The synthesis of homoisotwistanes by the tandem wessely oxidation - diels-alder reaction sequence

Tetrahedron Letters ◽

10.1016/0040-4039(91)80006-r ◽

1991 ◽

Vol 32 (35) ◽

pp. 4439-4442 ◽

Author(s):

N.K. Bhamare ◽

Thierry Granger ◽

C.R. John ◽

Peter Yates

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Reaction Sequence ◽

Diels Alder Reaction

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Synthesis of 2,3-Di- and 2,3,4-Trisubstituted Furans from 1,2-Dioxines Generated by an Enyne-RCM/Diels−Alder Reaction Sequence

The Journal of Organic Chemistry ◽

10.1021/jo050957q ◽

2005 ◽

Vol 70 (17) ◽

pp. 6995-6998 ◽

Author(s):

Young-Keun Yang ◽

Jung-Hoon Choi ◽

Jinsung Tae

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Reaction Sequence ◽

Diels Alder Reaction ◽

Trisubstituted Furans

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Synthesis of Cyclic Peroxides via Enyne-RCM/Diels-Alder Reaction Sequence

Bulletin of the Korean Chemical Society ◽

10.5012/bkcs.2004.25.9.1307 ◽

2004 ◽

Vol 25 (9) ◽

pp. 1307-1308 ◽

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Reaction Sequence ◽

Diels Alder Reaction

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Domino intermolecular and intramolecular Diels-Alder reaction sequence for expedient construction of a pentacyclic framework

Chemical Data Collections ◽

10.1016/j.cdc.2020.100404 ◽

2020 ◽

Vol 28 ◽

pp. 100404

Author(s):

K.M. Nishad ◽

C.S. Aswathi ◽

P.A. Unnikrishnan ◽

T.S. Saumya

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Reaction Sequence ◽

Diels Alder Reaction

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A New Approach to the 1-Arylnaphthalene Lignans Utilizing a Tandem Pummerer-Diels-Alder Reaction Sequence

The Journal of Organic Chemistry ◽

10.1021/jo00118a004 ◽

1995 ◽

Vol 60 (13) ◽

pp. 3938-3939 ◽

Author(s):

John E. Cochran ◽

Albert Padwa

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Reaction Sequence ◽

New Approach ◽

Diels Alder Reaction

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[4 + 2] Cycloadditions ofN-Alkenyl Iminium Ions: Structurally Complex Heterocycles from a Three-Component Diels−Alder Reaction Sequence

Journal of the American Chemical Society ◽

10.1021/ja8028153 ◽

2008 ◽

Vol 130 (29) ◽

pp. 9222-9223 ◽

Author(s):

Nihar Sarkar ◽

Abhisek Banerjee ◽

Scott G. Nelson

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Reaction Sequence ◽

Diels Alder Reaction ◽

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ChemInform Abstract: A New Approach to the 1-Arylnaphthalene Lignans Utilizing a Tandem Pummerer-Diels-Alder Reaction Sequence.

10.1002/chin.199546235 ◽

2010 ◽

Vol 26 (46) ◽

pp. no-no

Author(s):

J. E. COCHRAN ◽

A. PADWA

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Reaction Sequence ◽

New Approach ◽

Diels Alder Reaction

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ChemInform Abstract: Tandem Pummerer-Diels-Alder Reaction Sequence. A Novel Cascade Process for the Preparation of 1-Arylnaphthalene Lignans.

10.1002/chin.199639067 ◽

2010 ◽

Vol 27 (39) ◽

pp. no-no

Author(s):

A. PADWA ◽

J. E. COCHRAN ◽

C. O. KAPPE

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Cascade Process ◽

Reaction Sequence ◽

Diels Alder Reaction

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Synthesis of Cyclic Peroxides via Enyne-RCM/Diels?Alder Reaction Sequence.

10.1002/chin.200509162 ◽

2005 ◽

Vol 36 (9) ◽

Author(s):

Young-Keun Yang ◽

Susie Lee ◽

Jinsung Tae

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Reaction Sequence ◽

Diels Alder Reaction

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Synthesis of the Bicyclic Lactone Core of Leonuketal, Enabled by a Telescoped Diels–Alder Reaction Sequence

Chemistry - An Asian Journal ◽

10.1002/asia.201800903 ◽

2018 ◽

Vol 14 (8) ◽

pp. 1128-1135 ◽

Author(s):

Phillip S. Grant ◽

Margaret A. Brimble ◽

Daniel P. Furkert

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Reaction Sequence ◽

Diels Alder Reaction ◽

Bicyclic Lactone

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Homodimerization of 2H-chromenes catalyzed by Brønsted-acid derived UiO-66 MOFs

Catalysis Science & Technology ◽

10.1039/c7cy02362f ◽

2018 ◽

Vol 8 (13) ◽

pp. 3406-3413 ◽

Author(s):

Zongcheng Miao ◽

Zihao Zhou ◽

Houliang Tang ◽

Mengdie Yu ◽

Daniele Ramella ◽

...

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Bronsted Acid ◽

Brønsted Acid ◽

Reaction Sequence ◽

Diels Alder Reaction ◽

Brønsted acid UiO-66 MOFs were prepared for the efficient homo-dimerization of 2H-chromenes, which involves a tandem rearrangement/hetero-Diels–Alder reaction sequence.

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