooka Katsuhiko
Department Of Applied Chemistry Tokyo Institute Of Technology
-
NAKAI Takeshi
Department of Chemical Technology, Tokyo Institute of Technology
-
Nagasawa Atsushi
Department of Cardiovascular Surgery, Graduate School of Medicine
-
Nakai Takeshi
Department Of Applied Chemistry Tokyo Institute Of Technology
-
Nagasawa Atsushi
Department Of Cardiovascular Surgery Graduate School Of Medicine
-
Nagasawa Atsushi
Department Of Chemical Technology Tokyo Institute Of Technology
関連論文
- Stereochemistry and Mechanism of Vinyl-migrating [1, 2]-Wittig Rearrangement of α-Lithioalkyl Vinyl Ethers
- 1, 2-Carbamoyl Migration on Enantio-enriched α-Lithioalkyl Carbamates Generated with s-Butyllithium/Sparteine:Steric Course and Mechanism
- Ortho-[2,3]-Wittig Rearrangement of Benzyl Propargyl Ethers: Striking Preference over the Competing [1,2]-Wittig Shift
- Sustained-Release Erythropoietin Ameliorates Cardiac Function in Infarcted Rat-Heart Without Inducing Polycythemia
- 3 Efficient and Specific Expansion of Highly Cardiogenic Progenitors from Embryonic Stem Cells by Cyclosporin-A Treatment(Young Investigator's Award for International Students Finalists Lecture (YIA International),Special Program,The 72nd Annual Scientifi
- P-406 Enantioselective Hydroalumination of Prochiral Propargylic Alcohol : An Efficient Stereoselective Approach to Functionalized Chiral tert-Alcohol
- Double Stereocontrol in α-Alkylation of Chiral Lithium Dienolates Generated from (E)-α,β-Olefinic Amides and Esters
- PB163 Stereocontrolled Total Synthesis of Mycinamicin IV
- Enrichment of Ce@C_ by HPLC Technique
- Stereocontrol by Lewis Acids in the Hetero-Diels-Alder Reaction Leading to a Key 1β-Methylcarbapenem Intermediate
- [2, 3]-Witting Rearrangement of Crotyl Picolyl Ethers. Evaluation of the Electronic Effect as a Stereo-Directing Factor
- Conversion of Tar in Hot Coke Oven Gas by Pyrolysis and Steam Reforming
- PB108 INTRAMOLECULAR ENE APPROACHES TO STEREOCONTROL OVER CONTIGUOUS CHIRAL CENTERS
- [1, 2] -Wittig Rearrangement Stereochemical Features and Synthetic Utilities
- Unique Stereocontrol in Europium (III)-Catalyzed Cyanosilylation of Chiral α-Alkoxy and α-Amino Aldehydes
- Stereo-Mudulating Catalysis by Enropium(III) Complexes in Aldol Reactions of Chiral α-Alkoxy Aldehydes with Ketene Silyl Acetals
- Plastic Surgical Reconstruction of Left Main Coronary Artery
- Stereochemical Feature of Palladium(II)-Catalyzed Claisen Rearrangement
- [1,2]-Wittig Rearrangement : Stereochemical Features and Synthetic Utilities
- A convenient preparation of arylthioynamines.
- Competitive cyclization in the reaction of hexafluoropropene with 2-aminobenzamide.
- Synthetic studies of erythromycins. IV. Total synthesis of erythronolide A.