A relative extrusibility scale and its application to the thermal fragmentation patterns of 5-membered ring diazenes

1981 ◽  
Vol 59 (3) ◽  
pp. 491-505 ◽  
Author(s):  
Anthony James Paine ◽  
John Warkentin

Extrusion of a stable molecular fragment (like N2, CO2, SO2, CO, etc.) is a common chemical process. Using thermodynamic additivity concepts, group values, and heat of formation data, a Relative Extrusibility Scale (ΔHex0) has been defined for these fragmentations:[Formula: see text]Twenty-four such extrusions spanning 150 kcal mol−1 have been compiled. Typical values include N2 (−42.0), CO2 (−2.6), HCN (13.8), CO (15.4), H2CO (18.3), C2H4 (32.2), and 1CH2 (109). Among other theoretical and mechanistic applications, this list should be useful when designing synthetic routes involving extrusion reactions.In a particularly effective illustration of the usefulness of the scale, it rationalizes, for the first time, the variety of product types obtained from thermolyses of 14 different kinds of 5-membered ring diazenes. Heat of formation data on most of these compounds do not exist and they contain such sufficiently complicated functional group arrangements that most of the thermodynamic group equivalents are also unknown. This problem can be circumvented by thermodynamic cycles based on the Relative Extrusibility Scale, suitable models, and interfragment resonance corrections. Within an error framework of less than ± 5 kcal mol−1, enthalpy estimates are sufficiently accurate to give heats of reaction capable of predicting which of the potential fragmentation routes actually occur. Formation of a 3-membered ring must be exothermic by at least 30 kcal mol−1 to contribute to the products, but 3-piece fragmentation and 1,3-dipolar cycloreversion will contribute to the observed products when the process is either thermoneutral or exothermic. The unimportance of entropy is also discussed.

2020 ◽  
Author(s):  
Shunya Ohuchi ◽  
Hiroki Koyama ◽  
Hiroki Shigehisa

A catalytic synthesis of cyclic guanidines, which are found in many biologically active compounds and natu-ral products, was developed, wherein transition-metal hydrogen atom transfer and radical-polar crossover were employed. This mild and functional-group tolerant process enabled the cyclization of alkenyl guanidines bearing common protective groups, such as Cbz and Boc. This powerful method not only provided the common 5- and 6-membered rings but also an unusual 7-membered ring. The derivatization of the products afforded various heterocycles. We also investigated the se-lective cyclization of mono-protected or hetero-protected (TFA and Boc) alkenyl guanidines and their further derivatiza-tions.


2019 ◽  
Author(s):  
Caleb Karmel ◽  
Zhewei Chen ◽  
John Hartwig

We report a new system for the silylation of aryl C-H bonds. The combination of [Ir(cod)(OMe)]<sub>2</sub> and 2,9-Me<sub>2</sub>-phenanthroline (2,9-Me<sub>2</sub>phen) catalyzes the silylation of arenes at lower temperatures and with faster rates than those reported previously, when the hydrogen byproduct is removed, and with high functional group tolerance and regioselectivity. Inhibition of reactions by the H<sub>2</sub> byproduct is shown to limit the silylation of aryl C-H bonds in the presence of the most active catalysts, thereby masking their high activity. Analysis of initial rates uncovered the high reactivity of the catalyst containing the sterically hindered 2,9-Me<sub>2</sub>phen ligand but accompanying rapid inhibition by hydrogen. With this catalyst, under a flow of nitrogen to remove hydrogen, electron-rich arenes, including those containing sensitive functional groups, undergo silylation in high yield for the first time, and arenes that underwent silylation with prior catalysts react over much shorter times with lower catalyst loadings. The synthetic value of this methodology is demonstrated by the preparation of key intermediates in the synthesis of medicinally important compounds in concise sequences comprising silylation and functionalization. Mechanistic studies demonstrate that the cleavage of the aryl C-H bond is reversible and that the higher rates observed with the 2,9-Me<sub>2</sub>phen ligand is due to a more thermodynamically favorable oxidative addition of aryl C-H bonds.


2021 ◽  
Author(s):  
Shi-Ping Wu ◽  
Dong-Kai Wang ◽  
Qing-Qing Kang ◽  
Guo-Ping Ge ◽  
Hongxing Zheng ◽  
...  

A novel sulfonyl radical triggered selective iodosulfonylation and bicyclizations of 1,6-dienes has been described for the first time. High selectivity and efficiency, mild reaction conditions, excellent functional group compatibility, and...


Author(s):  
Fabian Pfrengle ◽  
Hans-Ulrich Reissig

A stereodivergent synthesis of enantiopure 3,6-dihydro-2H-pyrans is presented. The addition of lithiated enol ethers to carbohydrate-derived nitrones afforded syn- or anti-configured hydroxylamine derivatives 4a–d that were cyclized under Lewis acidic conditions to yield functionalized dihydropyrans cis- or trans-5a–d containing an enol ether moiety. This functional group was employed for a variety of subsequent reactions such as dihydroxylation or bromination. Bicyclic enol ether 19 was oxidatively cleaved to provide the highly functionalized ten-membered ring lactone 20. The synthesized enantiopure aminopyrans 24, 26, 28 and 30 can be regarded as carbohydrate mimetics. Trimeric versions of 24 and 28 were constructed via their attachment to a tricarboxylic acid core.


2020 ◽  
Author(s):  
Anna Baranova ◽  
Alexey Chistov ◽  
Maxim Shuvalov ◽  
Anton Tyurin ◽  
Mikhail Biryukov ◽  
...  

