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Page 1: kanai/seminar/pdf/Lit_Furutachi_M2.pdfMeO MeO a Aspidophytine Construction of fragment 1 CHO N02 OMe OMe N 1-12 MeO 0Me Me fragment 1 CHO OHC OlPr TMS fragment 2 OH OTBS TMS Cc,nstruction
Page 2: kanai/seminar/pdf/Lit_Furutachi_M2.pdfMeO MeO a Aspidophytine Construction of fragment 1 CHO N02 OMe OMe N 1-12 MeO 0Me Me fragment 1 CHO OHC OlPr TMS fragment 2 OH OTBS TMS Cc,nstruction
Page 3: kanai/seminar/pdf/Lit_Furutachi_M2.pdfMeO MeO a Aspidophytine Construction of fragment 1 CHO N02 OMe OMe N 1-12 MeO 0Me Me fragment 1 CHO OHC OlPr TMS fragment 2 OH OTBS TMS Cc,nstruction
Page 4: kanai/seminar/pdf/Lit_Furutachi_M2.pdfMeO MeO a Aspidophytine Construction of fragment 1 CHO N02 OMe OMe N 1-12 MeO 0Me Me fragment 1 CHO OHC OlPr TMS fragment 2 OH OTBS TMS Cc,nstruction
Page 5: kanai/seminar/pdf/Lit_Furutachi_M2.pdfMeO MeO a Aspidophytine Construction of fragment 1 CHO N02 OMe OMe N 1-12 MeO 0Me Me fragment 1 CHO OHC OlPr TMS fragment 2 OH OTBS TMS Cc,nstruction
Page 6: kanai/seminar/pdf/Lit_Furutachi_M2.pdfMeO MeO a Aspidophytine Construction of fragment 1 CHO N02 OMe OMe N 1-12 MeO 0Me Me fragment 1 CHO OHC OlPr TMS fragment 2 OH OTBS TMS Cc,nstruction
Page 7: kanai/seminar/pdf/Lit_Furutachi_M2.pdfMeO MeO a Aspidophytine Construction of fragment 1 CHO N02 OMe OMe N 1-12 MeO 0Me Me fragment 1 CHO OHC OlPr TMS fragment 2 OH OTBS TMS Cc,nstruction
Page 8: kanai/seminar/pdf/Lit_Furutachi_M2.pdfMeO MeO a Aspidophytine Construction of fragment 1 CHO N02 OMe OMe N 1-12 MeO 0Me Me fragment 1 CHO OHC OlPr TMS fragment 2 OH OTBS TMS Cc,nstruction
Page 9: kanai/seminar/pdf/Lit_Furutachi_M2.pdfMeO MeO a Aspidophytine Construction of fragment 1 CHO N02 OMe OMe N 1-12 MeO 0Me Me fragment 1 CHO OHC OlPr TMS fragment 2 OH OTBS TMS Cc,nstruction
Page 10: kanai/seminar/pdf/Lit_Furutachi_M2.pdfMeO MeO a Aspidophytine Construction of fragment 1 CHO N02 OMe OMe N 1-12 MeO 0Me Me fragment 1 CHO OHC OlPr TMS fragment 2 OH OTBS TMS Cc,nstruction
Page 11: kanai/seminar/pdf/Lit_Furutachi_M2.pdfMeO MeO a Aspidophytine Construction of fragment 1 CHO N02 OMe OMe N 1-12 MeO 0Me Me fragment 1 CHO OHC OlPr TMS fragment 2 OH OTBS TMS Cc,nstruction
Page 12: kanai/seminar/pdf/Lit_Furutachi_M2.pdfMeO MeO a Aspidophytine Construction of fragment 1 CHO N02 OMe OMe N 1-12 MeO 0Me Me fragment 1 CHO OHC OlPr TMS fragment 2 OH OTBS TMS Cc,nstruction
Page 13: kanai/seminar/pdf/Lit_Furutachi_M2.pdfMeO MeO a Aspidophytine Construction of fragment 1 CHO N02 OMe OMe N 1-12 MeO 0Me Me fragment 1 CHO OHC OlPr TMS fragment 2 OH OTBS TMS Cc,nstruction
Page 14: kanai/seminar/pdf/Lit_Furutachi_M2.pdfMeO MeO a Aspidophytine Construction of fragment 1 CHO N02 OMe OMe N 1-12 MeO 0Me Me fragment 1 CHO OHC OlPr TMS fragment 2 OH OTBS TMS Cc,nstruction
Page 15: kanai/seminar/pdf/Lit_Furutachi_M2.pdfMeO MeO a Aspidophytine Construction of fragment 1 CHO N02 OMe OMe N 1-12 MeO 0Me Me fragment 1 CHO OHC OlPr TMS fragment 2 OH OTBS TMS Cc,nstruction
Page 16: kanai/seminar/pdf/Lit_Furutachi_M2.pdfMeO MeO a Aspidophytine Construction of fragment 1 CHO N02 OMe OMe N 1-12 MeO 0Me Me fragment 1 CHO OHC OlPr TMS fragment 2 OH OTBS TMS Cc,nstruction

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TotalSynthesisandStructuralRevisionof ...ccc.chem.pitt.edu/wipf/Current Literature/Jared_7.pdfCylcobutaneCHArylaon I OMe MeO MeO (2 equiv) Pd(OAc)2 (15 mol%), Ag2CO3 (1.5 equiv), PivOH

| OME-ftp.icpdas.com.tw/pub/beta_version/Omega_RemoteIO/OME-ET-7000… · OME-ET-7026/OME-PET-7026.....37 OME-ET-7042/OME-PET-7042 ... each AI channel must correspond to the input

