메뉴 건너뛰기




Volumn 64, Issue 15, 2008, Pages 3331-3336

Combined directed ortho-metalation, remote metalation, and Stille cross-coupling strategies. Concise stereoselective synthesis of polysubstituted 9H-fluoren-9-ones

Author keywords

Benzoic acids; ortho and Remote metalations; Stille reaction

Indexed keywords

4 CHLORO 9H FLUOREN 9 ONE; 5 CHLORO 1 METHOXY 9H FLUOREN 9 ONE; 5 CHLORO 2 METHOXY 9H FLUOREN 9 ONE; 5 CHLORO 2 METHYL 9H FLUOREN 9 ONE; BENZOIC ACID; CARBOXYLIC ACID DERIVATIVE; FLUORENONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 39649119396     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.01.122     Document Type: Article
Times cited : (16)

References (71)
  • 10
    • 39649106389 scopus 로고    scopus 로고
    • note
    • 2′ refers to the remote 2′-position.
  • 12
    • 39649124990 scopus 로고    scopus 로고
    • Reviews on reactions of organolithium compounds with alkali metal alkoxides and reactions of superbases:
    • Reviews on reactions of organolithium compounds with alkali metal alkoxides and reactions of superbases:
  • 14
    • 0034755906 scopus 로고    scopus 로고
    • and references cited therein
    • Schlosser M. Eur. J. Org. Chem. (2001) 3975-3984 and references cited therein
    • (2001) Eur. J. Org. Chem. , pp. 3975-3984
    • Schlosser, M.1
  • 17
    • 39649120604 scopus 로고    scopus 로고
    • Metalation reactions of unprotected benzoic acids:
    • Metalation reactions of unprotected benzoic acids:
  • 20
    • 39649120605 scopus 로고    scopus 로고
    • Recent references:
    • Recent references:
  • 31
    • 39649116491 scopus 로고    scopus 로고
    • Reviews:
    • Reviews:
  • 37
    • 0036054279 scopus 로고    scopus 로고
    • Triorganotin esters of carboxylic acids possess high biocidal activity against fungi and bacteria. They are therefore used on a large scale as biocidally active ingredients in many materials and as preservatives or disinfectants. See: and references cited therein
    • Triorganotin esters of carboxylic acids possess high biocidal activity against fungi and bacteria. They are therefore used on a large scale as biocidally active ingredients in many materials and as preservatives or disinfectants. See:. Gielen M. Appl. Organomet. Chem. 16 (2002) 481-494 and references cited therein
    • (2002) Appl. Organomet. Chem. , vol.16 , pp. 481-494
    • Gielen, M.1
  • 38
    • 39649102792 scopus 로고    scopus 로고
    • Preparation of ortho-stannyl benzoic acids:
    • Preparation of ortho-stannyl benzoic acids:
  • 39
    • 39649089202 scopus 로고    scopus 로고
    • Nietzschmann, E.; Tzschach, A.; Heinicke, J.; Pape, U.; Thust, U.; Pfeiffer, H. D. Ger. (East) Patent DD268699, 1989.
    • Nietzschmann, E.; Tzschach, A.; Heinicke, J.; Pape, U.; Thust, U.; Pfeiffer, H. D. Ger. (East) Patent DD268699, 1989.
  • 41
    • 39649095905 scopus 로고    scopus 로고
    • Rheinheimer, J.; Vogelbacher, U. J.; Baumann, E.; Mislitz, U.; Westphalen, K. O.; Walter, H. World Patent WO12883A1, 1997.
    • Rheinheimer, J.; Vogelbacher, U. J.; Baumann, E.; Mislitz, U.; Westphalen, K. O.; Walter, H. World Patent WO12883A1, 1997.
  • 44
    • 39649109500 scopus 로고    scopus 로고
    • Reviews on the Stille cross-coupling reaction:
    • Reviews on the Stille cross-coupling reaction:
  • 48
    • 39649114826 scopus 로고    scopus 로고
    • Aryl-aryl bond formation by transition-metal-catalyzed direct arylation, reviews:
    • Aryl-aryl bond formation by transition-metal-catalyzed direct arylation, reviews:
  • 52
    • 39649125229 scopus 로고    scopus 로고
    • note
    • 18c


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.