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Other Organometalloids

Arylboronic acid is the most versatile organometalloid due to its efficiency and ready commercial availability. Other organometalloids that can also participate in this copper-promoted cross-coupling reaction are aryltrialkylsiloxanes [51b, 54], aryltrime-thylstannanes [55], triarylbismuths [5,56], arylleads [57], diaryliodonium salts [58a], diethylzinc [58b] and dialkylaluminum chlorides [58c]. [Pg.233]

1 There are over 640 commercially available aryl boronic acids at last count in March 2004. [Pg.238]

2 For recent reviews of Suzuki-Miyaura see (a) A. Suzuki, Modem Arene Chemistry, D. Astruc (Ed), Wdey-VCH, Weinheim, 2002, pp 53-106. (b) S. Kotha, K. Lahiri, D. Kashi-nath. Tetrahedron 2002, 58, 9633-9695. [Pg.238]

4 (a) F. Theil, in Organic Synthesis Highlights V, H. Schmalz, T, Wirth (Eds), Wiley-VCH, Weinheim, 2002, pp 15-21. (b) K. Kunz, [Pg.238]

Hitotsuyanagi, H. Ishikawa, S. Naito, K. Takeya, Tetrahedron Lett. 2003, 44, 5901-5903. [Pg.238]


Chemical Abstracts (Dl) is undoubtedly the most convenient and comprehensive reference source, particularly since 1962 when a section devoted to organometallic and organometalloidal compounds was introduced. Information concerning books, review articles, and conferences is, however, extremely brief, and usually the subject matter of a particular entry must be judged solely from the title. Comparable publications in other languages include Chemisches Informationsdienst (D2) and Refera-tivnyi Zhumal, Khimya. [Pg.474]


See other pages where Other Organometalloids is mentioned: [Pg.125]    [Pg.233]    [Pg.125]    [Pg.233]    [Pg.6090]    [Pg.609]    [Pg.610]    [Pg.96]    [Pg.6089]    [Pg.11]    [Pg.183]    [Pg.32]    [Pg.33]    [Pg.96]    [Pg.183]    [Pg.427]    [Pg.3]    [Pg.17]    [Pg.292]    [Pg.67]   


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