Rhodium(III)-catalyzed oxidative annulation of isoquinolones with allyl alcohols: synthesis of isoindolo[2,1-b]isoquinolin-5(7H)-ones

Organic & Biomolecular Chemistry ◽

10.1039/d1ob02305e ◽

2022 ◽

Author(s):

Jinyuan Jiang ◽

Jidan Liu ◽

Zhenke Yang ◽

Jieying Zheng ◽

Xin Tian ◽

...

Keyword(s):

Allyl Alcohols

An efficient rhodium(III)-catalyzed direct C-H oxidative annulation of isoquinolones with allyl alcohols as C1 synthons has been successfully developed. This protocol enables the straightforward synthesis of structurally diverse isoindolo[2,1-b]isoquinolin-5(7H)-ones with...

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ChemInform Abstract: COHALOGENATION OF OLEFINS: APPLICATION TO THE SYNTHESIS OF ALLYL ALCOHOLS

Chemischer Informationsdienst ◽

10.1002/chin.198421151 ◽

1984 ◽

Vol 15 (21) ◽

Author(s):

J. RODRIGUEZ ◽

J.-P. DULCERE ◽

M. BERTRAND

Keyword(s):

Allyl Alcohols

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ChemInform Abstract: Fast and Highly Regioselective Allylation of Indole and Pyrrole Compounds by Allyl Alcohols Using Ru-Sulfonate Catalysts.

ChemInform ◽

10.1002/chin.200902127 ◽

2009 ◽

Vol 40 (2) ◽

Author(s):

Alexey B. Zaitsev ◽

Stefan Gruber ◽

Pascal A. Pluess ◽

Paul S. Pregosin ◽

Luis F. Veiros ◽

...

Keyword(s):

Allyl Alcohols

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Synthesis of 2-allyl-2,3-dihydro-1H-indol-3-ones using in situ Claisen rearrangement of 2,3-dihydro-1H-indol-3-ones with allyl alcohols

Journal of the Chemical Society Perkin Transactions 1 ◽

10.1039/p19960000729 ◽

1996 ◽

pp. 729 ◽

Cited By ~ 15

Author(s):

Tomomi Kawasaki ◽

Kouhei Masuda ◽

Yasutaka Baba ◽

Romi Terashima ◽

Kana Takada ◽

...

Keyword(s):

Claisen Rearrangement ◽

Allyl Alcohols

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A versatile route to silylsubstituted ketones by rhodium catalyzed isomerization of silylated allyl alcohols

Tetrahedron Letters ◽

10.1016/s0040-4039(01)80021-6 ◽

1984 ◽

Vol 25 (7) ◽

pp. 769-770 ◽

Cited By ~ 29

Author(s):

Susumu Sato ◽

Hisashi Okada ◽

Isamu Matsuda ◽

Yusuke Izumi

Keyword(s):

Allyl Alcohols

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Immobilized vanadium amino acid Schiff base complex on Al-MCM-41 as catalyst for the epoxidation of allyl alcohols

Reaction Kinetics Mechanisms and Catalysis ◽

10.1007/s11144-011-0340-1 ◽

2011 ◽

Vol 104 (1) ◽

pp. 197-209 ◽

Cited By ~ 18

Author(s):

Elham Zamanifar ◽

Faezeh Farzaneh

Keyword(s):

Schiff Base ◽

Amino Acid ◽

Schiff Base Complex ◽

Base Complex ◽

Allyl Alcohols ◽

Amino Acid Schiff Base ◽

Mcm 41

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Asymmetric Synthesis of Baylis–Hillman-Type Allyl Alcohols via a Chiral Acetylenic Ester Titanium Alkoxide Complex

Angewandte Chemie ◽

10.1002/1521-3757(20000915)112:18<3428::aid-ange3428>3.0.co;2-e ◽

2000 ◽

Vol 112 (18) ◽

pp. 3428-3430 ◽

Cited By ~ 1

Author(s):

Daisuke Suzuki ◽

Hirokazu Urabe ◽

Fumie Sato

Keyword(s):

Asymmetric Synthesis ◽

Titanium Alkoxide ◽

Acetylenic Ester ◽

Allyl Alcohols

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ChemInform Abstract: Stereoselectivity in the Ortho Ester Claisen Rearrangements of the E and Z Isomers of γ-(1,3-Dioxan-4-yl)allyl Alcohols.

ChemInform ◽

10.1002/chin.199036213 ◽

1990 ◽

Vol 21 (36) ◽

Author(s):

K. TADANO ◽

M. MINAMI ◽

S. OGAWA

Keyword(s):

Ortho Ester ◽

Claisen Rearrangements ◽

E And Z Isomers ◽

Allyl Alcohols

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Iridium(III)-Catalyzed Two-Fold C−H Alkylation of BINOLs with Allyl Alcohols

Organic Chemistry Frontiers ◽

10.1039/d1qo01486b ◽

2022 ◽

Author(s):

Lin Dong ◽

Hao Liu ◽

Wei Chi ◽

Meng-Ling Lin

Keyword(s):

Rapid Synthesis ◽

Allyl Alcohols

Ir(III)-catalyzed C−H alkylation of BINOL units has been well examined by allyl alcohols as coupling partners. Under the advantage of pyridine guiding group, the efficient protocol allows the rapid synthesis...

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