Benz[f]isoindole

Remy, David E.; Bissett, Frank H.

doi:10.1021/jo00417a016

Cited by 13 publications

(3 citation statements)

References 10 publications

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“…To determine the effect of arene ring electronics on the neophyl-like migration, we prepared adducts 28e-g (Scheme 12) by diazotization of the appropriate aromatic amino acid derivatives in the presence of N-Boc-pyrrole. 46 Hydrogenation 43 of these adducts was conducted to give reference samples of the products of direct reduction 32e-g, as substitution of the aromatic ring was expected to affect the ratio of directly-reduced : rearranged products.…”

Section: Formation Of Xanthatementioning

confidence: 99%

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Development of two processes for the synthesis of bridged azabicyclic systems: intermolecular radical addition–homoallylic rearrangements leading to 2-azanorborn-5-enes and neophyl-type radical rearrangements to 2-azabenzonorbornanes

2003

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Section: Formation Of Xanthatementioning

confidence: 99%

“…Compound 28g was prepared according to the procedure of Remy and Bornstein and their co-workers. 46 Details can be found in the electronic supplementary information. ‡…”

Section: N-(tert-butoxycarbonyl)-14-dihydro-14-iminonaphthalene 28a 40mentioning

confidence: 99%

Development of two processes for the synthesis of bridged azabicyclic systems: intermolecular radical addition–homoallylic rearrangements leading to 2-azanorborn-5-enes and neophyl-type radical rearrangements to 2-azabenzonorbornanes

2003

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“…To determine the effect of arene ring electronics on the neophyl-like migration, we prepared adducts 3d − f (Scheme ) by diazotization of the appropriate aromatic amino acid derivatives in the presence of N -Boc pyrrole . Deoxygenation of the derived xanthates 5d − f gave the expected products 7d − f in good yields.…”

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confidence: 99%

2-Azabenzonorbornanes from 7-Azabenzonorbornanols by a Nitrogen-Directed Neophyl-Type Radical Rearrangement

2002

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The Retro–Diels–Alder Reaction PartI.CCDienophiles

Rickborn

1998

Organic Reactions

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The Diels–Alder (“DA”) reaction is so familiar to organic chemists that the retro‐Diels–Alder or retro‐diene reaction (hereafter “rDA”) requires no conceptual introduction. However, a working definition is needed to indicate the coverage of this review. The intent is to include all reported examples of the general skeletal process excluded in this chapter. Any of the atoms in the starting material (cycloadduct) may be carbon or heteroatom, and substituents on all positions are allowed. In addition, any bond order available to the element in any oxidation state is included, as well as bonding to non‐nearest neighbor atoms (bicyclics, etc.). The volume of literature required separation of this review into two parts. Part I covers all expelled C–C dienophiles, i.e. those reactions that generate a new carbon‐carbon double or triple bond in the dienophile that is formed. Part II, to appear later, covers those expelled dienophiles in which one or both atoms is a heteroatom. Certain specific topics are intentionally omitted. These are: rDA reactions invoked under mass spectral conditions; rDA reactions of polymeric substrates; Electrocyclic processes, some of which are arguably very similar to rDA reactions (these are not addressed unless needed for clarification of an rDA sequence); and a thorough discussion of homo‐rDA reactions. CAS‐Online searches resulted in ca. 1,300 references, of which ca. 900 proved pertinent to the rDA topic as defined and delimited above. Active literature searching was halted in April 1995, but occasional more recent articles are included. Over 2,500 pertinent references were eventually found. Most were obtained by perusal of primary literature (articles) and secondary sources (books and reviews). Computer based search success was limited mainly by the failure of authors or abstractors to key‐word this topic, an especially common occurrence when the expelled dienophile was a simple substance such as N 2 or CO 2 . Overall, approximately 3,500 books, chapters, reviews, articles, and abstracts were consulted in an effort to make this review as comprehensive as possible. This was done with the certainty that some pertinent literature would be missed, tempered by the view that these omissions are probably also lost to any future rational search method. Many secondary sources proved valuable not only for in‐depth discussion of certain rDA reaction types, but also for providing comparisons with related topics. To assist the reader, these secondary sources are referenced (alphabetically by first author within broad subject areas) with a title or brief note on the topic(s) addressed. The first group lists earlier reviews with primary focus on rDA reactions, followed by items of Historical/General Interest, reviews that deal with Experimental Methods, DA reactions (general and specific), reviews of Related Topics (these impinge in more or less significant ways on rDA reactions), and general treatments of Theory and Mechanism.

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Benz[f]isoindole

Cited by 13 publications

References 10 publications

Development of two processes for the synthesis of bridged azabicyclic systems: intermolecular radical addition–homoallylic rearrangements leading to 2-azanorborn-5-enes and neophyl-type radical rearrangements to 2-azabenzonorbornanes

Development of two processes for the synthesis of bridged azabicyclic systems: intermolecular radical addition–homoallylic rearrangements leading to 2-azanorborn-5-enes and neophyl-type radical rearrangements to 2-azabenzonorbornanes

2-Azabenzonorbornanes from 7-Azabenzonorbornanols by a Nitrogen-Directed Neophyl-Type Radical Rearrangement

The Retro–Diels–Alder Reaction PartI.CCDienophiles

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