The reactivity of the N-Boc protecting group:: an underrated feature

被引:110
作者
Agami, C [1 ]
Couty, F [1 ]
机构
[1] Univ Paris 06, CNRS, Lab Synth Asymetr, UMR 7611, F-75005 Paris, France
关键词
protecting groups; cyclisations; oxazolidinones; imidazolidinones; carbamates; inversion reactions; Thorpe-Ingold effect; peptides;
D O I
10.1016/S0040-4020(02)00131-X
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
[No abstract available]
引用
收藏
页码:2701 / 2724
页数:24
相关论文
共 121 条
  • [1] AGAMI A, 1995, SYNLETT, P1027
  • [2] AGAMI C, 1995, B SOC CHIM FR, V132, P808
  • [3] N-Boc-2-acyl oxazolidine methodology combined with ring-closing metathesis:: a new approach towards the enantioselective synthesis of α-(1-hydroxyalkyl) nitrogen heterocycles
    Agami, C
    Couty, F
    Rabasso, N
    [J]. TETRAHEDRON, 2001, 57 (25) : 5393 - 5401
  • [4] Agami C, 1996, SYNLETT, P511
  • [5] Synthesis of (-)-β conhydrine and analogues using N-Boc-2-acyl oxazolidine methodology and ring closing metathesis
    Agami, C
    Couty, F
    Rabasso, N
    [J]. TETRAHEDRON LETTERS, 2000, 41 (21) : 4113 - 4116
  • [6] CHIRAL OXAZOLIDINONES FROM N-BOC DERIVATIVES OF BETA-AMINO ALCOHOLS - EFFECT OF A N-METHYL SUBSTITUENT ON REACTIVITY AND STEREOSELECTIVITY
    AGAMI, C
    COUTY, F
    HAMON, L
    VENIER, O
    [J]. TETRAHEDRON LETTERS, 1993, 34 (28) : 4509 - 4512
  • [7] Regio- and stereocontrolled formation of chiral epoxy oxazolidines via bromocarbamation of N-Boc alkenyl oxazolidines. Application to asymmetric synthesis
    Agami, C
    Couty, F
    Hamon, L
    Venier, O
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 1997, 62 (07) : 2106 - 2112
  • [8] 1,2-amino alcohols and their heterocyclic derivatives as chiral auxiliaries in asymmetric synthesis
    Ager, DJ
    Prakash, I
    Schaad, DR
    [J]. CHEMICAL REVIEWS, 1996, 96 (02) : 835 - 875
  • [9] NEW ROUTES TO 1,4-BENZODIAZEPIN-2,5-DIONES
    AKSSIRA, M
    BOUMZEBRA, M
    KASMI, H
    DAHDOUH, A
    ROUMESTANT, ML
    VIALLEFONT, P
    [J]. TETRAHEDRON, 1994, 50 (30) : 9051 - 9060
  • [10] Albericio F, 2000, BIOPOLYMERS, V55, P123, DOI 10.1002/1097-0282(2000)55:2<123::AID-BIP30>3.0.CO