112213-42-0Relevant articles and documents
Catalytic Enantioselective Allylations of Acetylenic Aldehydes via 2-Propanol-Mediated Reductive Coupling
Brito, Gilmar A.,Della-Felice, Franco,Luo, Guoshun,Burns, Alexander S.,Pilli, Ronaldo A.,Rychnovsky, Scott D.,Krische, Michael J.
, p. 4144 - 4147 (2018)
Cyclometalated π-allyliridium C,O-benzoates modified by (S)-SEGPHOS or (S)-Cl,OMe-BIPHEP catalyze enantioselective 2-propanol-mediated reductive couplings of diverse nonmetallic allyl pronucleophiles with the acetylenic aldehyde TIPSC≡CCHO. Absolute stere
A divergent synthesis of triyne natural products and glycosylated analogues using a carbenoid rearrangement
Luu, Thanh,Shi, Wei,Lowary, Todd L.,Tykwinski, Rik R.
, p. 3167 - 3178 (2007/10/03)
Using a carbenoid rearrangement to introduce the conjugated acetylenic framework, a series of triynols has been synthesized in five steps from 1,4-butynediol. Several of the triyne alcohols are known natural products and others are glycosylated analogues.
Synthesis of Novel Fused β-Lactams by Intramolecular 1,3-Dipolar Cycloadditions. Part 9. Preparation of the 7-Oxo-1,3-dizabicycloheptane-2-carboxylate and 8-Oxo-1,3-dizabicyclooctane-2-carboxylate Ring Systems
Branch, Clive L.,Pearson, Michael J
, p. 1077 - 1096 (2007/10/02)
4-Vinylazetidin-2-one (24) has been converted into 1--4-vinylazetidin-2-one (27) and 1--4-(2-methoxycarbonylvinyl)-azetidin-2-one (43) which on thermolysis in toluene gave (2RS,5RS)-ben