✦ LIBER ✦

A mass-spectral study of exo- and endo-2-norbornyl bromide and exo and endo-8-bromobicyclo[3.2.1]octane by photoionization

✍ Scribed by D. C. DeJongh; S. R. Shrader; R. G. Isakson; N. A. LeBel; J. H. Beynon

Publisher: John Wiley and Sons
Year: 1969
Tongue: English
Weight: 195 KB
Volume: 2
Category: Article
ISSN: 1076-5174
DOI: 10.1002/oms.1210020908

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Azabrendanes. III. Synthesis of stereois

Azabrendanes. III. Synthesis of stereoisomeric exo- and endo-5-acylaminomethyl-exo-2,3-epoxybicyclo[2.2.1]heptanes and their reduction by lithium aluminum hydride

✍ Lilija I. Kasyan; Igor N. Tarabara; Oxana A. Savel'yeva; Andrey O. Kasyan 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 121 KB

## Abstract A number of stereoisomeric N‐[aryl(alkyl, cycloalkyl)carbonyl]‐exo(endo)‐5‐aminomethylbicyclo[2.2.1]hept‐2‐enes have been synthesized from bicyclo[2.2.1]hept‐2‐en‐exo(endo)‐5‐carbonitrile via reduction of the latter by lithium aluminum hydride and subsequent reactions of the resulting a

ChemInform Abstract: Azabrendanes. Part

ChemInform Abstract: Azabrendanes. Part 3. Synthesis of Stereoisomeric exo- and endo-5-Acylaminomethyl-exo-2,3-epoxybicyclo[2.2.1]heptanes and Their Reduction by Lithium Aluminum Hydride.

✍ Lilija I. Kasyan; Igor N. Tarabara; Oxana A. Savel'yeva; Andrey O. Kasyan 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 1 views

Synthesis and Unambiguous Stereochemical

Synthesis and Unambiguous Stereochemical Determination of 1-exo- and 1-endo-1-Aryl-1,2,2a,8b-tetrahydro-3H-benzo[b]cyclobuta[d]pyran-3-ones.

✍ Masayuki Yamashita; Yadav Navnath Dnyanoba; Masaki Nagahama; Tomoki Inaba; Yuka 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 27 KB 👁 1 views

Nucleophilic addition to C,C double bond

Nucleophilic addition to C,C double bonds. III. Chemical reactivity of 1endo, 4endo: 5exo, 8exo-dimethano-1,2,3,4,4a,5,8,8a-octahydronaphthalen-10syn-ol and X-ray structure analysis of its p-nitrobenzoate

✍ Rolland A. Pfund; W. Bernd Schweizer; Camille Ganter 📂 Article 📅 1980 🏛 John Wiley and Sons 🌐 German ⚖ 400 KB

## Abstract The title compound **1** is a further example of an olefinic alcohol that undergoes ether formation under basic conditions **(→ 3)** although the double bond is not activated by an electron‐attracting group. This unusual reactivity is due to steric compression, which is increased in the

ChemInform Abstract: Desymmetrization by

ChemInform Abstract: Desymmetrization by Ring-Closing Metathesis Leading to 6,8-Dioxabicyclo[3.2.1]octanes: A New Route for the Synthesis of (+)-exo- (VI) and endo-Brevicomin (XI).

✍ Steven D. Burke; Norbert Mueller; Christopher M. Beaudry 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 2 views

Electron impact and chemical ionization

Electron impact and chemical ionization mass spectra of norbornane/ene di-exo and di-endo-fused 1,3-oxazin-2(1H)-ones and 1,3-oxazine-2(1H)-thiones

✍ Tuula Partanen; Pirjo Vainiotalo; Géza Stájer; Gábor Bernáth; Kalevi Pihlaja 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 448 KB

Mass spectral fragmentations of four norbornaneleoe di-em-and di-endo-fused 1,3-oxazin-2( lH)-ones and four 1,3-oxazine-2(1H)-thiones were examined by means of metastable ion analysis, the collision-induced dissociation technique and exact mass measurement. Under electron impact (EI) conditions all