| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A new irreversible inhibitor of soybean lipoxygenase; relevance to mechanism
|
Corey, E.J.
|
|
1986
|
27 |
31 |
p. 3585-3588
4 p.
|
artikel
|
| 2 |
A versatile reagent for synthesis of α-hydroxy aldehydes and ketones —methylthiomethyl p-tolyl sulfone
|
Ogura, Katsuyuki
|
|
1986
|
27 |
31 |
p. 3665-3668
4 p.
|
artikel
|
| 3 |
Carbocation NMR isotope shifts analogous to inverse γ-deuterium isotope effects
|
Forsyth, David A.
|
|
1986
|
27 |
31 |
p. 3569-3572
4 p.
|
artikel
|
| 4 |
Co(II)porphyrin catalyzed isomerization of bicyclobutanecarbonitrile
|
Miki, Sadao
|
|
1986
|
27 |
31 |
p. 3669-3672
4 p.
|
artikel
|
| 5 |
Copper catalysed O -phenylation of phenols and enols by pentavalent organobismuth compounds
|
Barton, Derek H.R
|
|
1986
|
27 |
31 |
p. 3619-3622
4 p.
|
artikel
|
| 6 |
C(2)-stereocontrol of δ-lactones via acid-catalyzed cyclization of ketene dithioacetal having an internal hydroxyl group
|
Suzuki, Keisuke
|
|
1986
|
27 |
31 |
p. 3661-3664
4 p.
|
artikel
|
| 7 |
β-deuterium kinetic isotope effects in the solvolysis of 2-aryl-1,1,1-trifluoro-2-propyl tosylates and of 2-aryl-2-profyl p -nitrobenzoates. Evidence for a variation of the contribution of α-methyl substituent in stabilizing cationic reaction centers with different electron demand
|
Liu, Kwang-Ting
|
|
1986
|
27 |
31 |
p. 3623-3626
4 p.
|
artikel
|
| 8 |
Diastereoselective synthesis of 2,3,4-trisubstituted γ-lactols and γ-lactones via regio- and stereocontrolled opening of a 1,2-epoxy-4-hydroxyalkyl carbamate with hetero-nucleophiles
|
Lüßmann, Jörg
|
|
1986
|
27 |
31 |
p. 3595-3598
4 p.
|
artikel
|
| 9 |
Erratum
|
|
|
1986
|
27 |
31 |
p. 3556-
1 p.
|
artikel
|
| 10 |
Erster nachweis eines cyclopropenylcarbinyl-kations
|
Maier, Günther
|
|
1986
|
27 |
31 |
p. 3607-3610
4 p.
|
artikel
|
| 11 |
Formation and reaction of N-substituted peroxycarboximidic acids from α-azobenzyl hydroperoxides by pyridine-catalyzed reaction
|
Tezuka, Takahiro
|
|
1986
|
27 |
31 |
p. 3627-3630
4 p.
|
artikel
|
| 12 |
Graphical abstracts
|
|
|
1986
|
27 |
31 |
p. 3557-3563
7 p.
|
artikel
|
| 13 |
Highly diastereoselective synthesis of 1,2-epoxy-4-hydroxyalkyl carbamates. Masked and activated α,γ-dihydroxy-alkanals and -alkanones
|
Hoppe, Dieter
|
|
1986
|
27 |
31 |
p. 3591-3594
4 p.
|
artikel
|
| 14 |
Highly regio- and stereocontrolled halogenation of 1,1-difluoro-2-halo-1-alken-3-ols as applied to polyfluorinated pyrethroid synthesis
|
Fujita, Makoto
|
|
1986
|
27 |
31 |
p. 3659-3660
2 p.
|
artikel
|
| 15 |
Highly stereoselective synthesis of methynolide, the aglycone of the 12-membered ring macrolide methymycin, from D-glucose
|
Oikawa, Yuji
|
|
1986
|
27 |
31 |
p. 3647-3650
4 p.
|
artikel
|
| 16 |
Lewis acid catalyzed rearrangements of structurally related α,β-unsaturated epoxy ketones and oximes. A complementary approach to the synthesis of isomeric 1,4-diketospiro[n,m] alkanes.
