메뉴 건너뛰기




Volumn 35, Issue 4, 2005, Pages 275-279

Preparation and properties of chiral spiroborate esters with an O 3BN framework

Author keywords

Chiral spiroborate ester; O3BN framework; Preparation; Properties

Indexed keywords

ALKALI METAL; BORIC ACID; ESTER DERIVATIVE; HYDROXIDE; LEWIS ACID; LEWIS BASE;

EID: 19044395813     PISSN: 15533174     EISSN: None     Source Type: Journal    
DOI: 10.1081/SIM-200055237     Document Type: Article
Times cited : (8)

References (16)
  • 1
    • 0000453908 scopus 로고
    • Asymmetric synthesis via chiral organoborane reagents
    • Brown, H. C.; Jadhav, P. K.; Mandal, A. K. Asymmetric synthesis via chiral organoborane reagents. Tetrahedron 1981, 37, 3547.
    • (1981) Tetrahedron , vol.37 , pp. 3547
    • Brown, H.C.1    Jadhav, P.K.2    Mandal, A.K.3
  • 3
    • 0035855969 scopus 로고    scopus 로고
    • Enantioselective reductions by chirally modified alumino- and borohydrides
    • Daverio, P.; Zanda, M. Enantioselective reductions by chirally modified alumino- and borohydrides. Tetrahedron: Asymmetry 2001, 12, 2225.
    • (2001) Tetrahedron: Asymmetry , vol.12 , pp. 2225
    • Daverio, P.1    Zanda, M.2
  • 4
    • 0002096855 scopus 로고
    • 1,4-Bismethanesulfonates of the stereoisomeric butane-tetraols and related compounds
    • Feit, P. W. 1,4-Bismethanesulfonates of the stereoisomeric butane-tetraols and related compounds. J. Med. Chem. 1964, 7, 14.
    • (1964) J. Med. Chem. , vol.7 , pp. 14
    • Feit, P.W.1
  • 5
    • 0009085426 scopus 로고
    • Improved preparation of diborane
    • Freeguard, G. F.; Long, L. H. Improved preparation of diborane. Chem. Ind. 1965, 471.
    • (1965) Chem. Ind. , pp. 471
    • Freeguard, G.F.1    Long, L.H.2
  • 6
    • 0000778261 scopus 로고
    • Brosted acid assisted chiral Lewis acid (BLA) catalyst for asymmetric Diels-Alder reaction
    • Ishihara, K.; Yamamoto, H. Brosted acid assisted chiral Lewis acid (BLA) catalyst for asymmetric Diels-Alder reaction. J. Am., Chem. Soc. 1994, 116, 1561.
    • (1994) J. Am., Chem. Soc. , vol.116 , pp. 1561
    • Ishihara, K.1    Yamamoto, H.2
  • 7
    • 0000656506 scopus 로고
    • A new chiral BLA promoter for asymmetric aza Diels-Alder and aldol-type reactions of imines
    • Ishihara, K.; Miyata, M.; Hattori, K.; Tada, T.; Yamamoto, H. A new chiral BLA promoter for asymmetric aza Diels-Alder and aldol-type reactions of imines. J. A. Chem. Soc. 1994, 116, 10520.
    • (1994) J. A. Chem. Soc. , vol.116 , pp. 10520
    • Ishihara, K.1    Miyata, M.2    Hattori, K.3    Tada, T.4    Yamamoto, H.5
  • 8
    • 0027246239 scopus 로고
    • Convenient method for the synthesis of chiral, -diphenyl-2- pyrrolidinemethanlol
    • Kanth, J. V.; Periasamy, M. Convenient method for the synthesis of chiral, -diphenyl-2-pyrrolidinemethanlol. Tetrahedron 1993, 49, 5127.
    • (1993) Tetrahedron , vol.49 , pp. 5127
    • Kanth, J.V.1    Periasamy, M.2
  • 9
