ライフサイエンスコーパス: Stille coupling

1 size a chiral heterohelicene homodimer using Stille coupling.

2 be suitable for further functionalization by Stille coupling.

3 flates and vinyl chlorides to participate in Stille coupling.

4 y 20 kDa, in agreement with controls made by Stille coupling.

5 tannanes as intermediates and their use in a Stille coupling.

6 ine-substituted quinones can be exploited in Stille couplings.

7 ding a Wittig reaction, a Suzuki coupling, a Stille coupling, a Yamaguchi esterification and a Yamagu

8 e success was the use of a carefully defined Stille coupling and a Mukaiyama macrolactonization as we

9 ucleophilic additions, reductive aminations, Stille couplings, and polymer-assisted solution-phase (P

10 ing closing alkyne metathesis and a modified Stille coupling as the key transformations.

11 BODIPY that readily undergoes regioselective Stille coupling at the 8-position, or homo/mixed couplin

12 ompounds 11a,b were conveniently obtained by Stille coupling between 2,5-bis(tri-n-butylstannyl)furan

13 Stille coupling between these high E/Z 1-bromo-1-fluoroa

14 The final stages of the synthesis featured a Stille coupling between vinyl iodide 3 and vinylstannane

15 Utilizing CsF in POPd-catalyzed Stille couplings further increased the reactivity of ary

16 via Sn-Li exchange/electrophile trapping or Stille coupling generates a range of substituted bicycli

17 coupling of 2,4-dihalooxazoles followed by a Stille coupling has been successfully developed.

18 5,5'-dibromo-2,2'-bipyridine by consecutive Stille couplings is therefore illustrated and documented

19 ions of this reaction, an alternative to the Stille coupling, is summarized.

20 talyzed Negishi, Kumada, Suzuki, Hiyama, and Stille coupling methods showed that the latter affords h

21 lenes have been synthesized via Pd-catalyzed Stille coupling of 1,8-dibromonaphthalene and 2-alkyl-4-

22 -5'-n-hexyl-2,2'-bipyridine were obtained by Stille coupling of 2,5-dibromopyridine with 2-trimethyls

23 A1 was accomplished using as the key step a Stille coupling of a 2,5-dibromobenzoquinone with an (N-

24 f a novel bifunctional oxazole linchpin; and Stille coupling of a C(28) trimethyl stannane with a C(2

25 ditional E,E 1,3-diene, was achieved through Stille coupling of an acetylene-derived vinyl stannane a

26 This synthesis proceeds via the Stille coupling of appropriately functionalized pyridine

27 Stille coupling of the glycosidated aglycon 128 with die

28 Stille coupling of the resulting pure quasienantiomers w

29 ed by either Suzuki-Miyaura, Sonogashira, or Stille couplings of the corresponding A- and C,D-ring fr

30 olymers, in a single reaction step employing Stille coupling polymerization of end-functional polythi

31 ed using BDTT, BDTP, FDPP, and DPP units via Stille-coupling polymerization.

32 ne-pot tandem Pd-catalyzed hydrostannylation/Stille coupling protocol for the stereoselective generat

33 units (DTP-co-THs) were synthesized using a Stille coupling reaction and exhibited molecular weights

34 eaction to construct the C(20)-C(21) bond, a Stille coupling reaction to form the C(11)-C(12) bond, a

35 clization technology in combination with the Stille coupling reaction.

36 is(dicarboximide)s have been synthesized via Stille coupling reactions of the corresponding 2,6-dista

37 We first utilized Suzuki and Stille coupling reactions through protection and deprote

38 sequential Sonogashira/Suzuki or Sonagashira/Stille coupling reactions.

39 10 (R = SnMe(3)), which we have applied for Stille coupling reactions.

40 aphthol, have been synthesized by Suzuki and Stille coupling reactions.

41 iazoles by the Pd-catalyzed Sonogashira, and Stille coupling reactions.

42 ne 13 and its subsequent palladium-catalyzed Stille coupling to 61b.

43 sformation were successfully derivatized via Stille coupling to a variety of trisubstituted alkene pr

44 ruct the 13-membered ring, an intramolecular Stille coupling to fashion the unsaturated 14-membered m

45 cyclization to construct the helicene, and a Stille coupling to incorporate the DMAP unit.

46 Stille coupling under standard carbonylative conditions

47 porphyrin undergo facile palladium-catalyzed Stille coupling with 3-isopropoxy-2-tri-n-butylstannyl-c

48 -bromovinylporphyrin, which underwent facile Stille coupling with 3-isopropoxy-2-tri-n-butylstannylcy

49 verted to trans-vinylstannane 47 which, in a Stille coupling with allylic chloride 50, gave 51.

50 combination of the Bartoli reaction and the Stille coupling with an appropriate pyridyl stannane.