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Volumn 639, Issue 7, 2013, Pages 1205-1213

1,1-carboboration of dialkynyltin compounds using triorganoboranes of greatly different lewis acid strength. 1,4-stannabora-cyclohexa-2,5-dienes and characterization of zwitterionic intermediates

Author keywords

Organotin compounds; Alkynes; 1, 1 Carboboration; Side on 2 coordination; Tin; NMR; X ray spectroscopy

Indexed keywords


EID: 84878937131     PISSN: 00442313     EISSN: 15213749     Source Type: Journal    
DOI: 10.1002/zaac.201300007     Document Type: Article
Times cited : (14)

References (58)
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    • Crystallographic data (excluding structure factors) for the structures in this paper have been deposited with the Cambridge Crystallographic Data Centre, CCDC, 12 Union Road, Cambridge CB21EZ, UK. Copies of the data can be obtained free of charge on quoting the depository numbers CCDC-913804 (11a at 133 K) and CCDC-913805 (12a at 133 K) (Fax: +44-1223-336-033; E-Mail: deposit@ccdc.cam.ac. uk
    • Crystallographic data (excluding structure factors) for the structures in this paper have been deposited with the Cambridge Crystallographic Data Centre, CCDC, 12 Union Road, Cambridge CB21EZ, UK. Copies of the data can be obtained free of charge on quoting the depository numbers CCDC-913804 (11a at 133 K) and CCDC-913805 (12a at 133 K) (Fax: +44-1223-336-033; E-Mail: deposit@ccdc.cam.ac. uk, http://www.ccdc.cam.ac.uk).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.