Concepedia

Synthesis of interesting β-nitrohydrazides through a thiourea organocatalysed aza-Michael addition

Ana Alcaine, Eugenia Marqués‐López, Raquel P. Herrera

RSC Advances · 2014 · 25 citations · 71 references

DOIFull text

Open access

Concepts

Abstract

The synthesis of interesting β-nitrohydrazides, as the target product of our reaction, is reached for the first time under organocatalytic enantioselective conditions.

References

71

Enantioselective Michael Reaction of Malonates to Nitroolefins Catalyzed by Bifunctional Organocatalysts

Tomotaka Okino, Yasutaka Hoashi, Yoshiji Takemoto · Journal of the American Chemical Society · 2003 · 1.4K citations

, , +4

Recent Advances in Asymmetric Organocatalytic 1,4‐Conjugate Additions

Svetlana B. Tsogoeva · European Journal of Organic Chemistry · 2007 · 1.1K citations

, , +9

Enantio- and Diastereoselective Michael Reaction of 1,3-Dicarbonyl Compounds to Nitroolefins Catalyzed by a Bifunctional Thiourea

Tomotaka Okino, Yasutaka Hoashi, Tomihiro Furukawa et al. · Journal of the American Chemical Society · 2004 · 1K citations

, , +12

Highly Enantioselective Conjugate Addition of Nitromethane to Chalcones Using Bifunctional Cinchona Organocatalysts

Benedek Vakulya, Szilárd Varga, Tibor Soós · Organic Letters · 2005 · 979 citations

, , +7

Enantio‐ and Diastereoselective Michael Reaction of 1,3‐Dicarbonyl Compounds to Nitroolefins Catalyzed by a Bifunctional Thiourea.

Tomotaka Okino, Yasutaka Hoashi, Tomihiro Furukawa et al. · ChemInform · 2005 · 863 citations

, , +8