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Reagents for Alkylidenations - Home | Princeton Universityorggroup/supergroup_pdf... · Reetz ( Ti ), Tani ( Zn/V ... S.J. et. al. J. Org. Chem. 1988, 53 ... DDQ, THF O MeO Me O OMe

20150516 MeO OMegousei/synthetic/mondai/zemi-toi/zemitoi… · 20150516 MeO OMe Cl Cl Cl Cl Me H H 1) OsO4, NMO acetone/H2O, rt, 90% 2) BF3·OEt2, toluene reflux, 46% Me Cl O Cl Cl

X ativante + Nu + ativante X - Nu Mecanismo: A) Uma etapa com estado de transição Cl NO 2 2 + MeO - Cl OMe NO 2 2 2 2 OMe + Cl - Ou B) Duas etapas com

熊谷英彦名誉教授「平成24年度日本学士院賞」受賞 ...NMe HO MeO OH OH H NMe HO MeO OMe OH H N OH OMe MeO HO H 3 12 / 25 7月21日（土）、「いしかわ食の再発見」をテーマに石川県立大学公

SCH 511 - University of Nairobi Personal Websites · PDF fileSCH 511 Dr. Solomon Derese 107 ... basically the same except that the β-keto group is ... MeO OMe H OH MeO MeO O O O MeO

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Tema 4. Heterociclos - ocw.ehu.eus · MeO MeO OMe O Cl MeO MeO OMe O N O H N O base trimetozina (tranquilizante y relajante muscular) N Me H N Ph Ph Cl SN1 Ph Ph NNMe ciclizina (travel-sickness

Utilisation of Extractives - Åbo Akademiweb.abo.fi/instut/pcc/presentations_pdf/Holmbom... · 2010. 4. 23. · Knots: the richest source of polyphenols in nature. MeO HO OH OMe OH

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Almost-Impossible Materials Science by 3D Diffraction Microscopy · 2007. 8. 20. · CH 3 O R OH X Y + Si MeO OMe OMe O O + Al(OsBu) 3 Materials Science and Engineering ... P. Evans

DOI: 10.1595/147106709X474226 Novel Chiral Chemistries ... · PDF fileNovel Chiral Chemistries Japan 2009 ... MeO MeO OMe PAr2 PAr2 3 ... well as retaining its selectivity with β-keto

CHAPTER 3 - CaltechTHESISthesis.library.caltech.edu/5986/4/Ch3_final.pdf212 Cl phenol 208 ca.CSA PhH,85 N H NCO2Me 213 OH OMe MeO 3 2 O OMe OMe 209 X N H NCO2Me 210 2 3 In the end,

Part One Strained Heterocycles in the Synthesis of …...anticancer activity [19, 20] 7 Mitomycin K O MeO Me O OMe N Streptomyces verticillatus [17c] Antibacterial, anticancer activity

Revision of the Cramer Decision Tree - Trusted … of the Cramer Decision Tree . 2 ... • Some proposed reworking of the DT questions/routing ... MeO MeO MeO MeO OH O O

Total Synthesis of Antascomincin Bccc.chem.pitt.edu/wipf/Current Literature/Ruth_3.pdf · 2005. 5. 2. · 26 30 6 1 11 16 1 N Fmoc 6 1 CO2H fragment I O O MOMO O 26 30 MeO MeO fragment

Marte Meo Aus- und Weiterbildung · 2020-02-12 · Marte Meo Grundkurs - Marte Meo Anwender Die TeilnehmerInnen erhalten grundlegende Informationen zu Marte Meo und Sie erwerben Fähigkeiten,

CH3 OMe CH2OHfgdfg 1 1 C:\Bruker\TopSpin3.1\examdata! S29! 13C NMR (100 MHz, CDCl 3) H3C MeO N H O OH HOOH H N CH3 OMe 3b 47.589 180 160 140 120 100 80 60 40 20 ppm Plotname: --Not

cat trbottwbewneeeotrmain.nps.dbc.ous.ac.jp/web/natpro20/2-memo+.pdfEt20, 5 oc; MeMgBr Et20, -40 oc; aq I-12S04 Check Box H 3 N C02H MeO MeO EtO OMe (TsOH, cat) MeOH reflux HBr (cat)

A p. 4/ P. 12 MeO OH OMe (1) OH CH3 Ñ02 (b) IUPAC (c) Newman (2) KW-4490 OMe OMe (a) (b) (c) (d) (e) OMe OH OH C02Et OMe C02Et Cl AIC13 OMe NC ... P. 5/ P. 12 6- y y (Glucose phosphate

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users.ox.ac.ukusers.ox.ac.uk/~dplb0149/lecture/RingCourseHO3.pdf · MeO Mechanism NaO OMe OMe ACYLOIN CONDENSATION e OH Nao e Nao Xylene, Dimerisation - 2 MeO- R OMe OMe OMe OH enol

MeO2C CO2Me NiNaI (60 mol%) DMF, 60 C ultrasounds OTf 82% yield 1971 Semmelhack Ni(COD)2 Chem. Lett. 1986, 407. MeO MeO OMe Timeline2 Percec1 Ni Chemistry Timeline Sulfonate Highlights

Rearrangements and Reactive Intermediatesburton.chem.ox.ac.uk/handout-4.pdf · Rearrangements and Reactive Intermediates 71 MeO MeOH R OMe O O MeO Me 䡧 overall in the Favorskii

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