1. Home
  2. 36f toc

Straightforward Access to Terminally Disubstituted Electron

$ 9.00

4.7 (307) In stock

Selective E to Z isomerization of 1,3-Dienes Enabled by A Dinuclear Mechanism

Gruzman ARIE, PhD, Bar Ilan University, Ramat Gan

Scheme 1. Synthesis of 4-substituted-and 2-substituted-cyclopentenone

π-Stacked Oligomers as Models for Semiconducting Conjugated Organic Materials

Gregory LEITUS, Dr.

Stereochemistry of 1,2-Elimination and Proton-Transfer Reactions

Molecules, Free Full-Text

EAS On Disubstituted Benzenes: The Strongest Electron-Donor Wins

Straightforward Access to Terminally Disubstituted Electron‐Deficient Alkylidene Cyclopent‐2‐en‐4‐ones through Olefination with α‐Carbonyl and α‐Cyano Secondary Alkyl Sulfones - Trifonov - 2021 - European Journal of Organic Chemistry - Wiley Online Library

A Catalytic Dual Isomerization/Allylboration Sequence for the Stereoselective Construction of Congested Secondary Homoallylic Alcohols

Four-membered ring systems - ScienceDirect

PDF) Protective Effect of a Locked Retinal Chromophore Analog

C–H bond activation and sequential addition to two different coupling partners: a versatile approach to molecular complexity - Chemical Society Reviews (RSC Publishing) DOI:10.1039/D2CS00012A

Traceless Stereoinduction for the Enantiopure Synthesis of Substituted-2-Cyclopentenones

π-Stacked Oligomers as Models for Semiconducting Conjugated Organic Materials