The conjugate addition of nitroalkanes to electron-poor alkenes is a widely used process
which only in the late nineties of the last century has efficiently evolved in its asymmetric …

The asymmetric conjugate addition of carbon and heteroatom nucleophiles to nitroalkenes
is a very interesting tool for the construction of highly functionalized synthetic building …

A versatile organocatalyst for the asymmetric conjugate addition of nitroalkanes to enones -
Chemical Communications (RSC Publishing) DOI:10.1039/B511441A Royal Society of …

The crossed-conjugate addition involving the electronwithdrawing group (EWG) of activated
alkenes is considered one of the most important CÀC bond-forming reactions in organic …

Abstract Simple monosulfonated cyclohexane‐1, 2‐diamines are highly enantioselective
organocatalysts for the conjugate addition of ketones to nitro olefins. By focusing on …

Optically active nitroalkanes are versatile precursors for a wide range of useful building
blocks for fine-chemical synthesis. However, only a few effective methods for their …

Catalytic reactions that enable access to different diastereoisomers are important but often
difficult to achieve. One long-standing unsolved challenge is the anti-selective conjugate …

An organocatalytic, enantioselective conjugate addition reaction of nitroalkanes with
nitroolefins has been developed under neat conditions without using an organic solvent …

5-Pyrrolidin-2-yltetrazole is a versatile organocatalyst for the asymmetric conjugate addition
of nitroalkanes to enones. Using this catalyst, this transformation requires short reaction …

Nitroalkenes have often been referred to as" synthetic chameleons" owing to their reactivity,
synthetic utility and biological significance. In the last two decades, the reactivity of …