Cross Coupling Strategies towards the Synthesis of the Streptonigrin CD Moiety

Heterocycles ◽  
1999 ◽  
Vol 51 (4) ◽  
pp. 721 ◽  
Author(s):  
Cedric W. Holzapfel ◽  
Renier Crous ◽  
Catherine Dwyer
2015 ◽  
Vol 80 (19) ◽  
pp. 9410-9424 ◽  
Author(s):  
Kåre B. Jørgensen ◽  
Toni Rantanen ◽  
Thilo Dörfler ◽  
Victor Snieckus

Tetrahedron ◽  
2017 ◽  
Vol 73 (40) ◽  
pp. 5946-5958 ◽  
Author(s):  
Misayo Sera ◽  
Hideya Mizufune ◽  
Tsuyoshi Ueda ◽  
Masahiro Mineno ◽  
Atsuhiko Zanka

Synthesis ◽  
2020 ◽  
Vol 52 (18) ◽  
pp. 2623-2638
Author(s):  
Joshua D. Sieber ◽  
Toolika Agrawal

Metal-catalyzed reductive coupling processes have emerged as a powerful methodology for the introduction of molecular complexity from simple starting materials. These methods allow for an orthogonal approach to that of redox-neutral strategies for the formation of C–C bonds by enabling cross-coupling of starting materials not applicable to redox-neutral chemistry. This short review summarizes the most recent developments in the area of metal-catalyzed reductive coupling utilizing catalyst turnover by a stoichiometric reductant that becomes incorporated in the final product.1 Introduction2 Ni Catalysis3 Cu Catalysis4 Ru, Rh, and Ir Catalysis4.1 Alkenes4.2 1,3-Dienes4.3 Allenes4.4 Alkynes4.5 Enynes5 Fe, Co, and Mn Catalysis6 Conclusion and Outlook


Synthesis ◽  
2019 ◽  
Vol 52 (03) ◽  
pp. 337-352 ◽  
Author(s):  
Lidiia A. Smyshliaeva ◽  
Mikhail V. Varaksin ◽  
Valery N. Charushin ◽  
Oleg N. Chupakhin

Azaheterocyclic derivatives of 1,2-dicarba-closo-dodeca­borane (ortho-carborane) are known to be of particular interest due to numerous plausible applications, particularly, in medicine, materials science, and advanced technologies. Three principal synthetic strategies resulting in azaheterocyclic carboranes, in which boron-enriched and azaheterocyclic fragments are linked to each other, either directly by means of the C–C bonds or through a short spacer (CH2, CH2S, CH2O, etc.), have been outlined. These synthetic approaches are of general character and can be used both individually and in combination to afford promising organoboron clusters of diverse architectures.1 Introduction2 C–C Cross-Coupling Strategies in the Synthesis of Azahetero­cyclic Carboranes3 Carboryne-Based Transformation Strategies4 Condensation Strategies: Reactions of Decaborane B10H14 with Substituted Acetylenes5 Conclusion and Outlook


ChemInform ◽  
2010 ◽  
Vol 26 (30) ◽  
pp. no-no
Author(s):  
F. GUILLIER ◽  
F. NIVOLIERS ◽  
A. GODARD ◽  
F. MARSAIS ◽  
G. QUEGUINER ◽  
...  

2019 ◽  
Vol 2019 (19) ◽  
pp. 3022-3034 ◽  
Author(s):  
Alessandra A. G. Fernandes ◽  
Amanda F. da Silva ◽  
Celso Y. Okada ◽  
Vitor Suzukawa ◽  
Rodrigo A. Cormanich ◽  
...  

2011 ◽  
Vol 13 (14) ◽  
pp. 3588-3591 ◽  
Author(s):  
Cédric Schneider ◽  
Ellen Broda ◽  
Victor Snieckus

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