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Volumn 120, Issue 4, 1998, Pages 722-733

Kinetic addition of nucleophiles to η3-propargyl rhenium complexes occurs at the central carbon to produce rhenacyclobutenes

Author keywords

[No Author keywords available]

Indexed keywords

METAL COMPLEX; RHENACYCLOBUTENE; RHENIUM; RHENIUM COMPLEX; UNCLASSIFIED DRUG;

EID: 0032481404     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja9729847     Document Type: Article
Times cited : (68)

References (109)
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    • note
    • Extension of this methodology to the tert-butyl-substituted and the unsubstituted propargyl complexes 3a and 3c was unsuccessful.
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    • note
    • 3-propargyl complex 3a did not produce products with NMR resonances consistent with the formation of a metallacyclobutene and/or an alkyne complex analogous to the DMAP complexes 22a or 23.
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    • 1.4
    • anti coupling is consistent with the "W" relative geometry of the syn protons, which is more favorable for the transmission of coupling information.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.