79827-34-2Relevant academic research and scientific papers
Volatiles from the ascomycete: Daldinia cf. childiae (Hypoxylaceae), originating from China
Lauterbach, Lukas,Wang, Tao,Stadler, Marc,Dickschat, Jeroen S.
, p. 726 - 734 (2019)
The volatiles from an isolate of the fungus Daldinia cf. childiae, obtained from a specimen collected in China, were collected by use of a closed-loop stripping apparatus and analysed by GC-MS. A total number of 33 compounds from different classes were ri
A stereoselective synthesis of nonracemic (+)-desoxoprosophylline by a tandem Wittig [2+3]-cycloaddition reaction
Herdeis, Claus,Telser, Joachim
, p. 1407 - 1414 (1999)
L-Ascorbic acid serves as chiral starting material for the synthesis of (+)-desoxoprosophylline. The synthetic pathway includes the formation of an O-protected 5-azido-2,3-dideoxysugar which is subjected to a tandem Wittig [2+3] cycloaddition reaction, le
Synthesis and characterization of hexadecadienyl compounds with a conjugated diene system, sex pheromone of the persimmon fruit moth and related compounds
Nishida, Takanobu,Vang, Le Van,Yamazawa, Hiroyuki,Yoshida, Ryuji,Naka, Hideshi,Tsuchida, Koji,Ando, Tetsu
, p. 822 - 829 (2007/10/03)
Hexadecadien-1-ol and the derivatives (acetate and aldehyde) with a conjugated diene system have recently been identified from a pheromone gland extract of the persimmon fruit moth (Stathmopoda masinissa), a pest insect of persimmon fruits distributed in
1,4- and 1,5-Stereoselection by Sequential Aldol Addition to α,β-Unsaturated Aldehydes Followed by Claisen Rearrangement. Application to Total Synthesis of the Vitamin E Side Chain and the Archaebacterial C40 Diol
Heathcock, Clayton H.,Finkelstein, Bruce L.,Jarvi, Esa T.,Radel, Peggy A.,Hadley, Cheri H.
, p. 1922 - 1942 (2007/10/02)
A synthetic strategy has been developed wherein the high 1,2-stereoselection obtainable from aldol reaction of an α,β-unsaturated aldehyde is parlayed by a subsequent Claisen rearrangement into 1,4- or 1,5-stereoselection.For example, diol monoethers 26 a
