ライフサイエンスコーパス: ring-opening polymerization

1 rying initiation sites by the living anionic ring opening polymerization.

2 avable linker is achieved by organocatalyzed ring-opening polymerization.

3 thioureas that catalyses rapid and selective ring-opening polymerizations.

4 ) as the matrix phase using a combination of ring-opening polymerizations.

5 nation of metal-free organo-catalytic living ring-opening polymerization and post-polymerization chai

6 some of the unique features of zwitterionic ring-opening polymerization and provides a useful mechan

7 ation (rROP) combines the advantages of both ring-opening polymerization and radical polymerization,

8 acetylene groups were prepared by controlled ring-opening polymerization and subsequently used for gr

9 - or DL-propargylglycine were synthesized by ring-opening polymerization and thiol-ene/yne photochemi

10 Mw/Mn = 1.05-1.17) were obtained via anionic ring opening polymerization (AROP) with molecular weight

11 The thermodynamics of the ring-opening polymerization depends sensitively on the h

12 zed by an ultrafast (<5 min) organocatalyzed ring-opening polymerization in a two-step, one-pot manne

13 An organocatalyzed ring-opening polymerization methodology was developed fo

14 ,4,5-tetramethyl-imidazol-2-ylidene (4), the ring-opening polymerization occurs within minutes at roo

15 degradable polymer prepared by the catalyzed ring opening polymerization of lactide.

16 that employs relay metathesis to promote the ring opening polymerization of unstrained macrocyclic st

17 Attempts to induce thermal or anionic ring-opening polymerization of 4a-c were unsuccessful an

18 dispersity are synthesized using an anionic ring-opening polymerization of a beta-lactam sugar monom

19 The ring-opening polymerization of a mixture of enantiomeric

20 eport the synthesis, reactivity studies, and ring-opening polymerization of a tricarba[3]nickelocenop

21 hylsilyl (N-TMS) amine to mediate controlled ring-opening polymerization of amino acid N-carboxyanhyd

22 mide linkages are synthesized by the anionic ring-opening polymerization of an altrose beta-lactam mo

23 ck length ratios were obtained by sequential ring-opening polymerization of benzyl-L-glutamate and pr

24 mbers of the nylon-3 family, are prepared by ring-opening polymerization of beta-lactams.

25 lar weight cyclic polyketals by the cationic ring-opening polymerization of bicyclic ketal monomers,

26 erein we report an expedient organocatalytic ring-opening polymerization of cyclic carbonates contain

27 he polymerization of olefins and dienes, the ring-opening polymerization of cyclic esters or the guan

28 ysis, depolymerization of branched polymers, ring-opening polymerization of cycloalkanes, and other u

29 y, the benzoin condensation reaction and the ring-opening polymerization of d,l-lactide, respectively

30 The ring-opening polymerization of epsilon-caprolactone can

31 as macroinitiator for the aluminum-mediated ring-opening polymerization of epsilon-caprolactone to p

32 d on the use of dendritic initiators for the ring-opening polymerization of epsilon-caprolactone to y

33 e and ethylene carbonate, was synthesized by ring-opening polymerization of ethylene carbonate.

34 es synthesized by metal-free organocatalytic ring-opening polymerization of functional cyclic carbona

35 Ring-opening polymerization of functional monomers has e

36 Glycopolypeptides (GPs) were synthesized by ring-opening polymerization of glycosylated N-carboxyanh

37 s controlled using redox reagents during the ring-opening polymerization of l-lactide and epsilon-cap

38 The ring-opening polymerization of L-lactide mediated by the

39 estigated two alternative mechanisms for the ring-opening polymerization of l-lactide using a guanidi

40 s controlled using redox reagents during the ring-opening polymerization of L-lactide.

