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
来源：
TETRAHEDRON | 2002年 / 58卷 / 14期
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 [J].
Agami, C ;
Couty, F ;
Rabasso, N .
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 [J].
Agami, C ;
Couty, F ;
Rabasso, N .
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 [J].
AGAMI, C ;
COUTY, F ;
HAMON, L ;
VENIER, O .
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 [J].
Agami, C ;
Couty, F ;
Hamon, L ;
Venier, O .
JOURNAL OF ORGANIC CHEMISTRY, 1997, 62 (07) :2106-2112
[8]   1,2-amino alcohols and their heterocyclic derivatives as chiral auxiliaries in asymmetric synthesis [J].
Ager, DJ ;
Prakash, I ;
Schaad, DR .
CHEMICAL REVIEWS, 1996, 96 (02) :835-875
[9]   NEW ROUTES TO 1,4-BENZODIAZEPIN-2,5-DIONES [J].
AKSSIRA, M ;
BOUMZEBRA, M ;
KASMI, H ;
DAHDOUH, A ;
ROUMESTANT, ML ;
VIALLEFONT, P .
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
12345678910