Results 231 to 240 of about 330,962 (287)

Hidden O‐Deglycosylation Activity Triggers O → C Rearrangement for Aryl Di‐C‐Glucoside Formation by the C‐Glycosyltransferase From Fortunella crassifolia

Biotechnology and Bioengineering, EarlyView.
Here, we uncovered an unexpected O‐deglycosylation activity of the C glycosyltransferase (FcCGT), forming phloretin (1) from phloretin 2'‐O‐glucoside (2). In the presence of UDP, FcCGT catalyzes the O→C rearrangement to yield nothofagin (3). Upon additional UDP‐glucose, further C‐glycosylation occurs, forming phloretin 3',5'‐di‐C‐glucoside (4 ...
Tuo Li, Annika J. E. Borg, Leo Krammer, Rolf Breinbauer, Bernd Nidetzky   +4 more
wiley   +1 more source

From Boron to Bismuth: The Pre-transmetalation Complex in the Aryl Transfer. [PDF]

J Am Chem Soc
Faber T, Leutzsch M, Nöthling N, Cornella J.   +3 more
europepmc   +1 more source

Lewis Acid Catalyzed Dual Strain-Release Platform for Transforming Azabicyclo[1.1.0]butanes into Functionalized Azetidines with Donor-Acceptor(D-A) Cyclopropanes and Bicyclo[1.1.0]butanes. [PDF]

Org Lett
Hazra S, Patel M, Mondal S, Ahmed R, Sasmal P, De S, Saha J.   +6 more
europepmc   +1 more source

Visible light-mediated 1,2-difunctionalization reactions involving 4-cyanopyridines. [PDF]

RSC Adv
Raymand P, Farahani A, Doraghi F, Edareh MH, Ghasemi M, Mahdavi M.   +5 more
europepmc   +1 more source

Recent Advances in Transition-Metal-Catalyzed Selective Synthesis of π‑Conjugated Silacycles: A Mini-Review. [PDF]

ACS Omega
Ali SSJ, Das RS, Kumar S, Guha NR.
europepmc   +1 more source

Arylhydrazines: Convenient Homogeneous Reductants for Scalable Cross-Coupling. [PDF]

Angew Chem Int Ed Engl
Kurig N, Cagan DA, Harper KC, Kawamata Y, Blackmond DG, Baran PS.   +5 more
europepmc   +1 more source

Catechol-derived propargyl diol cyclizations with malonyl dichloride: substituent effects on the formation of macrocyclic esters and their hydrochlorinated adducts. [PDF]

RSC Adv
Lefkaritis G, Kourtellaris A, Chronakis N, Georgiades SN.   +3 more
europepmc   +1 more source

Design principles for enantiospecific <i>para</i>- and <i>ortho</i>-[3,3] rearrangements of chiral aryl-allyl ethers.

Org Chem Front
Breinsperger J, Kaiser M, Gärtner P.
europepmc   +1 more source