PMID- 26843100
OWN - NLM
STAT- PubMed-not-MEDLINE
DCOM- 20160624
LR  - 20160219
IS  - 1523-7052 (Electronic)
IS  - 1523-7052 (Linking)
VI  - 18
IP  - 4
DP  - 2016 Feb 19
TI  - Approach to Isoindolinones, Isoquinolinones, and THIQs via Lewis Acid-Catalyzed 
      Domino Strecker-Lactamization/Alkylations.
PG  - 634-7
LID - 10.1021/acs.orglett.5b03331 [doi]
AB  - A one-pot, three-component synthesis of widely substituted isoindolinones and 
      isoquinolinones, featuring a Lewis acid-catalyzed efficient Strecker reaction and 
      lactamization sequence, affording products in good to high yields is reported. 
      The method has also been extended to the synthesis of tetrahydroisoquinolines 
      (THIQs) in high yields.
FAU - Dhanasekaran, Sivasankaran
AU  - Dhanasekaran S
AD  - Department of Chemistry, Indian Institute of Technology , Kanpur, UP - 208 016, 
      India.
FAU - Suneja, Arun
AU  - Suneja A
AD  - Department of Chemistry, Indian Institute of Science Education and Research , 
      Bhopal, MP - 462 066, India.
FAU - Bisai, Vishnumaya
AU  - Bisai V
AD  - Department of Chemistry, Indian Institute of Science Education and Research , 
      Bhopal, MP - 462 066, India.
FAU - Singh, Vinod K
AU  - Singh VK
AD  - Department of Chemistry, Indian Institute of Science Education and Research , 
      Bhopal, MP - 462 066, India.
AD  - Department of Chemistry, Indian Institute of Technology , Kanpur, UP - 208 016, 
      India.
LA  - eng
PT  - Journal Article
PT  - Research Support, Non-U.S. Gov't
DEP - 20160204
PL  - United States
TA  - Org Lett
JT  - Organic letters
JID - 100890393
EDAT- 2016/02/05 06:00
MHDA- 2016/02/05 06:01
CRDT- 2016/02/05 06:00
PHST- 2016/02/05 06:00 [entrez]
PHST- 2016/02/05 06:00 [pubmed]
PHST- 2016/02/05 06:01 [medline]
AID - 10.1021/acs.orglett.5b03331 [doi]
PST - ppublish
SO  - Org Lett. 2016 Feb 19;18(4):634-7. doi: 10.1021/acs.orglett.5b03331. Epub 2016 
      Feb 4.