Results 251 to 260 of about 112,449 (386)

Synthesis of 2‐Fluoropyrroles via [4 + 1] Cycloaddition of α,β‐Unsaturated Imines with In Situ‐Generated Difluorocarbene

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
2‐Fluoropyrroles are synthesized via the [4 + 1] cycloaddition of α,β‐unsaturated imines with difluorocarbene, generated in situ from trimethylsilyl 2,2‐difluoro‐2‐(fluorosulfonyl)acetate (TFDA). The α,β‐unsaturated imines are treated with TFDA in the presence of a Proton Sponge catalyst.
Kohei Fuchibe   +2 more
wiley   +1 more source

Diastereoselective Synthesis of Silyl-Substituted Pyrrolidines. [PDF]

open access: yesJ Org Chem
Carboni D   +5 more
europepmc   +1 more source

Synthesis of Diverse β,β‐Diaryl β‐Siloxy Diamines and Application as Organocatalysts

open access: yesEuropean Journal of Organic Chemistry, Accepted Article.
β,β‐Diaryl‐β‐siloxy diamines were developed as a tunable scaffold for structurally diverse diamine‐based organocatalysts. Synthesis was initiated with the reaction of an oxazolidine methyl ester from L‐serine with various Grignard reagents, introducing a wide range of diaryl substituents at the β‐position.
Satoru Arimitsu   +3 more
wiley   +1 more source

Synthesis of Bioorthogonal Mycolic Acids: Chemoselective Reduction of β‐Ketoesters Containing an Alkyne Using the Noyori Catalyst

open access: yesEuropean Journal of Organic Chemistry, Accepted Article.
The asymmetric reduction of β‐ketoesters using the Noyori catalyst is a highly effective synthetic methodology, offering excellent stereocontrol for the preparation of enantiopure b‐hydroxyesters from prochiral substrates in high yields. This reaction has been used in the total synthesis of mycolic acids, which are α‐alkyl, β‐hydroxy fatty acids ...
Paulin Rollando   +5 more
wiley   +1 more source

Removal of C-ring from the CD-ring skeleton of 1 alpha,25-dihydroxyvitamin D-3 does not alter its target tissue metabolism significantly [PDF]

open access: yes, 2007
BOUILLON, R   +11 more
core   +1 more source

Cobalt(I)‐Catalyzed E‐Selective Hydroalkynylation of Terminal Alkynes or Internal Alkynes with Silyl‐Substituted Terminal Alkynes

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
The cross‐hydroalkynylation of silyl‐substituted terminal alkynes, acting as CH‐donor alkynes, with aryl‐ or alkyl‐substituted terminal alkynes, acting as acceptor alkynes, is described. Cross‐hydroalkynylation with internal alkynes acting as acceptor alkynes is successful when at least one aryl substituent is present.
Sebastian M. Weber, Gerhard Hilt
wiley   +1 more source

Ketone-Assisted Alkoxysilane Condensation to Form Siloxane Bonds. [PDF]

open access: yesMolecules
Rubinsztajn S   +4 more
europepmc   +1 more source

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