Stereoselective Synthesis of (-)-Spicigerolide [PDF]
(-)-Spicigerolide was enantioselectively synthesized from a protected (S)-lactaldehyde. The synthesis of the polyacetylated framework relied on two Zn-mediated stereoselective additions of alkynes to aldehydes as well as a regiocontrolled [3,3 ...
Achmad S. +38 more
core +2 more sources
Re-investigation of the fragmentation of protonated carotenoids by ESI and nanoESI-CID-MS/MS [PDF]
RATIONALE Carotenoids are polyene isoprenoids with an important role in photosynthesis and photoprotection. Their characterization in biological matrices is a crucial subject for biochemical research.
Carnevale Neto, Fausto +5 more
core +2 more sources
Enantioselective Synthesis of (+)-Cephalostatin 1 [PDF]
This Article describes an enantioselective synthesis of cephalostatin 1. Key steps of this synthesis are a unique methyl group selective allylic oxidation, directed C−H hydroxylation of a sterol at C12, Au(I)-catalyzed 5-endo-dig cyclization, and a ...
Fortner, Kevin +3 more
core +1 more source
Effect of Ring Size and Migratory Groups on [1,n] Suprafacial Shift Reactions. Confirmation of Aromatic and Antiaromatic Transition-State Character by Ring-Current Analysis [PDF]
Suprafacial sigmatropic shift reactions of 5-substituted cyclopentadienes, 3-substituted cyclopropenes, and 7-substituted cycloheptatrienes have been studied computationally at the MP2/6-31+G* level for structures and energetics, and using the ...
Clarke, J. +3 more
core +1 more source
A Minimal, Unstrained S-Allyl Handle for Pre-Targeting Diels-Alder Bioorthogonal Labeling in Live Cells [PDF]
The unstrained S-allyl cysteine amino acid was site-specifically installed on apoptosis protein biomarkers and was further used as a chemical handle and ligation partner for 1,2,4,5-tetrazines by means of an inverse-electron-demand Diels-Alder reaction ...
, +6 more
core +4 more sources
Synthesis of Fully Substituted Pyrimidines [PDF]
A novel approach to the synthesis of fully substituted pyrimidine derivatives armed with an oxy-functionalized acetate chain at the ring is described. The manifold uses amidines as the nitrogen source and activated skipped diynes as the electrophilic
García-Tellado, Fernando +2 more
core +2 more sources
Semi-synthesis of vanillin from eugenol can be divided into two step reactions namely, isomerization of eugenol intoisoeugenol, and cleavage oxidation of isomerization product into expected reaction product (vanillin).
Hendra Wijaya +2 more
doaj
Reversal of facial selectivity in a thia-Claisen rearrangement by incorporation of a vinylic bromine substituent [PDF]
Thia-Claisen rearrangements have been carried out using N-benzylpyrrolidine-2-thione and chiral allylic bromides derived from D-mannitol.
Ellwood, AR +3 more
core +1 more source
Cover Picture: Hemin Catalyzed Dealkylative Intercepted [2, 3]‐Sigmatropic Rearrangement Reactions of Sulfonium Ylides with 2, 2, 2‐Trifluorodiazoethane (Adv. Synth. Catal. 10/2020) [PDF]
Xiaojing Yan +4 more
openalex +1 more source
Tracking the Transition from Pericyclic to Pseudopericyclic Reaction Mechanisms Using Multicenter Electron Delocalization Analysis: The [1,3] Sigmatropic Rearrangement [PDF]
Álvaro Pérez‐Barcia +2 more
openalex +1 more source

