vinylmagnesium bromide

C=CC(O)[C@H](CC(C)C)NC(=O)OC(C)(C)C
Reaction #4352
desired product
المردود 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
C=CC(O)(CCC(C)C)[C@H](CC(C)C)NS(=O)(=O)c1ccccc1C
Reaction #4354
desired product
المردود 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
C=CC(O)C(CC(C)C)NC(=O)OC(C)(C)C
Reaction #4355
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
C=CC(C)(O)CCC=C(C)CCC=C(C)COC1CCCCO1
Reaction #5757
3,7,11-trimethyl-12-(2-tetrahydropyranyl)oxy-1,6,10-dodecatrien-3-ol
المردود 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CC(C)(O)CCC=C(C)CCC=C(C)COCOC
Reaction #5758
3,7,11-trimethyl-12-(methoxymethyl)oxy-1,6,10-dodecatrien-3-ol
المردود 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CCC(CC=C)c1c(-c2ccccc2)c(C)c(C#N)c2nc(C3CC3)oc12
Reaction #45866
compound
المردود 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Clc1ccc2cc[nH]c2c1Cl
Reaction #46781
expected compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Clc1nccc2cc[nH]c12
Reaction #48484
7-chloro-6-azaindole
المردود 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCC[C@@H]1CO1
Reaction #69931
(R)-1,2-Epoxyhexane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C=CC(NS(=O)C(C)(C)C)C1(c2ccc(F)cc2)CCC2(CC1)OCCO2
Reaction #73477
( 106 )
المردود 50.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C=CC(O)(C=C)CC[C@H](O)COC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #75598
(2S)-1-(trityloxy)-5-vinyl-6-heptene-2,5-diol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
C=CC1(O)CN2CCC1CC2
Reaction #76782
title compound
المردود 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
C=CC1(O)CN2CCC1CC2
Reaction #77879
title compound
المردود 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
C=CC(C)(O)c1cc(Cl)ccc1Cl
Reaction #82518
3-hydroxy-3-(2,5-dichlorophenyl)-1-butene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
C=CC(=O)[C@H](CC1CCCC1)NC(=O)OC(C)(C)C
Reaction #87119
(S)-tert-butyl (1-cyclopentyl-3-oxopent-4-en-2-yl)carbamate
المردود 38.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C=CC[C@@H](O)COCc1ccccc1
Reaction #155568
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=CC[C@H](O)C(c1ccccc1)c1ccccc1
Reaction #166100
(2S)-1,1-diphenyl-pent-4-ene-2-ol
المردود 70.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=CC[C@@H](O)C(c1ccccc1)c1ccccc1
Reaction #166101
(2R)-1,1-diphenyl-pent-4-ene-2-ol
المردود 694.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=CC(NC(=O)OC(C)(C)C)(c1cccc(Br)c1)C(F)F
Reaction #168716
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=CC(=O)[C@H](Cc1cc(F)cc(F)c1)NC(=O)OC(C)(C)C
Reaction #219979
vinyl ketone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
الصفحة 1التالي