41 ) NPs (termed CsA-NPs) through CsA-initiated ring-opening polymerization of lactide (LA) followed by

42 amine or a phosphine) promote the controlled ring-opening polymerization of lactide and epsilon-capro

43 ionic liquid, and was found to catalyze the ring-opening polymerization of lactide at elevated tempe

44 The zwitterionic ring-opening polymerization of lactide initiated by N-he

45 as macroinitiators to subsequently initiate ring-opening polymerization of lactide to synthesize the

46 single-component catalyst/initiators for the ring-opening polymerization of lactide under mild condit

47 styrene oxide SO/CO(2) copolymerization and ring-opening polymerization of lactide with DBU (1,8-dia

48 produced commercially by the metal-catalyzed ring-opening polymerization of lactide.

49 d to prepare block copolyesters by combining ring-opening polymerization of lactones and ring-opening

50 Ring-opening polymerization of lactones is a versatile a

51 The organocatalytic ring-opening polymerization of N-acyl morpholin-2-ones o

52 Synthetic polypeptides from the ring-opening polymerization of N-carboxyanhydrides (NCAs

53 cyclooctynol (DIBO) was used to initiate the ring-opening polymerization of poly(gamma-benzyl-L-gluta

54 phasalen initiators for the stereocontrolled ring-opening polymerization of rac-lactide are reported.

55 ltaneously fast and selective for the living ring-opening polymerization of several common monomers,

56 ough synthetic cascades of ROAMP followed by ring-opening polymerization of strained epsilon-caprolac

57 opening metathesis polymerization (ROMP) and ring-opening polymerization of the amino acid N-carboxya

58 Controllable ring-opening polymerization of the heteroleptic tin-brid

59 The thermodynamics and kinetics of ring-opening polymerization of the two dithiolanes were

60 copolymer was synthesized by initiating the ring-opening polymerization of trimethylene carbonate (T

61 wo processes, namely 101.9 kJ x mol (-1) for ring-opening polymerization of trimethylene carbonate an

62 addition of a thiol initiates the reversible ring-opening polymerizations of dithiolanes in the micel

63 e of oligomer length, by the organocatalytic ring-opening polymerization (OROP) of 5-membered cyclic

64 hilic polyoxazoline chain is grafted through ring opening polymerization, possess homogeneous spheric

65 Organocatalytic ring opening polymerization (ROP) of eight-membered cycl

66 Ring-opening polymerization (ROP) is a powerful syntheti

67 Ring-opening polymerization (ROP) of an allyl-substitute

68 zation can be regulated and switched between ring-opening polymerization (ROP) of BBL and CHO/CO2 cop

69 methods for accessing these materials is the ring-opening polymerization (ROP) of cyclic monomers.

70 family were highly active catalysts for the ring-opening polymerization (ROP) of lactide (LA) to for

71 Here a single switchable catalyst for both ring-opening polymerization (ROP) of lactones and ring-o

72 ntional chemoselectivity to enable the first ring-opening polymerization (ROP) of MBL, thereby produc

73 N-Heterocyclic carbene (NHC)-mediated ring-opening polymerization (ROP) of N-substituted N-car

74 catalyst to a polymer in the organocatalyzed ring-opening polymerization (ROP) of rac-lactide (rac-LA

75 Iso-selective initiators for the ring-opening polymerization (ROP) of rac-lactide are rar

76 d adduct (PyMA) as an organocatalyst for the ring-opening polymerization (ROP) of the cyclic O-carbox

77 carbenes were found to be more active toward ring-opening polymerization (ROP) than their sterically

78 design of complex single-site catalysts for ring-opening polymerization (ROP) to enhance both activi

79 a class of viable monomers which can undergo ring-opening polymerization (ROP) to prepare poly(alpha-

80 oup in their side chain that readily undergo ring-opening polymerization (ROP).

81 Radical ring-opening polymerization (rROP) combines the advantag

82 Our six-membered cyclic phosphoester ring-opening polymerization strategy is demonstrated, he

83 is achieved via a regio- and stereoselective ring opening polymerization to generate multiple glycosi

84 he strained 3',5'-cyclic monomer can promote ring-opening polymerization to afford the resulting poly

85 hexane (50%), while 2a, 2b, and 3a underwent ring-opening polymerization under the reaction condition