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1 ced in a single step via a late-stage double Stille coupling.
2 tannanes as intermediates and their use in a Stille coupling.
3 size a chiral heterohelicene homodimer using Stille coupling.
4 be suitable for further functionalization by Stille coupling.
5 flates and vinyl chlorides to participate in Stille coupling.
6 e-thiophene co-oligomer type spirodimers via Stille coupling.
7 allation of a vinyl methoxy ether moiety via Stille coupling.
8 lymer synthesized through thermal-activation Stille coupling.
9 y 20 kDa, in agreement with controls made by Stille coupling.
10 ine-substituted quinones can be exploited in Stille couplings.
11 ding a Wittig reaction, a Suzuki coupling, a Stille coupling, a Yamaguchi esterification and a Yamagu
12 e success was the use of a carefully defined Stille coupling and a Mukaiyama macrolactonization as we
13 onsecutive chain extension steps involving a Stille coupling and a stereospecific olefin cross-metath
14                                 A convergent Stille coupling and phenol-directed hydrogenation united
15 ucleophilic additions, reductive aminations, Stille couplings, and polymer-assisted solution-phase (P
16 ing closing alkyne metathesis and a modified Stille coupling as the key transformations.
17 BODIPY that readily undergoes regioselective Stille coupling at the 8-position, or homo/mixed couplin
18 ompounds 11a,b were conveniently obtained by Stille coupling between 2,5-bis(tri-n-butylstannyl)furan
19                                              Stille coupling between these high E/Z 1-bromo-1-fluoroa
20 The final stages of the synthesis featured a Stille coupling between vinyl iodide 3 and vinylstannane
21 orodienes by an unprecedented site-selective Stille coupling followed by copper-mediated tin/chlorine
22              Utilizing CsF in POPd-catalyzed Stille couplings further increased the reactivity of ary
23  via Sn-Li exchange/electrophile trapping or Stille coupling generates a range of substituted bicycli
24 coupling of 2,4-dihalooxazoles followed by a Stille coupling has been successfully developed.
25  5,5'-dibromo-2,2'-bipyridine by consecutive Stille couplings is therefore illustrated and documented
26 ions of this reaction, an alternative to the Stille coupling, is summarized.
27 talyzed Negishi, Kumada, Suzuki, Hiyama, and Stille coupling methods showed that the latter affords h
28 lenes have been synthesized via Pd-catalyzed Stille coupling of 1,8-dibromonaphthalene and 2-alkyl-4-
29 -5'-n-hexyl-2,2'-bipyridine were obtained by Stille coupling of 2,5-dibromopyridine with 2-trimethyls
30  A1 was accomplished using as the key step a Stille coupling of a 2,5-dibromobenzoquinone with an (N-
31 f a novel bifunctional oxazole linchpin; and Stille coupling of a C(28) trimethyl stannane with a C(2
32 ditional E,E 1,3-diene, was achieved through Stille coupling of an acetylene-derived vinyl stannane a
33              This synthesis proceeds via the Stille coupling of appropriately functionalized pyridine
34                                              Stille coupling of the glycosidated aglycon 128 with die
35                                              Stille coupling of the resulting pure quasienantiomers w
36 ed by either Suzuki-Miyaura, Sonogashira, or Stille couplings of the corresponding A- and C,D-ring fr
37 olymers, in a single reaction step employing Stille coupling polymerization of end-functional polythi
38 ed using BDTT, BDTP, FDPP, and DPP units via Stille-coupling polymerization.
39 ne-pot tandem Pd-catalyzed hydrostannylation/Stille coupling protocol for the stereoselective generat
40  units (DTP-co-THs) were synthesized using a Stille coupling reaction and exhibited molecular weights
41 eaction to construct the C(20)-C(21) bond, a Stille coupling reaction to form the C(11)-C(12) bond, a
42 clization technology in combination with the Stille coupling reaction.
43 is(dicarboximide)s have been synthesized via Stille coupling reactions of the corresponding 2,6-dista
44                 We first utilized Suzuki and Stille coupling reactions through protection and deprote
45 iazoles by the Pd-catalyzed Sonogashira, and Stille coupling reactions.
46  10 (R = SnMe(3)), which we have applied for Stille coupling reactions.
47 sequential Sonogashira/Suzuki or Sonagashira/Stille coupling reactions.
48 aphthol, have been synthesized by Suzuki and Stille coupling reactions.
49 ne 13 and its subsequent palladium-catalyzed Stille coupling to 61b.
50 sformation were successfully derivatized via Stille coupling to a variety of trisubstituted alkene pr
51 ruct the 13-membered ring, an intramolecular Stille coupling to fashion the unsaturated 14-membered m
52 am and macrocycle fragments were united by a Stille coupling to furnish sanglifehrin A and B.
53 cyclization to construct the helicene, and a Stille coupling to incorporate the DMAP unit.
54                                              Stille coupling under standard carbonylative conditions
55 porphyrin undergo facile palladium-catalyzed Stille coupling with 3-isopropoxy-2-tri-n-butylstannyl-c
56 -bromovinylporphyrin, which underwent facile Stille coupling with 3-isopropoxy-2-tri-n-butylstannylcy
57 verted to trans-vinylstannane 47 which, in a Stille coupling with allylic chloride 50, gave 51.
58  combination of the Bartoli reaction and the Stille coupling with an appropriate pyridyl stannane.