Metal-catalyzed highly Markovnikov-type selective hydrofunctionalization of terminal alkynes
provides a straightforward and atom-economical route to access 1, 1-disubstituted alkenes …

An important first step in making organic reactions more environmentally benign by design
requires processes that are, to a first approximation, simple additions with anything else …

The demand for new chemicals spanning the fields of health care to materials science
combined with the pressure to produce these substances in an environmentally benign …

A stereodivergent reductive coupling reaction between allylic carbonates and vinyl triflates
to furnish both E‐and Z‐configured 1, 4‐dienes has been achieved by visible‐light‐induced …

We have developed catalytic anti-Markovnikov hydroallylation of terminal and functionalized
internal alkynes. In this article, we describe the development of the reaction, exploration of …

Here, we reported a cobalt-hydride-catalyzed Markovnikov-type hydroallylation of terminal
alkynes with allylic electrophile to access valuable and branched skipped dienes (1, 4 …

Nickel-catalyzed intermolecular benzylation and heterobenzylation of unactivated alkenes to
provide functionalized allylbenzene derivatives are described. A wide range of both the …

A Convenient Synthetic Route to [CpRu(CH3CN)3]PF6 | Organometallics Recently Viewed
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Achieving divergent synthesis from the same substrates quickly to generate different
products remains an attractive objective in synthetic chemistry and the medicinal industry …

A wide variety of diynols containing tertiary, secondary, and primary propargylic alcohols
undergo a cycloisomerization reaction to form dienones and dienals in the presence of a …