000 | 01263nam a22002777a 4500 | ||
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003 | ZW-GwMSU | ||
005 | 20250311082249.0 | ||
008 | 250311b |||||||| |||| 00| 0 eng d | ||
022 | _a09743626 | ||
040 |
_aMSU _bEnglish _cMSU _erda |
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050 | 0 | 0 | _aQD31 JOU |
100 | 1 |
_aKotha, S. _eauthor |
|
245 | 1 | 0 |
_aDiversity oriented approach to polycyclics via cross-enyne metathesis and Diels–Alder reaction as key steps _ccreated by S. Kotha, Vittal Seema, Shaibal Banerjee and Mrityunjay Kumar Dipak |
264 | 1 |
_aBangalore : _bSpringer, _c2015. |
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336 |
_2rdacontent _atext _btxt |
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337 |
_2rdamedia _aunmediated _bn |
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338 |
_2rdacarrier _avolume _bnc |
||
440 |
_aJournal of chemical sciences _vVolume 127, number 1, |
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520 | 3 | _aPolycyclics containing biaryls have been prepared via application of cross-enyne metathesis and the Diels −Alder reaction. Here, ethylene and 1,5-hexadiene were used as a cross-coupling partners to generate key diene intermediates. | |
650 |
_aDiversity-oriented synthesis _vAryl acetylenes _xMetathesis |
||
700 | 1 |
_aSeema, Vittal _eco author |
|
700 | 1 |
_aBanerjee, Shaibal _eco author |
|
700 | 1 |
_aDipak, Mrityunjay Kumar _eco author |
|
856 | _uhttps://doi.org/10.1007/s12039-015-0765-6 | ||
942 |
_2lcc _cJA |
||
999 |
_c169232 _d169232 |