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Volumn 118, Issue 50, 1996, Pages 12588-12597

Reactions and reactivity of acyloxycarbenes

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPROPANE DERIVATIVE; DIKETONE; KETONE;

EID: 0030453602     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja9626244     Document Type: Article
Times cited : (29)

References (73)
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    • note
    • Structures 28a-c and 28aTS-cTS were reoptimized with electron correlation included at the MP2/6-31G* level. The MP2/6-31G*//6-31G*-optimized structures are not dramatically different from those obtained at the HF/6-31G*//6-31G* level, in particular conformer 28a-Z does persist as minimum at this computational level.
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    • note
    • 50
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    • note
    • All diazirine yields were determined by NMR and are based on consumed bromodiazirine.
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    • note
    • max of 9 is erroneously given as 336 instead of 364 nm.
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    • In view of the higher field appearance of the OOCMe singlet and lower field appearance of the upfield cyclopropyl Me singlet of the major isomer, this isomer is likely to be of the syn-OAc configuration. For NMR shielding effects in phenylcyclopropanes, see: Closs, G. L.; Moss, R. A. J. Am. Chem. Soc. 1964, 86, 4042.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.