An Efficient and Practical Synthesis of Dibenzo[d,f][1,3]-dioxepines from 2,2′-Dihydroxybiphenyl with Terminal Alkynes Catalyzed by Lewis Acid TiCl4

Haisheng Wu; Jin Yang; Lei Wang

doi:10.1002/cjoc.201190225

An Efficient and Practical Synthesis of Dibenzo[d,f][1,3]-dioxepines from 2,2′-Dihydroxybiphenyl with Terminal Alkynes Catalyzed by Lewis Acid TiCl4

Chinese Journal of Chemistry ◽

10.1002/cjoc.201190225 ◽

2011 ◽

Vol 29 (6) ◽

pp. 1211-1215 ◽

Cited By ~ 2

Author(s):

Haisheng Wu ◽

Jin Yang ◽

Lei Wang

Keyword(s):

Lewis Acid ◽

Terminal Alkynes ◽

Practical Synthesis

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ChemInform Abstract: An Efficient and Practical Synthesis of Dibenzo[b,f][1,3]dioxepines from 2,2′-Dihydroxybiphenyl with Terminal Alkynes Catalyzed by Lewis Acid TiCl4.

ChemInform ◽

10.1002/chin.201145169 ◽

2011 ◽

Vol 42 (45) ◽

pp. no-no

Author(s):

Haisheng Wu ◽

Jin Yang ◽

Lei Wang

Keyword(s):

Lewis Acid ◽

Terminal Alkynes ◽

Practical Synthesis

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ChemInform Abstract: Simple and Practical Synthesis of Pyrano- and Furano[3,2-c]quinoline Derivatives under Non-Lewis Acid Catalysis.

ChemInform ◽

10.1002/chin.201306111 ◽

2013 ◽

Vol 44 (6) ◽

pp. no-no

Author(s):

Rui Huan Liu ◽

Xin Yu ◽

Liang Hu ◽

Nie Fang Yu

Keyword(s):

Lewis Acid ◽

Acid Catalysis ◽

Quinoline Derivatives ◽

Lewis Acid Catalysis ◽

Practical Synthesis

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Front Cover Picture: Zinc/Indium Bimetallic Lewis Acid Relay Catalysis for Dehydrogenative Silylation/Hydrosilylation Reaction of Terminal Alkynes with Bis(hydrosilane)s (Adv. Synth. Catal. 19/2020)

Advanced Synthesis & Catalysis ◽

10.1002/adsc.202000968 ◽

2020 ◽

Vol 362 (19) ◽

pp. 3925-3925

Author(s):

Tomohiro Tani ◽

Yudai Sohma ◽

Teruhisa Tsuchimoto

Keyword(s):

Lewis Acid ◽

Terminal Alkynes ◽

Front Cover ◽

Hydrosilylation Reaction

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Silver-catalyzed carbon–selenium cross-coupling using N-(phenylseleno)phthalimide: an alternate approach to the synthesis of organoselenides

Canadian Journal of Chemistry ◽

10.1139/cjc-2016-0427 ◽

2017 ◽

Vol 95 (1) ◽

pp. 51-56 ◽

Cited By ~ 3

Author(s):

Nirmalya Mukherjee ◽

Subhajit Pal ◽

Amit Saha ◽

Brindaban C. Ranu

Keyword(s):

Lewis Acid ◽

Cross Coupling ◽

Terminal Alkynes ◽

Organoboronic Acids

Silver(I) catalyzed phenylselenylation of terminal alkynes and organoboronic acids has been demonstrated using N-(phenylseleno)phthalimide as an electrophilic SePh donor. A wide variety of terminal alkynes and organoboronic acids are selenylated efficiently to produce the corresponding alkynyl and diaryl selenides, respectively, in good yields. Silver(I) acts as a Lewis acid in this process.

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ChemInform Abstract: A Simple and Practical Synthesis of (+)-2-Bromobicyclo(2.2.1)hept-5- ene-2-carboxaldehyde via Chiral Lewis Acid Catalyzed (4 + 2) Cycloaddition.

ChemInform ◽

10.1002/chin.199624063 ◽

2010 ◽

Vol 27 (24) ◽

pp. no-no

Author(s):

G. E. KECK ◽

D. KRISHNAMURTHY

Keyword(s):

Lewis Acid ◽

Chiral Lewis Acid ◽

Practical Synthesis ◽

Acid Catalyzed

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Lewis Acid Promoted Alkynylation of Imines with Terminal Alkynes: Simple, Mild and Efficient Preparation of Propargylic Amines.

ChemInform ◽

10.1002/chin.200349084 ◽

2003 ◽

Vol 34 (49) ◽

Author(s):

Biao Jiang ◽

Yu-Gui Si

Keyword(s):

Lewis Acid ◽

Terminal Alkynes

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Practical synthesis of functionalized terminal alkynes, 3,3,3-triethoxypropyne and ketal protected prop-2-ynones

Synthetic Communications ◽

10.1080/00397911.2017.1376334 ◽

2017 ◽

Vol 47 (24) ◽

pp. 2342-2351 ◽

Cited By ~ 3

Author(s):

Abdullah Karanfil ◽

Mustafa Eskici

Keyword(s):

Terminal Alkynes ◽

Practical Synthesis

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Zinc/Indium Bimetallic Lewis Acid Relay Catalysis for Dehydrogenative Silylation/Hydrosilylation Reaction of Terminal Alkynes with Bis(hydrosilane)s

Advanced Synthesis & Catalysis ◽

10.1002/adsc.202000501 ◽

2020 ◽

Vol 362 (19) ◽

pp. 4098-4108

Author(s):

Tomohiro Tani ◽

Yudai Sohma ◽

Teruhisa Tsuchimoto

Keyword(s):

Lewis Acid ◽

Terminal Alkynes ◽

Hydrosilylation Reaction

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Lewis-Acid-Catalysed Reaction of 3-Hydroxy-2-oxindoles with Terminal Alkynes: Synthetic Approaches to the Pyrroloindoline Alkaloids

European Journal of Organic Chemistry ◽

10.1002/ejoc.201700507 ◽

2017 ◽

Vol 2017 (21) ◽

pp. 3078-3091 ◽

Cited By ~ 7

Author(s):

Lakshmana K. Kinthada ◽

K. Naresh Babu ◽

Dikshaa Padhi ◽

Alakesh Bisai

Keyword(s):

Lewis Acid ◽

Terminal Alkynes ◽

Catalysed Reaction ◽

Synthetic Approaches

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Ring-opening formal hetero-[5+2] cycloaddition of 1-tosyl-2,3-dihydro-1H-pyrroles with terminal alkynes: entry to 1-tosyl-2,3-dihydro 2,3-dihydro-1H-azepines

Chemical Communications ◽

10.1039/c9cc05082e ◽

2019 ◽

Vol 55 (75) ◽

pp. 11295-11298 ◽

Cited By ~ 1

Author(s):

Ming-Bo Zhou ◽

Rui Pi ◽

Fan Teng ◽

Yang Li ◽

Jin-Heng Li

Keyword(s):

Lewis Acid ◽

Ring Opening ◽

Bond Cleavage ◽

Terminal Alkynes ◽

Acid Catalyzed

Lewis acid-catalyzed formal hetero-[5+2] cycloaddition of 2,3-dihydro-1H-pyrroles with alkynes through C(sp2)–N bond cleavage toward 2,3-dihydro-1H-azepines is described.

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