Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Matthew M. Salter"'
Lewis Acid-Mediated Acetal Substitution Reactions: Mechanism and Application to Asymmetric Catalysis
Autor:
Matthew M. Salter, Shu Kobayashi, Yi-Jing Chen, Kenzo Arai, Yasuhiro Yamashita, Takeshi Yamakawa
Publikováno v:
Advanced Synthesis & Catalysis. 353:1927-1932
Substitution reactions of acetals with carbon nucleophiles are fundamental and conventional organic reactions. We succeeded in the preparation of an optically active acetal, which reacted with a silyl enol ether smoothly to afford the desired adducts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a67a29d1f98e14940bb4ecae6961a938
https://doi.org/10.1002/adsc.201100346
https://doi.org/10.1002/adsc.201100346
Publikováno v:
Advanced Synthesis & Catalysis. 350:647-651
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83877c0e23b84787948c012f02f1a8ee
https://doi.org/10.1002/adsc.200700615
https://doi.org/10.1002/adsc.200700615
Publikováno v:
Tetrahedron. 62:3582-3599
The intramolecular cyclisation of tethered allyl bromides onto terminal alkynes mediated by metallic indium proceeds smoothly and cleanly in mixtures of THF and H2O to give unsaturated carbocycles and heterocycles in good yield. Alternatively, the cy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d734efd7fc85ef37f421e55f9c08f85b
https://doi.org/10.1016/j.tet.2006.01.094
https://doi.org/10.1016/j.tet.2006.01.094
Autor:
Nadia H. Bhatti, Matthew M. Salter
Publikováno v:
Tetrahedron Letters. 45:8379-8382
Treatment of tethered alkyne–allyl halides 1a–d with indium metal in halogenated solvents affords carbocyclic vinyl halides (3a–d ) via a novel atom-transfer reaction. The reactions are operationally facile and proceed smoothly at room temperat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71f0ecca9b4afb42f697dd6e1b4eff45
https://doi.org/10.1016/j.tetlet.2004.09.054
https://doi.org/10.1016/j.tetlet.2004.09.054
Publikováno v:
Chemistry - An Asian Journal. 5:493-495
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a366ca839e857971ddb6074f78bfc6e
https://doi.org/10.1002/asia.200900524
https://doi.org/10.1002/asia.200900524
Autor:
Matthew M. Salter, Kevin Flack, Jennifer C. Beall, Vernon C. Gibson, Braddock Dc, Anthony G. M. Barrett
Publikováno v:
The Journal of Organic Chemistry. 65:6508-6514
A novel strategy for the synthesis of D,L-glucosylceramide 1, a member of the glycosphingolipid class of natural products is described. Reagent-controlled asymmetric Brown allylboration gave excellent stereochemical control in the construction of adj
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ac4863d0937cf21208b1b5a4fbcd4c4
https://doi.org/10.1021/jo000690p
https://doi.org/10.1021/jo000690p
Autor:
D. Christopher Braddock, Panayiotis A. Procopiou, Jennifer C. Beall, Mahmood Ahmed, Vernon C. Gibson, Matthew M. Salter, Kevin Flack, Anthony G. M. Barrett
Publikováno v:
Tetrahedron. 55:3219-3232
Molybdenum carbene 6 catalyzed ring closing metathesis of (alkenyl)silyl ethers of homochiral allylic alcohols to afford 1,2-oxasilines which were elaborated in situ to give (E)-4-alkyl-1,2-disubstituted 3-buten-1-ol and (Z)-4-alkyl-4-silyl-1,2-disub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b0edacc61fce294834808cf371dae96
https://doi.org/10.1016/s0040-4020(98)01135-1
https://doi.org/10.1016/s0040-4020(98)01135-1
Publikováno v:
Angewandte Chemie International Edition. 46:955-957
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ecb3d948b8b781047c10f5460695085
https://doi.org/10.1002/anie.200603787
https://doi.org/10.1002/anie.200603787
Autor:
Matthew M. Salter, Takeshi Yamakawa, Kenzo Arai, Shu Kobayashi, Yasuhiro Yamashita, Yi-Jing Chen
Publikováno v:
ChemInform. 43
Substitution reactions of acetals with carbon nucleophiles are fundamental and conventional organic reactions. We succeeded in the preparation of an optically active acetal, which reacted with a silyl enol ether smoothly to afford the desired adducts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43e2385497b4db3ecd46e3b9d4a46c71
https://doi.org/10.1002/chin.201202029
https://doi.org/10.1002/chin.201202029
Publikováno v:
ChemInform. 42
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f61d0a50e0816ac0d15247bbb1a8410c
https://doi.org/10.1002/chin.201132235
https://doi.org/10.1002/chin.201132235