Silver in Organic Chemistry

  • ID: 1415182
  • Book
  • 402 Pages
  • John Wiley and Sons Ltd
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The first authoritative book on using silver cations in organic chemistry for catalysis and more!

With more sophisticated catalytic methodologies fueling a resurgence in the study of cation–based chemistry, gold and platinum have stepped to the fore as the unique agents used to create new chemical reactions. Although these metals have become a primary focus of researchers in the field, another coinage metal that is often overlooked but is as powerful as the others is silver, a far less costly alternative to gold and platinum in aiding the development of new reactions.

Making a strong case for the use of silver as a catalyst and structural element in organometal constructs, this authoritative book is the first to explore the benefits of using silver in organic chemistry by taking a close look at silver s unique reactivity and structural characteristics for the development of new methods and materials. Silver in Organic Chemistry is:

  • The first book to address catalysis using silver, whose use in organic chemistry is on the verge of exploding
  • A resource for researchers wishing to do chemistry with silver cations, an area that stands in the shadow of gold chemistry, but still glistens, demonstrating that all that glitters is not gold sometimes it s silver!
  • A guide for first attempts in working with silver cations
  • Edited by a very well–respected, highly visible authority in this field

Silver in Organic Chemistry promotes further scientific discussion by offering important new ways to examine the future possibilities of an emerging field. By elevating the importance of silver chemistry, this thought–provoking guide illustrates how this versatile metal can become an increasingly significant player in opening the door to new catalytic organic reactions and new organometal materials.

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1 Silver Alkyls, Alkenyls, Aryls, and Alkynyls in Organic Synthesis (Rebecca H. Pouwer and Craig M. Williams).

1.1 Introduction.

1.2 Csp3–Ag.

1.3 Csp2–Ag.

1.4 Csp–Ag.

1.5 Conclusion.


2 Cycloaddition Reactions (Alex M. Szpilman and Erick M. Carreira).

2.1 Introduction.

2.2 [2+2] Cycloadditions.

2.3 [3+2] Cycloadditions.

2.4 [3+3] Cycloadditions.

2.5 [4+2] Cycloadditions.

2.6 Concluding Remarks.


3 Sigmatropic Rearrangements and Related Processes Promoted by Silver (Jean–Marc Weibel, Aurélien Blanc, and Patrick Pale).

3.1 Introduction.

3.2 Wolff and Arndt Eistert Rearrangements and Related Reactions.

3.3 Ring Rearrangements.

3.4 [3,3]–Sigmatropic Rearrangements.

3.5 [2,3]–Sigmatropic Rearrangements.

3.6 [1,2]–Sigmatropic Rearrangements.

3.7 Miscellaneous.

3.8 Conclusion.


4 Silver(I)–Mediated Electrocyclic Processes (Tina N. Grant and Frederick G. West).

4.1 Introduction.

4.2 Nucleophilic Trapping of Cationic Intermediates.

4.3 The Silver(I)–Promoted Nazarov Reaction.

4.4 Concluding Remarks.


5 Silver–Catalyzed Cycloisomerization Reactions (Philippe Belmont).

5.1 Introduction.

5.2 Cycloisomerization of C=O onto C=C=C.

5.3 Cycloisomerization of C=O onto C C.

5.4 Cycloisomerization of C=N onto C=C=C.

5.5 Cycloisomerization of C=N onto C C.

5.6 Ene Yne Cycloisomerization: C=C onto C C.

5.7 Other Transformations.

5.8 Conclusion.


6 Silver–Catalyzed Nitrene Transfer Reactions (Zigang Li, David A. Capretto, and Chuan He).

6.1 Introduction.

6.2 Aziridination.

6.3 Sulfide and Sulfoxide Imination.

6.4 Amidation.

6.5 Conclusion.


7 Silver–Catalyzed Silylene Transfer (Tom G. Driver).

7.1 Introduction.

7.2 Reactivity and Attributes of Metal Silylenoids and Silylmetal Complexes.

7.3 Silacyclopropanes as Important Synthetic Intermediates.

7.4 Silver–Mediated Transfer of Di–tert–Butylsilylene to Olefins.

7.5 Silver–Mediated Transfer of Di–tert–Butylsilylene to Acetylenes.

7.6 Silver–Mediated Transfer of Di–tert–Butylsilylene to Carbonyl Compounds.

7.7 Silver–Mediated Transfer of Di–tert–Butylsilylene to Imines.

7.8 Silver–Mediated Di–tert–Butylsilylene Insertion into C O Bonds.

7.9 Conclusion.


8 Silver Carbenoids (Carl J. Lovely).

8.1 Introduction.

8.2 Wolff Rearrangement.

8.3 Carbene Transfer Reactions to Bonds.

8.4 Formation and Reactions of Ylides.

8.5 C H Insertion.

8.6 N H Insertion.

8.7 Ring Expansion Reactions.

8.8 Intermediacy of Silver Carbenes.

8.9 Miscellaneous Reactions Involving Silver Carbenoids.

8.10 Summary.



9 Aldol and Related Processes (Masanori Kawasaki and Hisashi Yamamoto).

9.1 Introduction.

9.2 Allylation Reaction Using Allyltributyltin.

9.3 Allylation Reaction Using Allylsilanes.

9.4 Aldol Reaction Using Tin Enolates.

9.5 Aldol Reaction Using Silyl Enol Ethers.

9.6 Mannich Reaction.

9.7 Nitrosoaldol Reaction.

9.8 Aldol Reaction with Azodicarboxylate.

9.9 Conclusion.


10 Coupling Reactions Promoted by Silver (Jean–Marc Weibel, Aurélien Blanc, and Patrick Pale).

10.1 Introduction.

10.2 sp3 sp3 Coupling Reactions Promoted by Silver Salts.

10.3 sp3 sp2 Coupling Reactions Promoted by Silver Salts.

10.4 sp3 sp Coupling Reactions Promoted by Silver Salts.

10.5 sp2 sp2 Coupling Reactions Promoted by Silver Salts.

10.6 sp2 sp Coupling Reactions Promoted by Silver Salts.

10.7 sp sp Coupling Reactions Promoted by Silver Salts.

10.8 Conclusion.


11 Supramolecular Chemistry of Silver (Wei–Yin Sun, Zheng–Shuai Bai, and Jin–Quan Yu).

11.1 Introduction.

11.2 Cage–Like Complexes.

11.3 Tube–Like Compounds.

11.4 Polycatenanes with Silver(I).

11.5 Polyrotaxanes with Silver(I).

11.6 Silver(I) Coordination Polymers with Specific Topology.

11.7 Conclusion.



12 A Critical Comparison: Copper, Silver, and Gold (A. Stephen K. Hashmi).

12.1 Introduction.

12.2 Reactions Catalyzed by Copper, Silver, or Gold.

12.3 Reactions Catalyzed by Silver or Gold.

12.4 Reactions Catalyzed by Copper or Silver.

12.5 Conclusion.



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Michael Harmata
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