Iwasawa et al., 1989 - Google Patents
Characterization of the chiral titanium reagent prepared from the tartrate-derived chiral diol and titanium dichloride diisopropoxide.Iwasawa et al., 1989
- Document ID
- 8300467533860550958
- Author
- Iwasawa N
- Hayashi Y
- Sakurai H
- Narasaka K
- Publication year
- Publication venue
- Chemistry Letters
External Links
Snippet
Hidehiro SAKURAI, and Koichi NARASAKA Page 1 CHEMISTRY LETTERS, pp. 1581-1584,
1989. © 1989 The Chemical Society of Japan Characterization of the Chiral Titanium Reagent
Prepared from the Tartrate-derived Chiral Diol and Titanium Dichloride Diisopropoxide …
- 239000003153 chemical reaction reagent 0 title abstract description 22
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Iwasawa et al. | Characterization of the chiral titanium reagent prepared from the tartrate-derived chiral diol and titanium dichloride diisopropoxide. | |
EP1461315B1 (en) | Catalytic carbonylation of three and four membered heterocycles | |
US6639087B2 (en) | Kinetic resolution method | |
Gross et al. | Reaction profile of the last step in cytochrome P-450 catalysis revealed by studies of model complexes | |
RU2313531C1 (en) | Method for preparing 1-ethyl-3,4-di-(7-octenyl)-aluminacyclopentane | |
Yamashita | A new synthesis of optically active trans β-amino alcohols by asymmetric ring-opening of symmetrical oxiranes | |
Grenz et al. | Synthesis and application of novel catalytically active polymers containing 1, 4, 7-triazacyclononanesElectronic supplementary information (ESI) available: experimental details. See http://www. rsc. org/suppdata/cc/b1/b105560g | |
Harthun et al. | Proof of chiral dihydride complexes including catalyst and substrate during the bis (phosphinite) rhodium (I)‐catalyzed hydrogenation of dimethyl itaconate | |
RU2183637C2 (en) | Method of combined synthesis of 1-ethyl-2- alkylidenealumacyclopentanes and 1-ethyl-2- methylene-3- alkylalumacyclopentanes | |
Moran et al. | Reactions of diazo compounds with imines. Preliminary communication | |
US11192912B1 (en) | Synthesis of biaryl ketones and biaryl diketones via carbonylative Suzuki-Miyaura coupling reactions catalyzed by bridged bis(N-heterocyclic carbene)palladium(II) catalysts | |
RU2100355C1 (en) | Method for catalytic binding of carbon dioxide | |
KR850000925B1 (en) | Method of Asymmetric Epoxidation | |
RU2245885C1 (en) | Method of jointly preparing 2-alkylidenemagnesiumcyclopentanes and 2-alkyl-3-methylidenemagnesiumcyclopentanes | |
US4628139A (en) | Bis(1,5-cyclooctadiene)Ni(O) catalyst and process for oligomerization of ethylene | |
KR100389459B1 (en) | Production Method of Alkylene Carbonates | |
Matsumoto et al. | An approach to a chiral cycloalkanone-mediated asymmetric epoxidation of stilbene with oxone® | |
RU2191192C1 (en) | Method of synthesis of substituted 1-ethylalumo-cyclopentanes | |
RU2423371C2 (en) | Method of producing 1-ethyl-2,3-dialkyl(phenyl)aluminacyclopent-2-enes | |
RU2342393C2 (en) | METHOD OF OBTAINING 1-ETHYL-1,2,3,3a,4,5,6,7,8,9-DECAHYDROCYCLONONE[b]ALUMINACYCLOPENTANE | |
US6605733B2 (en) | Titanium-containing solid catalyst and process for producing epoxy compound using the same | |
RU2381230C2 (en) | Method of producing tricyclo[4.2.1.02,5]nonane-3-spiro (3'-ethyl-3'-aluminacyclopentane) | |
SU493454A1 (en) | The method of obtaining butene-1 | |
RU2231528C2 (en) | Method for combined preparing 1-ethyl-2-alkyl-3-[1'-ethylalumacyclopent-3'-yl)methyl]-alumacyclopent-2-enes and 1-ethyl-2-[1'-ethylalumacyclopent-3'-yl)methyl]-3-alkylalumacyclopent-2-enes | |
RU2342395C2 (en) | METHOD OF OBTAINING 1-ETHYL-2,3,4,5,6,7,8,9-OCTAHYDRO-1H-CYCLOOCTA-[b]-ALUMINACYCLOPENTANE |