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Kasatkin, Aleksandr, Nakagawa, Takashi, Okamoto, Sentaro, Sato, Fumie (1995) New, Efficient Method for the Synthesis of Allyltitanium Compounds from Allyl Halides or Allyl Alcohol Derivatives via Oxidative Addition. A Highly Efficient and Practical Synthesis of Homoallyl Alcohols. Journal Of The American Chemical Society, 117 (13) 3881-3882 doi:10.1021/ja00118a030

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Reference TypeJournal (article/letter/editorial)
TitleNew, Efficient Method for the Synthesis of Allyltitanium Compounds from Allyl Halides or Allyl Alcohol Derivatives via Oxidative Addition. A Highly Efficient and Practical Synthesis of Homoallyl Alcohols
JournalJournal Of The American Chemical Society
AuthorsKasatkin, AleksandrAuthor
Nakagawa, TakashiAuthor
Okamoto, SentaroAuthor
Sato, FumieAuthor
Year1995 (April)Volume117
Issue13
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja00118a030Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID1489149Long-form Identifiermindat:1:5:1489149:4
GUID0
Full ReferenceKasatkin, Aleksandr, Nakagawa, Takashi, Okamoto, Sentaro, Sato, Fumie (1995) New, Efficient Method for the Synthesis of Allyltitanium Compounds from Allyl Halides or Allyl Alcohol Derivatives via Oxidative Addition. A Highly Efficient and Practical Synthesis of Homoallyl Alcohols. Journal Of The American Chemical Society, 117 (13) 3881-3882 doi:10.1021/ja00118a030
Plain TextKasatkin, Aleksandr, Nakagawa, Takashi, Okamoto, Sentaro, Sato, Fumie (1995) New, Efficient Method for the Synthesis of Allyltitanium Compounds from Allyl Halides or Allyl Alcohol Derivatives via Oxidative Addition. A Highly Efficient and Practical Synthesis of Homoallyl Alcohols. Journal Of The American Chemical Society, 117 (13) 3881-3882 doi:10.1021/ja00118a030
In(1995, April) Journal Of The American Chemical Society Vol. 117 (13) American Chemical Society (ACS)

See Also

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Ono, Naoya, Tsuboi, Mie, Okamoto, Sentaro, Tanami, Tohru, Sato, Fumie (1992) Synthesis of Allyl Ester of Prostaglandin E and the Conversion of the Allyl Ester Moiety into Carboxylic Acid by Chemical Method. A Highly Practical Synthesis of Natural PGE1and Limaprost. Chemistry Letters, 21 (10). 2095-2098 doi:10.1246/cl.1992.2095
Okamoto, Sentaro, Kasatkin, Aleksandr, Zubaidha, P. K., Sato, Fumie (1996) Intramolecular Nucleophilic Acyl Substitution Reactions Mediated by XTi(O-i-Pr)3(X = Cl, O-i-Pr)/2i-PrMgBr Reagent. Efficient Synthesis of Functionalized Organotitanium Compounds from Unsaturated Compounds. Journal Of The American Chemical Society, 118 (9) 2208-2216 doi:10.1021/ja953497z
Teng, Xin, Takayama, Yuuki, Okamoto, Sentaro, Sato, Fumie (1999) Development of a Chiral Propionaldehyde Homoenolate Equivalent Which Reacts with Imines with Excellent Stereoselectivity:  Efficient and Practical Synthesis of Optically Active γ-Amino Carbonyl Compounds. Journal Of The American Chemical Society, 121 (50) 11916-11917 doi:10.1021/ja9933487
Okamoto, Sentaro, Subburaj, Kandasamy, Sato, Fumie (2000) Highly Stereocontrolled Synthesis of Carbacyclin from Acyclic Starting Materials via Ti(II)-Mediated Tandem Cyclization. Journal Of The American Chemical Society, 122 (45) 11244-11245 doi:10.1021/ja002974x
Fukuhara, Kohki, Okamoto, Sentaro, Sato, Fumie (2003) Asymmetric Synthesis of Allyl- and α-Allenylamines from Chiral Imines and Alkynes via (η2-Imine)Ti(O-i-Pr)2Complexes. Organic Letters, 5. 2145-2148 doi:10.1021/ol034599u
MUKAIYAMA, T., HARADA, T. (1982) ChemInform Abstract: AN EFFICIENT SYNTHESIS OF HOMOALLYL ALCOHOLS BY THE REACTION OF ALLYL HALIDES WITH CARBONYL COMPOUNDS IN THE PRESENCE OF METALLIC TIN. Chemischer Informationsdienst, 13 (21) doi:10.1002/chin.198221174
Kitano, Yasunori, Matsumoto, Takashi, Okamoto, Sentaro, Shimazaki, Toshiyuki, Kobayashi, Yuichi, Sato, Fumie (1987) A Highly Efficient Synthesis of Prostaglandin ω-Chain Precursors. Chemistry Letters, 16 (8). 1523-1526 doi:10.1246/cl.1987.1523
Okude, Yoshitaka, Hirano, Shigeo, Hiyama, Tamejiro, Nozaki, Hitosi (1977) Grignard-type carbonyl addition of allyl halides by means of chromous salt. A chemospecific synthesis of homoallyl alcohols. Journal Of The American Chemical Society, 99 (9) 3179-3181 doi:10.1021/ja00451a061
Okamoto, Sentaro, Teng, Xin, Fujii, Shintaro, Takayama, Yuuki, Sato, Fumie (2001) An Allyltitanium Derived from Acrolein 1,2-Dicyclohexylethylene Acetal and (η2-propene)Ti(O-i-Pr)2as a Chiral Propionaldehyde Homoenolate Equivalent that Reacts with Imines with Excellent Stereoselectivity. An Efficient and Practical Access to Optically Active γ-Amino Carbonyl Compounds. Journal Of The American Chemical Society, 123 (15) 3462-3471 doi:10.1021/ja004140k
Okamoto, Sentaro, Iwakubo, Masayuki, Kobayashi, Katsushige, Sato, Fumie (1997) Efficient and Practical Method for Synthesizing N-Heterocyclic Compounds Using Intramolecular Nucleophilic Acyl Substitution Reactions Mediated by Ti(O-i-Pr)4/2i-PrMgX Reagent. Synthesis of Quinolones, Pyrroles, Indoles, and Optically Active N-Heterocycles Including Allopumiliotoxin Alkaloid 267A. Journal Of The American Chemical Society, 119 (30) 6984-6990 doi:10.1021/ja970810j
Mukaiyama, Teruaki, Harada, Taira (1981) AN EFFICIENT SYNTHESIS OF HOMOALLYL ALCOHOLS BY THE REACTION OF ALLYL HALIDES WITH CARBONYL COMPOUNDS IN THE PRESENCE OF METALLIC TIN. Chemistry Letters, 10 (11). 1527-1528 doi:10.1246/cl.1981.1527
 
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