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Volumn 4, Issue 10, 2014, Pages 3605-3611

Correction to Enhanced Catalytic Performance of Indenediide Palladium Pincer Complexes for Cycloisomerization: Efficient Synthesis of Alkylidene Lactams (ACS Catal. (2014) 4 (3605-3611) 10.1021/cs5010322);Enhanced catalytic performance of indenediide palladium pincer complexes for cycloisomerization: Efficient synthesis of alkylidene lactams

Author keywords

cycloisomerization; lactams; metal ligand cooperation; noninnocent ligand; palladium; pincer complexes

Indexed keywords

AMIDES; CATALYST ACTIVITY; ISOMERIZATION; LIGANDS; PALLADIUM; SYNTHESIS (CHEMICAL);

EID: 84907852588     PISSN: None     EISSN: 21555435     Source Type: Journal    
DOI: 10.1021/acscatal.6b00198     Document Type: Erratum
Times cited : (52)

References (95)
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    • Chaplan, S. R.; Dubin, A. E.; Lee, D. H.; Liu, C. PCT Int. Appl. WO 0100408 A2 20021219, 2002; p 133.
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    • This scheme is supported by D labeling studies using N-deuterated 1a. Although some of the D labeling was lost during cyclization (N-deuterated sulfonamides are known to be labile, see: McKinney Brooner, R. E.; Widenhoefer, R. A. Chem.-Eur. J. 2011, 17, 6170-6178), the resulting lactam 2a displays D labeling in the position trans to N (80%), but none in the position cis to N (see Figures S11 and S12 of the Supporting Information)
    • (2011) Chem.-Eur. J. , vol.17 , pp. 6170-6178
    • McKinney Brooner, R.E.1    Widenhoefer, R.A.2
  • 95
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    • 31 P NMR), while the corresponding Ph-substituted Pd carbonyl complex becomes minor (1/3 mixture in favor of trimer Ic). See also: Bolliger, J. L.; Blacque, O.; Frech, C. M. Angew. Chem., Int. Ed. 2007, 46, 6514-6517
    • (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 6514-6517
    • Bolliger, J.L.1    Blacque, O.2    Frech, C.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.