Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Matthew C. Walczak"'
Autor:
Robert S. Coleman, Matthew C. Walczak
Publikováno v:
The Journal of Organic Chemistry. 71:9841-9844
Convergent and efficient syntheses of the microbial natural products gymnoconjugatin A and B are reported and were based on a linchpin coupling strategy using a boron/tin hetero-bis-metallated butadiene system.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d97edcf09f69b814d5ea5793fb9e23bf
https://doi.org/10.1021/jo061755c
https://doi.org/10.1021/jo061755c
Autor:
Matthew C. Walczak, Paolo Pasetto
Publikováno v:
ChemInform. 41
C-Glycosides were successfully prepared via dehydrative alkylation under Mitsunobu conditions, using substituted sulfonyl methanes as nucleophiles. The materials prepared were converted to useful C-glycoside intermediates. An application of this appr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80a815b32d5988417811339f1ffcc62f
https://doi.org/10.1002/chin.201005196
https://doi.org/10.1002/chin.201005196
Autor:
Robert S. Coleman, Matthew C. Walczak
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[853335-17-8] C22H43BO2Sn (MW 469.10) InChI = 1S/C10H16BO2.3C4H9.Sn/c1-6-7-8-11-12-9(2,3)10(4,5)13-11;3*1-3-4-2;/h1,6-8H,2-5H3;3*1,3-4H2,2H3;/b6-1?,8-7+;;;; InChIKey = ZBEVVAJCXOEONR-XIZNWYPTSA-N (vinyl nucleophile in palladium-mediated cross-couplin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5234f4709899ee763b7d987b4a8785a
https://doi.org/10.1002/047084289x.rn00826
https://doi.org/10.1002/047084289x.rn00826
Autor:
Robert S. Coleman, Matthew C. Walczak
Publikováno v:
ChemInform. 38
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25f3f4e68b711dbf5845fc88bf1ea83d
https://doi.org/10.1002/chin.200720189
https://doi.org/10.1002/chin.200720189
Autor:
Robert S. Coleman, Matthew C. Walczak
Publikováno v:
ChemInform. 36
[structure: see text]. The synthesis of a hetero-bis-metallo 1,3-butadiene is reported, and its use as an orthogonal Stille and Suzuki-Miyaura coupling partner is detailed. The tin/boron diene participated successfully in a one-pot, sequential Stille
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f44eb06b5cff0d1a1ca48247ab4fae68
https://doi.org/10.1002/chin.200542108
https://doi.org/10.1002/chin.200542108
Publikováno v:
Journal of the American Chemical Society. 127:16038-16039
Hetero-bis-metalated 1,3-butadiene is employed in the lynchpin coupling of synthetic fragments of the side chain of the antitumor agent, lucilactaene. Sequential Stille and Suzuki−Miyaura couplings interpolate this unique boron/tin diene into the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c254a4a60cacbc0ee0804207532ed9d8
https://doi.org/10.1021/ja056217g
https://doi.org/10.1021/ja056217g
Publikováno v:
Synfacts. 2006:0418-0418
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::970a08215f0281cfe1f8e027a90920e0
https://doi.org/10.1055/s-2006-934396
https://doi.org/10.1055/s-2006-934396