Nonribosomal cyclopeptide cyclosporin A (CsA), produced by fungus <i>Tolypocladium inflatum</i>, is an extremely important immunosuppressive drug used in organ transplantations and for therapy of autoimmune diseases. Here we report for the first time production of CsA, along with related cyclosporins B and C, by <i>Tolypocladium inflatum </i>strains of marine origin (White Sea). Cyclosporins A–C contain an unusual amino acid, (4<i>R</i>)-4-((<i>E</i>)-2-butenyl)-4,<i>N</i>-dimethyl-l-threonine (MeBmt), and are prone to isomerization to non-active isocyclosporine by N→O acyl shift of valine connected to MeBmt in acidic conditions. CsA and isoCsA are not distinguishable in MS analysis of [M+H]<sup>+</sup> ions due to the rapid [CsA+H]<sup>+</sup>→[isoCsA+H]<sup>+</sup> conversion. We found that the N→O acyl shift is completely suppressed in cyclosporine [M+2H]<sup>2+</sup> ions, and their MS/MS fragmentation can be used for rapid and unambiguous analysis of cyclosporins and isocylosporins. The fragmentation patterns of [CyA+2H]<sup>2+</sup> and [isoCyA+2H]<sup>2+</sup> ions were analyzed and explained. The developed approach could be useful for MS analysis of other peptides containing β-hydroxy-α-amino acids.


1991 ◽  
Vol 235 ◽  
Author(s):  
S. L. Lai ◽  
Z. J. Zhang ◽  
J. R. Ding ◽  
B. X. Liu

ABSTRACTAmorphization behavior was studied for the Y-Ti system, which has rather positive heat of formation being around + 22 kJ/mol, by room temperature 360 keV xenon ion mixing of YxTi100−xmultilayered films to various doses, ranging from 7×1014 to 1×1016 xe/cm2 Single and uniform amorphous phase was obtained in a narrow composition region, i.e. x=65 to 75, after ion mixing to the relevant doses. Moreover, a metastable fee crystalline Y-Ti phase was observed, for the first time, in this system. The crystalline lattice constant of the metastable phase was determined to be 4.012 Å. The re-crystallization temperature of the formed amorphous alloy was found out to be 600°C by in situ transmission electron microscope annealing as well as by vacuum furnace experiments. Possible interpretation is also discussed by comparing the experimental results with those proposed models for predicting glass forming ability.


2005 ◽  
Vol 77 (12) ◽  
pp. 2029-2032 ◽  
Author(s):  
Eric Block ◽  
Evgeny V. Dikarev ◽  
Jin Jin ◽  
Bo Li ◽  
Marina A. Petrukhina ◽  
...  

Recent chemistry of four-membered ring selenium compounds is reviewed followed by a summary of work in our laboratories in this area. 2-Thia-6-selenaspiro[3.3]heptane has been synthesized for the first time. X-ray structures for the latter compound as well as for 2,6-dithiaspiro[3.3]heptane and 2,6-diselenaspiro[3.3]heptane have been determined. These compounds are useful as "rigid-rod" ligands for coordination to transition-metal complexes.


2020 ◽  
Vol 7 (18) ◽  
pp. 2612-2617
Author(s):  
Wenhao Dai ◽  
Chunpu Li ◽  
Yichu Liu ◽  
Xu Han ◽  
Xingjun Li ◽  
...  

An efficient approach to obtain saturated seven-membered ring containing three heteroatoms has been developed by using a palladium-catalyzed [4 + 3] dearomatizing cycloaddition. This approach features mild conditions and good functional group tolerance.


Molecules ◽  
2019 ◽  
Vol 24 (5) ◽  
pp. 960 ◽  
Author(s):  
Lei Peng ◽  
Xiaofei Zhang ◽  
Chunhao Yang

Bisindolyl alkaloids represent a large family of natural and synthetic products that display various biological activities. Among the bisindole compounds, 6,7,12,13-tetrahydro-5H-cyclohepta[2,1-b:3,4-b’]diindoles have received little attention. Only two methods have been developed for the construction of the 6,7,12,13-tetrahydro-5H-cyclohepta[2,1-b:3,4-b’]diindole scaffold thus far, including the classical Fischer indole synthesis conducted by reacting indole-fused cycloheptanone and hydrazines, and the condensation reaction to build the seven-membered ring. Here, we report for the first time a new route to synthesize 6,7,12,13-tetrahydro-5H-cyclohepta[2,1-b:3,4-b’]diindoles through intramolecular oxidative coupling of 1,3-di(1H-indol-3-yl)propanes in the presence of PIFA, DDQ and TMSCl with moderate to excellent yields.


Synlett ◽  
2018 ◽  
Vol 29 (07) ◽  
pp. 908-911 ◽  
Author(s):  
K. Babu ◽  
Arramshetti Venkanna ◽  
Borra Poornima ◽  
Bandi Siva ◽  
B. Babu

A stereoselective synthesis of the dibenzocyclooctadiene ­lignan core of the natural product schisandrene is described. Starting from readily available gallic acid, the synthetic strategy involves Suzuki–Miyaura cross-coupling, Stille reaction, and ring-closing metathesis (RCM) in the reaction sequence. The required asymmetric center at C-7′ was established by an asymmetric reduction of a keto compound using the Corey–Bakshi–Shibata (CBS) catalyst. In our approach, the eight-membered ring was achieved by RCM for the first time.


Sign in / Sign up

Export Citation Format

Share Document