-
Albert Jakob Eschenmoser (5
August 1925 – 14 July 2023) was a
Swiss organic chemist, best
known for his work on the
synthesis of
complex heterocyclic...
- form a γ,δ-unsaturated amide. This was
developed by
Albert Eschenmoser in 1964.
Eschenmoser-Claisen
rearrangement was used as a key step in the
total synthesis...
- The
Eschenmoser fragmentation,
first published in 1967, is the
chemical reaction of α,β-epoxyketones (1) with aryl
sulfonylhydrazines (2) to give alkynes...
- In
organic chemistry,
Eschenmoser's salt (named for
Albert Eschenmoser) is the ionic,
organic compound [(CH3)2NCH2]I. It is the
iodide salt of the dimethylaminomethylene...
-
collaborating research groups of
Robert Burns Woodward at
Harvard and
Albert Eschenmoser at ETH in 1972. The
accomplishment required the
effort of no less than...
- The
Eschenmoser sulfide contraction is an
organic reaction first described by
Albert Eschenmoser for the
synthesis of 1,3-dicarbonyl
compounds from a thioester...
- ketones,
these hydrazones parti****te in the
Shapiro reaction and the
Eschenmoser–Tanabe fragmentation. 2,4,6-Triisopropylbenzenesulfonylhydrazide is a...
-
cycloisomerization ring
closure reaction,
which was the key step in the
Eschenmoser / ETH Zürich
vitamin B12
total synthesis. The
isosbestic points provide...
-
mechanisms for proto-metabolism
proposed by the
Eschenmoser and
Sutherland groups.
Research from the
Eschenmoser group suggested that
interactions between HCN...
- (10): 357–367. doi:10.1007/BF02167631. PMID 13116962. S2CID 44195550.
Eschenmoser, Albert; Arigoni,
Duilio (December 2005). "Revisited
after 50 Years:...
