Results 1 to 10 of about 14,649 (249)

Enantioselective Synthesis of (+)-Auriculatol A. [PDF]

J Am Chem Soc
A total synthesis of the grayanane diterpenoid (+)-auriculatol A is reported. The synthesis features a convergent coupling strategy that joins two fragments by a vinylogous Mukaiyama aldol-type reaction and then constructs the 7-membered ring by a nickel-catalyzed eno-late alkenylation.
Thompson JK, Youngblood KC, Teh YHS, Farley CM, Zhang Z, Virgil SC, Reisman SE.   +6 more
europepmc   +4 more sources

Enantioselective synthesis of chiroplasmonic helicoidal nanoparticles by nanoconfinement in chiral dielectric shells [PDF]

Nature Communications
Helicoid metal nanoparticles with intrinsic chirality have unveiled tailorable properties and unlocked many chirality-related applications across various fields.
Xiaoxi Luan, Yu Tian, Fengxia Wu, Lu Cheng, Minghua Tang, Xiali Lv, Haili Wei, Xiaodan Wang, Fenghua Li, Guobao Xu, Wenxin Niu   +10 more
doaj   +2 more sources

Photoenzymatic enantioselective synthesis of fluorinated amides with remote stereocenter [PDF]

Nature Communications
Fluorinated compounds are scarce in nature, albeit they are in high demand in pharmaceuticals, agrochemicals, and materials. Fluorinated amides serve as prevalent structural motifs in pharmaceuticals and bioactive molecules.
Chaoqun Huang, Xuerui Jin, Zhenyu Liu, Can Cui, Yang Zhang, Binju Wang, Chun Zhang, Jianqiang Feng, Dawen Niu, Yunzi Luo   +9 more
doaj   +2 more sources

Enantioselective Synthesis of Sealutomicin C. [PDF]

J Am Chem Soc
The sealutomicins are a family of anthraquinone antibiotics featuring an enediyne (sealutomicin A) or Bergman-cyclized aromatic ring (sealutomicins B – D). Herein we report the development of an enantioselective organocatalytic method for the synthesis of dihydroquinolines and the use of the developed method in the total synthesis of sealutomicin C ...
Astle SM, Guggiari S, Frost JR, Hepburn HB, Klauber DJ, Christensen KE, Burton JW.   +6 more
europepmc   +4 more sources

Enantioselective Synthesis of N1999A2. [PDF]

ChemInform, 2006
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Nan, Ji, Hardwin, O'Dowd, Brad M, Rosen, Andrew G, Myers   +3 more
openaire   +3 more sources

Enantioselective Synthesis of (+)‐Majusculone (I). [PDF]

ChemInform, 2007
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Douglass F, Taber, M Inthikhab, Sikkander, Pierre H, Storck   +2 more
openaire   +2 more sources

Enantioselective [4+2] Annulation to the Concise Synthesis of Chiral Dihydrocarbazoles

iScience, 2020
Summary: A highly efficient phosphine-catalyzed enantioselective [4 + 2] annulation of allenoates with 3-nitroindoles or 3-nitrobenzothiophenes has been developed.
Haiyang Wang, Qingdong Hu, Mingxu Wang, Chang Guo   +3 more
doaj   +1 more source

Enantioselective Synthesis of a New Non-Natural Gabosine

Molecules, 2021
The preparation of a new non-natural gabosine is reported, in which the chirality is transferred from the toluene’s biotransformed metabolite (1R,2S)-3-methylcyclohexa-3.5-diene-1,2-diol.
Maximiliano Colobbio, Enrique Pandolfi, Valeria Schapiro   +2 more
doaj   +1 more source

Catalytic enantioselective reductive alkynylation of amides enables one-pot syntheses of pyrrolidine, piperidine and indolizidine alkaloids

Nature Communications, 2023
The primary objective in synthetic organic chemistry is to develop highly efficient, selective, and versatile synthetic methodologies, which are essential for discovering new drug candidates and agrochemicals. In this study, we present a unified strategy
Fang-Fang Xu, Jin-Quan Chen, Dong-Yang Shao, Pei-Qiang Huang   +3 more
doaj   +1 more source

Challenging Atroposelective C–H Arylation

SynOpen, 2020
Atropisomeric molecules are privileged scaffolds, not only as ligands for asymmetric synthesis, but also as biologically active products and advanced materials.
Joanna Wencel-Delord, Françoise Colobert   +1 more
doaj   +1 more source