insect sex attractants
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1980 ◽  
Vol 5 (4) ◽  
pp. 385-396 ◽  
Author(s):  
J. N. PERRY ◽  
C. WALL ◽  
A. R. GREENWAY


1979 ◽  
Vol 10 (35) ◽  
Author(s):  
P. I. SVIRSKAYA ◽  
C. C. LEZNOFF ◽  
J. WEATHERSTON ◽  
J. E. LAING


1979 ◽  
Vol 8 (4) ◽  
pp. 732-733 ◽  
Author(s):  
W. F. Steck ◽  
B. K. Bailey ◽  
M. D. Chisholm ◽  
E. W. Underhill


1979 ◽  
Vol 24 (2) ◽  
pp. 152-155 ◽  
Author(s):  
Polina I. Svirskaya ◽  
Clifford C. Leznoff ◽  
John Weatherston ◽  
John E. Laing


1978 ◽  
Vol 56 (7) ◽  
pp. 1031-1041 ◽  
Author(s):  
Thomas M. Fyles ◽  
Clifford C. Leznoff ◽  
John Weatherston

A 2% crosslinked divinylbenzene–styrene copolymer, incorporating benzoyl chloride groups, was used to monoprotect the symmetrical diol 1,10-decanediol. The corresponding monotrityl ether and cis-10-tetradecen-1-ol were prepared by this system, the latter by a Wittig reaction of a polymer-bound ylide with an aldehyde in the solution phase. A series of bifunctionalized resins containing proximally located trityl alcohol and benzoic acid groups was prepared in an attempt to prepare diol linked to the polymer via both a trityl ether and a benzoate linkage. It was established that these polymers bound 1,10-decanediol exclusively at one end only. Polymers, containing both trityl alcohol and benzoic acid groups in a random array or polymers containing proximally located trityl alcohol groups, gave mixtures of both monoprotected and doubly protected diol.



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