74829-91-7Relevant academic research and scientific papers
Enantioselective nickel-catalyzed reductive coupling of alkynes and imines
Zhou, Chang-Yue,Zhu, Shou-Fei,Wang, Li-Xin,Zhou, Qi-Lin
supporting information; experimental part, p. 10955 - 10957 (2010/09/17)
The nickel-catalyzed reductive coupling of alkynes and imines with Et 2Zn as a reductant by using electron-rich phosphine ligands has been developed, affording various allylic amines with high yields and excellent chemoselectivities. Chiral induction was also achieved in this reductive coupling reaction when a nickel catalyst containing a chiral spiro phosphine ligand was used.
Abnormal Four-Membered Ring Formation in Intramolecular Radicalic Cyclization. High Stability of the Alkyl Radical Substituted with Methylthio and p-Tolylsulfonyl Groups
Ogura, Katsuyuki,Sumitani, Naoko,Kayano, Akio,Iguchi, Hirotaka,Fujita, Makoto
, p. 1487 - 1488 (2007/10/02)
Treatment of 5-iodo-1-(methylthio)-1-(p-tolylsulfonyl)-1-pentene with (n-Bu)3SnH and AIBN gave cyclobutane.This is due to the stability of an intermediary radical attached to methylthio and p-tolylsulfonyl groups.
Reactions of (E)-2-Iodo-1-tosyl-1-alkenes as Useful Synthetic Intermediates
Iwata, Noriyoshi,Morioka, Tetsuro,Kobayashi, Toshifumi,Asada, Takahiro,Kinoshita, Hideki,Inomata, Katsuhiko
, p. 1379 - 1388 (2007/10/02)
(E)-2-Iodo-1-tosyl-1-alkenes readily available by iodosulfonization of 1-alkynes were found to be useful synthons for the regio- and/or stereoselective preparation of 1-tosyl-1-alkynes, 1-tosyl-2-alkynes, (Z)-vinyl and (Z)-allyl sulfones, β-tosyl enamines
Regio- and Stereoselective Synthesis of (E)- and (Z)-Vinylic Sulfones and Their Conversion to the Corresponding Allylic Sulfones
Kobayashi, Toshifumi,Tanaka, Yuhji,Ohtani, Takashi,Kinoshita, Hideki,Inomata, Katsuhiko,Kotake, Hiroshi
, p. 1209 - 1212 (2007/10/02)
(E)- and (Z)-vinilyc sulfones were prepared regio- and stereoselectively from 1-alkenes or 1-alkynes in high yields via iodosulfonization in AcOEt-H2O.The vinylic sulfones thus prepared were converted to the corresponding allylic sulfones by treatment wit
Convenient Methods for the Preparation of Vinylic and Allylic Sulfones from Alkenes, Haloalkanes, and Aldehydes. Stereochemistry of the Conversion of Vinylic Sulfones to the Corresponding Allylic Sulfones
Inomata, Katsuhiko,Sasaoka, Shin-ichi,Kobayashi, Toshifumi,Tanaka, Yuhji,Igarashi, Susumu,et al.
, p. 1767 - 1780 (2007/10/02)
1- or 2-p-Tolylsulfonyl(=tosyl)-1-alkenes, vinylic sulfones, were regioselectively prepared from 1-alkenes via iodosulfonization or sulfonylmercuration and also from 1-haloalkanes by the homologation or unhomologation methods.The vinylic sulfones thus prepared were further converted to the corresponding allylic sulfones under basic conditions.The stereochemistry of this conversion was discussed.One-carbon homologated allylic sulfones were directly obtained from aldehydes in good yields by the reaction with diethyl phenylsulfonylmethylphosphonate and 1,8-diazabicycloundec-7-ene (DBU) under mild conditions.
CONVENIENT METHODS FOR THE PREPARATION OF VINYLIC AND ALLYLIC SULFONES FROM ALKENES
Inomata, Katsuhiko,Kobayashi, Toshifumi,Sasaoka, Shin-ichi,Kinoshita, Hideki,Kotake, Hiroshi
, p. 289 - 292 (2007/10/02)
1 or 2-p-Toluenesulfonyl(=tosyl)-1-alkenes were regioselectively prepared from 1-alkenes via iodosulfonization or sulfonylmercuration, respectively.Conversion of 1-tosyl-1-alkenes to the corresponding allylic sulfones, 1-tosyl-2-alkenes, was achieved by t
