A new synthesis of (Z,E)-tetradec-11-enyl acetate, the sex attractant of the omnivorous leafroller (Archips podana)

1996 ◽  
Vol 45 (8) ◽  
pp. 2022-2024 ◽  
Author(s):  
V. I. Bykov ◽  
L. V. Kelbakiani ◽  
T. A. Butenko ◽  
E. Sh. Finkel'shtein

ChemInform ◽  
2010 ◽  
Vol 28 (9) ◽  
pp. no-no
Author(s):  
V. I. BYKOV ◽  
L. V. KELBAKIANI ◽  
T. A. BUTENKO ◽  
E. SH. FINKEL'SHTEIN


1973 ◽  
Vol 9 (4) ◽  
pp. 509-511
Author(s):  
A. A. Shamshurin ◽  
M. A. Rekhter ◽  
L. A. Vlad


1996 ◽  
Vol 61 (26) ◽  
pp. 9635-9635
Author(s):  
Alicia Boto ◽  
Rosendo Hernández ◽  
Ernesto Suárez ◽  
Carmen Betancor ◽  
María S. Rodríguez


Synlett ◽  
1991 ◽  
Vol 1991 (04) ◽  
pp. 356-358 ◽  
Author(s):  
Bernd Burkhart ◽  
Steffen Krill ◽  
Yoshinori Okano ◽  
Wataru Ando ◽  
Manfred Regitz
Keyword(s):  


2016 ◽  
Vol 31 (5) ◽  
pp. 523
Author(s):  
MA Hong-Bing ◽  
BAI Hua ◽  
XUE Chen ◽  
TAO Peng-Fei ◽  
XU Qun-Feng ◽  
...  
Keyword(s):  




2015 ◽  
Vol 19 (13) ◽  
pp. 1292-1300 ◽  
Author(s):  
Amelia Diaz ◽  
J. Manuel Lopez–Romero ◽  
Rafael Contreras-Caceres ◽  
Manuel Algarra ◽  
Rodrigo Rico ◽  
...  


2019 ◽  
Vol 16 (12) ◽  
pp. 931-934 ◽  
Author(s):  
Alexandra Kamlah ◽  
Franz Bracher

: A new synthesis of the 2,6-naphthyridine alkaloid 4-methyl-2,6-naphthyridine from Antirrhinum majus has been developed. Key steps are a regioselective oxidation of 3-bromo-4,5- dimethylpyridine to the corresponding 4-formyl derivative, and the annulation of the second pyridine ring by Suzuki-Miyaura cross-coupling using (E)-2-ethoxyvinylboronic acid pinacol ester as a masked acetaldehyde equivalent. This protocol gives the alkaloid in four steps starting from commercially available 3,4-dimethylpyridine in 15% overall yield. This annulation protocol should be useful for the synthesis of other condensed pyridines as well.



Sign in / Sign up

Export Citation Format

Share Document