Results 111 to 120 of about 5,133 (208)

3-Azetidinylpiperidine-4-alkylidenemalononitrile and Related Building Blocks. [PDF]

Org Lett
Sanfiel JM, McCabe AT, Nilova A, Graf SL, Boyn JN, Grenning AJ.   +5 more
europepmc   +1 more source

Nucleophilic Ring Opening of Aziridine and Azetidine Derivatives in Liquid Sulfur Dioxide

Aziridine and azetidine moieties are important small ring N-heterocycles in organic synthesis due to their biological and pharmacological properties and synthetic potential as a building blocks.
Lugiņina, Jevgeņija, Turks, Māris
core  

Triplet Energy Transfer-Driven Intermolecular [2+2] Photocycloaddition of Acyclic Imines and Indoles: Facile Access to Azetidine-Fused Indolines. [PDF]

Adv Sci (Weinh)
Yang G, Han Z, Zhang H, Cui X.
europepmc   +1 more source

Editorial: Recent advances in synthesizing and utilizing nitrogen-containing heterocycles

Frontiers in Chemistry
Takashi Ohshima, Hsyueh-Liang Wu, Hyun-Joon Ha   +2 more
doaj   +1 more source

4″-Methyl-<i>S</i>-Adenosyl-l-Methionines Are Substrates for 4-Methylazetidinecarboxylic Acid Synthases. [PDF]

ACS Chem Biol
Nagano N, Kiuchi K, Minato A, Sato S, Moriwaki Y, Müller R, Eguchi T, Kudo F.   +7 more
europepmc   +1 more source

Synthesis and functionalization of azetidine‐containing small macrocyclic peptides

Cyclic peptides are increasingly important structures in drugs but their development can be impeded by difficulties associated with their synthesis. Here, we introduce the 3‐aminoazetidine (3‐AAz) subunit as a new turn‐inducing element for the efficient ...
Stefan Roesner (2151052), Rebecca Notman (761166), Sam Spring (18177154), Ina Wilkening (2156464), Michael Shipman (1294968), Guy Clarkson (1269390), Ann Dixon (16632030), George Saunders (18177151), Eleanor Jayawant (10656704)   +8 more
core   +1 more source

Correction to "Discovery and Mechanism of a Diiron Enzyme in Ethylidene Azetidine Formation". [PDF]

J Am Chem Soc
Shen Y, Zheng YC, Palacios PM, Wang K, Maggiolo AO, Guo Y, Chang WC.   +6 more
europepmc   +1 more source

Noncatalytic [2+2] Cycloaddition Providing Donor-Acceptor Type 2-Azetines Featuring the 2-Aminophenyl Groups. [PDF]

Chemistry
Morisaki M, Abe R, Ito S.
europepmc   +1 more source

S-Adenosyl-d-Methionine as a Non-Physiological Substrate for a Wide Range of SAM-Dependent Enzymes. [PDF]

Chembiochem
Germer P, Gericke L, Koeppl LH, Zou Z, Jockmann E, Kuge M, Zoller K, Herrmann H, Fuderer R, Mohr MKF, Bartels A, Oral G, Lukat P, Layer G, Müller M, Blankenfeldt W, Barra L, Andexer JN.   +17 more
europepmc   +1 more source

The Chemistry of Azetidines

Journal of Synthetic Organic Chemistry, Japan, 1972
openaire   +2 more sources