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The Stille reaction /
| Tác giả chính: | |
|---|---|
| Tác giả khác: | , |
| Định dạng: | Printed Book |
| Ngôn ngữ: | English |
| Được phát hành: |
New York :
J. Wiley,
c1998.
|
| Những chủ đề: | |
| Truy cập trực tuyến: | http://www.loc.gov/catdir/bios/wiley041/98039154.html http://www.loc.gov/catdir/description/wiley032/98039154.html http://www.loc.gov/catdir/toc/onix02/98039154.html |
| LEADER | 03874pam a2200277 a 4500 | ||
|---|---|---|---|
| 008 | 980804s1998 nyua b 001 0 eng | ||
| 010 | |a 98039154 | ||
| 020 | |a 0471312738 (pbk. : alk. paper) | ||
| 082 | 0 | 0 | |a 547/.2 |2 21 |
| 100 | 1 | |a Farina, Vittorio. | |
| 245 | 1 | 4 | |a The Stille reaction / |c Vittorio Farina and Venkat Krishnamurthy, William J. Scott. |
| 260 | |a New York : |b J. Wiley, |c c1998. | ||
| 300 | |a ix, 657 p. : |b ill. ; |c 23 cm. | ||
| 504 | |a Includes bibliographical references (p. 633-652) and index. | ||
| 505 | |a Mechanistic considerations, regiochemistry and stereochemistry. -- Scope and limitations: the electrophile. -- Alkenyl Halides. -- Aryl and Heterocyclic Halides. -- Acyl Chlorides. -- Allylic, Benzylic, and Propargylic Electrophiles. -- Alkenyl Sulfonates and Other Electrophiles. -- Aryland Heterocyclic Sulfonates and Other Derivatives. -- Miscellaneous Electrophiles. -- Scope and limitations: the stannane. -- Alkylstannanes. -- Alkenylstannes. -- Aryl and Heterocyclic Stannanes. -- Alkynylstannanes. -- Allylstannanes. -- Other Stannanes. -- Carbonylative couplings. -- Alkenyl Halides. -- Aryl and Heterocyclic Halides. -- Allylic and Benzylic Halides. -- Alkenyl Sulfonates. -- Aryl and Heterocyclic Sulfonates. -- Miscellaneous Substrates. -- Complex synthetic sequences involving tin-to-palladium (ii) metathesis steps. -- Side reactions. -- Homocoupling Reactions. -- Transfer of "Nontransferable" Ligands. -- Destannylation. -- Cine Substitution. -- Phosphorus-to-Palladium Aryl Migration. -- Electrophile Reduction. -- Product Isomerization. -- Miscellaneous Side Reactions. -- Comparison with other methods. -- Experimental conditions. -- The Stannane: Preparation and Handling. -- Alkenyl and Aryl Triflates. -- Choice of Nontransferable Ligands. -- Choice of Catalyst and Ligands. -- Choice of Solvent. -- Additives. -- Workup: Removal of Tin Halides. -- Experimental procedures. -- Trimethyl([3-(Cyclohexen-1-yl)-2-Propynyl)silane [Cross-Coupling of a Vinyl Halide with an Alkynylstannane Using Pd(PPh_3)_2Cl_2]. -- 4-tert Butyl-1-Vinylcyclohexene [Cross-Coupling of a Vinyl Triflate with a Vinylstannane Using Pd(PPh_3)_4 and LiCl]. -- 1-(4-Methoxyphenyl)-4-tert-Butylcyclohexene [Cross-Coupling of a Vinyl Triflate with an Arylstannane Using Pd_2(dba)_3 and AsPh_3]. -- 3-Methyl-2-(4-Tolyl)-2-Cyclopentenone [Cross-Coupling of an Unreactive Alkenyl Halide under "Modified" Conditions Using Pd(PhCN)_2Cl_2 AsPh_3, and Cul as Cocatalyst]. -- 1-(4-Nitrophenyl)-2-Propenone (Cross-Coupling of an Acid Chloride with an Arylstannane). -- 4-Allylacetophenone [Cross-Coupling of an Aryl Triflate under Mild Conditions using Tri(2-Furyl)Phosphine as Ligand. -- 8-(Trimethylstannyl)Quinoline (Preparation of an Arylstannane by Cross-Coupling and Aryl Triflate with Hexamethyldistannane). -- 4-(tert-Butyl-1-Vinylcyclohexen-1-Yl)-2-Propenone [Carbonylative Cross-Coupling of an Alkenyl Triflate with an Alkenylstannane using Pd(PPh_3)_4 and LiCl]. -- (E)-1-(4-Methoxphenyl)-3-Phenyl-2-Propenone [Carbonylative Cross-Coupling of an Aryl Triflate with an Alkenylstannane using Pd(dppf)Cl_2 and LiCl]. -- Tubular survey. -- Tables. -- References. | ||
| 650 | 0 | |a Stille reaction. | |
| 700 | 1 | |a Krishnamurthy, Venkat. | |
| 700 | 1 | |a Scott, William Johnston, | |
| 856 | 4 | 2 | |u http://www.loc.gov/catdir/bios/wiley041/98039154.html |
| 856 | 4 | 2 | |u http://www.loc.gov/catdir/description/wiley032/98039154.html |
| 856 | 4 | |u http://www.loc.gov/catdir/toc/onix02/98039154.html | |
| 942 | |c BK | ||
| 906 | |a 7 |b cbc |c orignew |d 1 |e ocip |f 19 |g y-gencatlg | ||
| 955 | |a pc19 RUSH to ja00 08-05-98; jd99 to SHED 08-05-98; je14 08-11-98; jk00 10-26-98; CIP ver. jk15 10-30-98 | ||
| 999 | |c 122248 |d 122248 | ||
| 952 | |0 0 |1 0 |4 0 |6 547_200000000000000_FAR_S |7 0 |9 135354 |a CHE |b CHE |c ST1 |d 2018-02-18 |e 1 |g 8426.88 |i 6647 |l 0 |o 547.2 FAR/S |p CHE6647 |r 2018-06-26 |v 11704.00 |w 2018-06-26 |y BK | ||