|
Bach, Robert D.
|
|
1986
|
27 |
31 |
p. 3565-3568
4 p.
|
artikel
|
| 17 |
Metallic copper catalysis of N -arylation of amines by triarylbismuth diacylates
|
Barton, Derek H.R
|
|
1986
|
27 |
31 |
p. 3615-3618
4 p.
|
artikel
|
| 18 |
12-methylidene-10(Z), 13(Z)-nonadecadienoic acid, a new irreversible inhibitor of soybean lipoxygenase
|
Corey, E.J.
|
|
1986
|
27 |
31 |
p. 3589-3590
2 p.
|
artikel
|
| 19 |
Practical ways from aldehydes to 2-chloro-1,1,1-trifluoro-2-alkenes and 2-chloro-1,1-difluoro-1-alken-3-ols
|
Fujita, Makoto
|
|
1986
|
27 |
31 |
p. 3655-3658
4 p.
|
artikel
|
| 20 |
Promising cyclization reactions to construct the ring systems of brevianamides A,B
|
Williams, Robert M
|
|
1986
|
27 |
31 |
p. 3581-3584
4 p.
|
artikel
|
| 21 |
Simple synthesis and separation of the diastereomers of α-thio analogs of ribo- and deoxyribo- di- and triphosphates
|
Goody, R.S.
|
|
1986
|
27 |
31 |
p. 3599-3602
4 p.
|
artikel
|
| 22 |
Stereoselective addition of lithioethyl acetate to Boc-l-prolinal. A convenient chiral synthetic building block for the pyrrolizidine alkaloid ring system
|
Hanson, Gunnar J.
|
|
1986
|
27 |
31 |
p. 3577-3580
4 p.
|
artikel
|
| 23 |
Stereospecific rhodium(I) catalyzed desulfurization of thiiranes
|
Calet, Serge
|
|
1986
|
27 |
31 |
p. 3573-3576
4 p.
|
artikel
|
| 24 |
Synthesis and rearrangement of functionalized dispiro[2.1.3.3]Undecanes - preferred C4C5 over C3C4 ring enlargements
|
Fitjer, Lutz
|
|
1986
|
27 |
31 |
p. 3603-3606
4 p.
|
artikel
|
| 25 |
Synthesis of the pheromone of the comstock mealybug via a sila-cope elimination
|
Fall, Yagamare
|
|
1986
|
27 |
31 |
p. 3611-3614
4 p.
|
artikel
|
| 26 |
Synthetic study towards man-designed bleomycins. Synthesis of a DNA cleaving molecule based on bleomycin.
|
Otsuka, Masami
|
|
1986
|
27 |
31 |
p. 3639-3642
4 p.
|
artikel
|
| 27 |
Tandem [2,3]sigmatropic rearrangement of a sulphonium ylide and cyclopropanation of the resulting electron-rich olefin on a 4-methoxy-2-pyrone derivative
|
de March, P.
|
|
1986
|
27 |
31 |
p. 3673-3674
2 p.
|
artikel
|
| 28 |
Total synthesis and the absolute configuration of aurovertin B
|
Nishiyama, Shigeru
|
|
1986
|
27 |
31 |
p. 3643-3646
4 p.
|
artikel
|
| 29 |
Total synthesis of tylonolide, the aglycone of the 16-membered ring macrolide tylosin, from D-glucose. Selective application of MPM and DMPM protecting groups for hydroxy functions
|
Tanaka, Tatsuyoshi
|
|
1986
|
27 |
31 |
p. 3651-3654
4 p.
|
artikel
|
| 30 |
Transition-metal binding site of bleomycin. A remarkably efficient dioxygen-activating molecule based on bleomycin-Fe(II) complex
|
Kittaka, Atsushi
|
|
1986
|
27 |
31 |
p. 3631-3634
4 p.
|
artikel
|
| 31 |
Transition-metal binding site of bleomycin. A synthetic analogue equivalent to bleomycin in activating molecular oxygen
|
Sugano, Yuichi
|
|
1986
|
27 |
31 |
p. 3635-3638
4 p.
|
artikel
|
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