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Guanidine Chemistry

Chemical and Pharmaceutical Bulletin, 2010
Guanidines are categorized as strong organobases; however, their catalytic utility in organic synthesis has not been discussed thoroughly. The author's group has extensively and systematically studied their potential ability focusing on: 1) modified guanidines as chiral auxiliaries; 2) guanidinium ylides for aziridine formation; 3) the affinity of ...
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Cyclic guanidines. VI. Synthesis of hypoglycemic tricyclic guanidines.

Chemical and Pharmaceutical Bulletin, 1979
Synthesis of linear and angular tricyclic guanidine derivatives, imidazo- or pyrimido-[2, 1-b]- or [1, 2-a] quinazoline derivatives, is described. Cyclization of 2-(ω-chloroalkyl)-4-phenyl-3, 4-dihydroquinazolines (9) gave two isomers and their isolation was troublesome.
A, Kosasayama, K, Higashi, F, Ishikawa
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Chiral Guanidines

Journal of Synthetic Organic Chemistry, Japan, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Tsutomu Ishikawa, Toshio Isobe
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GUANIDINATED CYTOCHROME C [PDF]

Proceedings of the National Academy of Sciences, 1964
T P, HETTINGER, H A, HARBURY
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Cyanobacterial Biofertilizer Production by Guanidine-Producing Enzymes. [PDF]

ACS Synth Biol
Lee H, Sebesta J, Schaedig E, Wu C, Pakrasi HB, Yu J.   +5 more
europepmc   +1 more source

A rapid and accurate guanidine CEST imaging in ischemic stroke using a machine learning approach. [PDF]

Phys Med Biol
Viswanathan M, Yin L, Kurmi Y, Chen Y, Jiang X, Xu J, Afzal A, Zu Z.   +7 more
europepmc   +1 more source

Electrodeficient Diborane (4) Converted into an Extraordinary Proton Sponge. [PDF]

J Phys Chem A
Yáñez M, Montero-Campillo MM, Mó O, Alkorta I.   +3 more
europepmc   +1 more source

Metabolic Origin, Role and Fate of the Denaturant Guanidine. [PDF]

Microb Biotechnol
Danchin A, de Lorenzo V, Nikel PI, You C.   +3 more
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Demethylation of methylguanidine by a stepwise dioxygenase and lyase reaction. [PDF]

Nat Commun
Sinn M, Funck D, Gamer F, Blumenthal C, Kramp C, Hartig JS.   +5 more
europepmc   +1 more source

A 2nd-generation scalable synthesis of the HIV-1 entry inhibitor CJF-III-288 enabled by photoredox catalysis. [PDF]

Chem Commun (Camb)
Nadraws JW, Pokle MS, Smith AB.
europepmc   +1 more source