Results 51 to 60 of about 108,077 (187)
Retro-allylation of bulky gallium homoallylic alkoxides occurs to generate (Z)- and (E)-crotylgallium reagents stereospecifically, starting from erythro- and threo-homoallylic alcohols, respectively.
Hideki Yorimitsu (1393411) +3 more
core +1 more source
Asymmetric Iron‐Catalyzed Vicinal C(sp3)─H Diamination of Carboxylic Acids
An iron‐catalyzed vicinal α,β‐C(sp3)─H diamination of readily available carboxylic acids furnishes chiral α,β‐diamino acids in a single pot with high regio‐, diastereo‐, and enantioselectivity (up to >20:1 dr and >99% ee). ABSTRACT The direct construction of chiral 1,2‐diamines through the stereoselective functionalization of two vicinal C(sp3)─H bonds
Bing Zhou +5 more
wiley +2 more sources
The Expanding Role of Diazirines in Synthetic Methodology
Beyond their established role in photoaffinity labeling, diazirines have emerged as versatile reagents in synthetic chemistry. This review highlights their dual reactivity as carbene and nitrogen‐transfer precursors, showcasing mechanistic insights and diverse applications in cyclopropanations, cycloadditions, skeletal editing, amination, heterocycle ...
Viktor Savic +3 more
wiley +1 more source
Iodoetherification of homoallylic alcohols : A stereoselective approach to tetrahydrofurans
Iodoetherification of homoallylic alcohols proceeds efficiently and with high levels of stereoselection by a 5-endo-trig process when anhydrous acetonitrile is used as the ...
Duncan Shaw +11 more
core +1 more source
We describe the application of an amidoxime as catalyst in the synthesis of homoallylic alcohols from the allylation reaction of aldehydes with different features using potassium allyltrifluoroborate. The reaction was conducted with a catalytic amount of
Dmistocles de Andrade +2 more
doaj +1 more source
Total Synthesis of Chaxalactin B, a Rare 22‐Membered Macrolactone
The first total synthesis of the antibacterial 22‐membered macrolactone chaxalactin B has been accomplished in 23 steps (longest linear sequence). Key transformations feature a stereoselective Marshall propargylation, a Suzuki–Miyaura coupling for the assembly of the main C1–C9 and C10–C25 fragments, and a late‐stage Shiina macrolactonization ...
Ophélie Montiège +7 more
wiley +1 more source
Highly Diastereoselective Preparation of Homoallylic Alcohols Containing Two Contiguous Quaternary Stereocenters in Acyclic Systems from Simple Terminal ...
Noga Gilboa (2303011) +2 more
core +2 more sources
Catalytic Enantioselective Epoxidation of Homoallylic Alcohols by Chiral Zirconium Complexes. [PDF]
AbstractFor Abstract see ChemInform Abstract in Full Text.
Takahiro, Okachi +2 more
openaire +2 more sources
Advancements in Carbohydrate Scaffold Synthesis: Exploring Prins Cyclization Methodology
The synthesis of natural and unconventional compounds with carbohydrate structures is of great interest to glycochemists due to their vital biological roles. In recent years, there has been significant progress in developing direct and indirect synthetic
Sateesh Dubbu, Santhi Jampani
doaj +1 more source
Reduction of allylic sulfones with samarium diiodide gives allylsamarium species which react in situ with carbonyl compounds, yielding homoallylic alcohols.
Clayden, Jonathan, Julia, Marc
core +1 more source