    • 0037016937 scopus 로고    scopus 로고
    • A new catalytic enantioselective reducing reagent system from ( -)-α,α-diphenylpyrro-lidine-methanol and 9-borabicyclo[3.3.1]nonane, especially effective for hindered and substituted aralkylketones
    • Kanth, J. V. B.; Brown, H. C. A new catalytic enantioselective reducing reagent system from ( -)-α,α-diphenylpyrro-lidine-methanol and 9-borabicyclo[3.3.1]nonane, especially effective for hindered and substituted aralkylketones. Tetrahedron 2002, 58, 1069-1074.
    • (2002) Tetrahedron , vol.58 , pp. 1069-1074
    • Kanth, J.V.B.1    Brown, H.C.2
  • 10
    • 19044381229 scopus 로고    scopus 로고
    • Ph.D. Thesis, Wuhan University: Wuhan, in Chinese
    • 2 Symmetric Axis. Ph.D. Thesis, Wuhan University: Wuhan, 2003 (in Chinese).
    • (2003) 2 Symmetric Axis
    • Liu, D.J.1
  • 11
    • 0032573438 scopus 로고    scopus 로고
    • A simple convenient preparation for enantiometrically pure 1,1′-bi-2 naphthols
    • Shan, Z. X.; Xiong, Y.; Li, W. Z.; Zhao, D. J. A simple convenient preparation for enantiometrically pure 1,1′-bi-2 naphthols. Tetrahedron: Asymmetry 1998, 9 (22), 3985.
    • (1998) Tetrahedron: Asymmetry , vol.9 , Issue.22 , pp. 3985
    • Shan, Z.X.1    Xiong, Y.2    Li, W.Z.3    Zhao, D.J.4
  • 12
    • 0033605759 scopus 로고    scopus 로고
    • Resolution of racemic 1,1′-bi-2 naphthol using (S)-proline via a cyclic borate ester
    • Shan, Z. X.; Xiong, Y.; Zhao, D. J. Resolution of racemic 1,1′-bi-2 naphthol using (S)-proline via a cyclic borate ester. Tetrahedron 1999, 55, 3893.
    • (1999) Tetrahedron , vol.55 , pp. 3893
    • Shan, Z.X.1    Xiong, Y.2    Zhao, D.J.3
  • 13
    • 10844286786 scopus 로고    scopus 로고
    • A high-efficiency preparation, properties and structure of (R,S)- and (S,S)-pyrolidine-2-carboxylic acid 3,5-dioxa-4-boracyclohepta [2,1-a; 3,4-a′] dinaphthalen-4-yl esters
    • Shan, Z. X.; Liu, S. M.; Liu, D. J. A high-efficiency preparation, properties and structure of (R,S)- and (S,S)-pyrolidine-2-carboxylic acid 3,5-dioxa-4-boracyclohepta [2,1-a; 3,4-a′] dinaphthalen-4-yl esters. Chin. J. Chem. 2003, 21 (10), 1373.
    • (2003) Chin. J. Chem. , vol.21 , Issue.10 , pp. 1373
    • Shan, Z.X.1    Liu, S.M.2    Liu, D.J.3
  • 14
    • 0001728050 scopus 로고
    • New crystalline host based on tartaric acid. Synthesis, inclusion properties and X-ray structural characterization of interaction models with alcohol guests
    • Weber, E.; Dörpringhaus, N.; Wimmer, C. New crystalline host based on tartaric acid. Synthesis, inclusion properties and X-ray structural characterization of interaction models with alcohol guests. J. Org. Chem. 1992, 57, 6825.
    • (1992) J. Org. Chem. , vol.57 , pp. 6825
    • Weber, E.1    Dörpringhaus, N.2    Wimmer, C.3
  • 16
    • 10844297666 scopus 로고
    • (Chem. Abstr. 1986, 106, 179083).
    • (1986) Chem. Abstr. , vol.106 , pp. 179083


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.